Abstract
Owing to its high disability and mortality rates, stroke has been the second leading cause of death worldwide. Since the pathological mechanisms of stroke are not fully understood, there are few clinical treatment strategies available with an exception of tissue plasminogen activator (tPA), the only FDA-approved drug for the treatment of ischemic stroke. Angiogenesis is an important protective mechanism that promotes neural regeneration and functional recovery during the pathophysiological process of stroke. Thus, inducing angiogenesis in the peri-infarct area could effectively improve hemodynamics, and promote vascular remodeling and recovery of neurovascular function after ischemic stroke. In this review, we summarize the cellular and molecular mechanisms affecting angiogenesis after cerebral ischemia registered in PubMed, and provide pro-angiogenic strategies for exploring the treatment of ischemic stroke, including endothelial progenitor cells, mesenchymal stem cells, growth factors, cytokines, non-coding RNAs, etc.
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Introduction
Stroke is the second leading cause of mortality and the leading cause of disability worldwide. It has high morbidity, mortality and disability rates, and its treatment methods are limited [1]. Stroke is a pathological condition that causes the cessation of blood supply to a portion of the brain, which results in abnormal blood dynamics, neurovascular function, and energy metabolism [2]. Ischemia or hemorrhage caused by a thrombus or systemic hypoperfusion can lead to the development of stroke [3]. Stroke is categorized into ischemic and hemorrhagic, wherein approximately 87% of cases are cerebral ischemia [4]. Currently, acute focal stroke is managed using three major approaches: neuroprotective, endovascular thrombectomy and thrombolytic therapy [3]. Theoretically, neuroprotection is a common strategy in treating ischemic and hemorrhagic stroke, and animal experimental models of stroke showed the effectiveness of neuroprotective drugs [5,6,7]. However, only a few have been proven clinically effective. Recent studies have shown that endovascular thrombectomy could improve recanalization rates in patients with ischemic stroke caused by large-artery occlusion, but surgical intervention could only be performed in select patients [8]. Additionally, the only FDA-approved drug for ischemic stroke treatment is tPA, which binds to fibrin via its lysine residue and activates the conversion of fibrinogen-bound plasminogen to plasmin, thereby achieving thrombolytic therapy [9]. However, its narrow therapeutic window (within 4.5 h after stroke) results in only 3%–5% of patients receiving timely treatment in practice, which hinders its better and broader clinical application [9]. Currently, no drugs can be used as a treatment for hemorrhagic stroke, which has a higher mortality rate [10]. Therefore, the pathological mechanism of stroke should be elucidated, and better drugs or methods should be available to treat stroke.
Neurovascular networks have been recently proposed, and the close communication between neurons and blood vessels is essential for brain function [11]. Certainly, angiogenesis is an important protective mechanism promoting nerve regeneration and functional recovery during stroke. Studies have shown that cerebral ischemia could induce transient angiogenesis [12]. Moreover, ischemic stroke treatment involves the promotion of angiogenesis in the peri-infarct area, which could effectively reduce the infarct volume, promote nerve cell survival and recover neurovascular network function [13]. With the development of stem cell technology and the discovery of molecular targets, cell and molecular therapies have been proposed, including stem cells such as endothelial progenitor cells (EPCs), mesenchymal stem cells (MSCs), and molecules such as vascular endothelial growth factor (VEGF), angiopoietin-1 (Ang1), microRNA, etc. This review summarized the cellular and molecular mechanisms affecting angiogenesis after cerebral ischemia in PubMed, and provided pro-angiogenic strategies to mainly explain ischemic stroke treatment, including EPCs, MSCs, growth factors, cytokines, non-coding RNAs (ncRNAs), etc.
Angiogenesis after ischemic stroke
The most basic requirement in embryonic development is the development of blood vessels, which takes precedence over the development and differentiation of other tissues and organs, and guarantees reproductive function, wound healing and tissue injury and repair in adults [14]. Neovascularization occurs via two main cellular processes: vasculogenesis and angiogenesis [15]. Vasculogenesis, occurring mostly during embryonic blood vessel formation, refers to the differentiation of undifferentiated precursor cells (angioblasts) into endothelial cells (ECs), which assemble into the primitive vascular network [14]. Angiogenesis refers to the growth of new vascular structures from existing blood vessels and involves various physiological and pathological processes in vivo, such as menstruation, pregnancy, wound healing, fracture repair, and “therapeutic angiogenesis” caused by ischemia [16]. More importantly, new blood vessels are mainly formed through angiogenesis in adults, although vasculogenesis has also been reported [3]. Angiogenesis has three main forms: remodeling of blood vessels to form smaller microvessels, sprouting angiogenesis, and arteriogenesis, which is the remedial formation of mature new arteries, increasing in length and width, from preexisting interconnected arterioles after arterial occlusion [17]. Evidence showed that angiogenesis after cerebral ischemia occurs through sprouting, which involves EC proliferation, migration, angiogenic sprouting and lumen formation, and endothelial network maturation [3] (Fig. 1).
a Pro-angiogenic molecules such as NO and VEGF induce local vasodilation, antagonize tight junctions between ECs, and initiate angiogenesis after ischemic stroke. Pericytes and smooth muscle cells are also loosened, resulting in extravasation of intravascular plasma proteins. b Activated ECs (graded pink) are induced to proliferate and migrate by a variety of angiogenic factors (VEGF, FGF, PDGF, αvβ3 integrin, etc.) to form subulate vascular buds. c Stimulated by VEGF, integrins (αvβ3 or α5) and other factors, activated EC continue to proliferate and migrate outwards, forming lumen with adjacent budding. d The newly formed lumen is not stable and needs to ensure endothelial cell survival and function, for example, tight junctions between ECs, orderly support of pericytes and smooth muscle cells, and deposition of the extracellular matrix.
After the development of stroke, the ischemic penumbra tissue releases a complex mix of angiogenic factors, such as VEGF, angiopoietins, platelet-derived growth factor (PDGF), angiogenin, transforming growth factors (TGFs), basic fibroblast growth factor (bFGF), matrix metalloproteinase (MMP), nitric oxide (NO), etc [18]. These angiogenic factors initiate and regulate angiogenesis, of which VEGF is a critical stimulator of angiogenesis. In humans, angiogenesis occurs 3–4 days after ischemic stroke [19]. Post-mortem analyses of stroke patients showed an increased cerebral blood vessel density in the peri-infarct region compared with the contralateral normal area [19]. Moreover, blood vessel density in the ischemic border correlates with survival in stroke patients, and those with greater cerebral blood vessel density have better survival [19].
Initiation of angiogenesis after ischemic stroke
As the primary effector cells of the angiogenic response, ECs surrounding the infarcted brain area start to proliferate as early as 12–24 h after the development of ischemic stroke [20]. Moreover, VEGF upregulation in the peri-infarct region was described as early as 3 h after an ischemic insult, indicating that angiogenesis was initiated within hours of stroke onset [21]. Upon onset of ischemia stroke, VEGF and NO increase vascular permeability, leading to plasma protein extravasation that forms a temporary scaffold for endothelial cell migration [17]. For ECs to migrate from their resident sites, the contacts between ECs are loosened, and the support of the surrounding cells (pericytes and smooth muscle cells) is weakened, which ultimately leads to vascular instability [17]. After ischemic stroke onset, the reactive astrocytes restructure the extracellular matrix (ECM), leading to the formation of ECM tracts that are used by migrating endothelial cells to establish new capillary buds [22, 23]. After establishing the sprouting path, VEGF binds to its receptors on vascular ECs to directly initiate an angiogenic response, promoting the proliferation and migration of endothelial cells [15].
Angiogenic sprouting after ischemic stroke
After initiation of angiogenesis, ECs are activated, which release proteases to degrade the ECM, and they proliferate and migrate to a distant space [3]. This process leads to vascular sprout formation, and depends on the involvement of various proteases and angiogenic cytokines, such as VEGF, placental growth factor (PLGF), Ang 1/2, FGF, PDGF, αvβ3 integrin, etc.
Lumen formation after ischemic stroke
After vessel sprouting, ECs accumulate continuously outward from the sprouting like solid cords, and the lumen is formed from the adjacent new budding [3]. Endothelial embedding and fusion with native vessels increase the vessel diameter and length in response to angiogenic factors, such as VEGF, Ang1, integrins (αvβ3 or α5), myocyte enhancer-binding factor 2 C, etc. Excessive matrix proteolysis may lead to cystic EC aggregation, which prevents lumen formation.
Maturation of the endothelial network after ischemic stroke
Endothelial network maturation includes the survival and differentiation of ECs in the neovascular lumen and vascular remodeling [24]. Studies showed that reduced endothelial cell survival led to vascular degeneration, which was detrimental to angiogenesis [17]. After the onset of ischemic stroke, ECs acquire special characteristics determined by the local tissue to adapt to the needs of the microenvironment [25]. For example, ECs involved in the exchange of substances in the endocrine glands differentiated into discontinuous and porous cells [26]. One of the most important parts of a mature endothelial network is remodeling, wherein new vessels are trimmed into capillary-like vessels that are organized irregularly into a structured branched vascular network [17]. Additionally, vascular smooth muscle cells and pericytes migrate around the blood vessels and contribute to ECM deposition. At this stage, various pro-angiogenic factors play an important role, such as VEGF, Ang and its receptor Tie, GTP-binding protein Gα13, cell adhesion molecules, chemokine receptor 4, integrin α4, etc.
Cellular regulation of angiogenesis after ischemic stroke
The vasculature in the brain originates from vasculogenesis during embryonic development and has some plasticity in adults. When cerebral ischemia occurs, various endogenous protective mechanisms are activated within a few minutes in the peri-infarct area, including angiogenesis, neurogenesis, glial cell infiltration, etc. After transient focal cerebral ischemia, a delayed increase was observed in cerebral blood flow and blood volume in the ipsilateral cortex, which may be related to angiogenesis [12]. Meanwhile, the cerebral ischemia-induced microvascular formation also promotes macrophage infiltration and clearance of necrotic tissue in the infarct area [13]. This enhanced angiogenesis in ischemic tissue is known as therapeutic angiogenesis. However, endogenous angiogenesis after ischemia was transient and completely disappeared weeks after ischemia. Endogenous angiogenesis was activated in the peri-infarct area in early cerebral ischemia [27]. Moreover, the remodeling area has different emerging progenitor cell populations [27, 28], such as EPCs, neural progenitor cells and oligodendrocyte progenitor cells (OPCs) [29]. Subsequently, evidence showed that various stem/progenitor cells had beneficial angiogenic effects [30], including embryonic stem cells (ESCs) [31], peripheral blood hematopoietic stem cells (CD34+) [32], mesenchymal stem cells [33], neural stem/progenitor cells [34], oligodendrocyte precursor cells [35], human umbilical cord blood cells (huCBCs) [36], skin-derived progenitor cells (SKPs) [37], and EPCs [29].
EPCs
In an observational case-control study on 100 stroke patients, including 50 lacunar strokes and 50 cortical strokes, circulating EPCs were identified as potential biomarkers for the diagnosis and prognosis of cerebral ischemia [38]. EPCs play an important role in adult angiogenesis [39]. In response to the pathophysiological needs of neovascularization, EPCs could be mobilized from the bone marrow into the peripheral blood and differentiated into functional ECs, which participate in the neovascularization and blood vessel repair and remodeling [29].
The upregulation of high-mobility group box 1 caused by reactive astrocytes could induce the activation and accumulation of endogenous EPCs [40], promoting angiogenesis through chemokine (C-X-C motif) receptor 4 (CXCR4)/stromal cell-derived factor-1 (SDF-1) axis [41]. Interestingly, the secretome of EPCs from stroke patients promotes angiogenesis and endothelial tightness, thereby preventing vascular leakage caused by ischemia [42]. Moreover, the mobilization of endogenous EPCs might be beneficial to the repair of cerebral ischemia.
Furthermore, several studies reported that intravenous administration of EPCs [43,44,45] or transplantation of bone marrow-derived EPCs [46] or endothelial colony-forming cells [47], a homogeneous EPC subtype, could effectively promote neovascularization and improve functional repair after acute focal cerebral ischemia. The mechanism may involve increased plasma VEGF levels [44] and upregulation of hypoxia-inducible factor (HIF-1α) signaling [45], which reduce blood-brain barrier (BBB) leakage and degradation of tight junction proteins. Moreover, EPC transplantation induces vascular remodeling, which is related to MMP9 in the brain [48]. EPC-derived exosomes increase CD31 and VEGF expressions to promote angiogenesis and improve cerebral ischemic injury [49] (Table 1). Furthermore, a single EPC injection could prolong the lifespan of stroke-prone spontaneously hypertensive rats [50]. Additionally, EPCs played a role in promoting angiogenesis in a mouse model of permanent cerebral ischemia [51]. The chemokine CXCL12 promoted endothelial cell migration and tube formation through its receptor CXCR4 [52]. Therefore, VEGF expression, endothelial cell proliferation, and tube formation increased more significantly, which increases vessel density, if EPCs overexpressing chemokine cxcl12 gene were used as a treatment for permanent damage caused by middle cerebral artery occlusion (MCAO) [51]. Although EPCs are the most important progenitor cells in angiogenesis, repair and remodeling after cerebral ischemia, and both endogenous EPC mobilization and exogenous EPC transplantation were effective, the exact mechanism has not been fully elucidated (Fig. 2).
After stroke, the administered stem cells arrived the peri-infarct area and not only replaced the injured cells by directly differentiating into the corresponding ECs, neural cells, etc., but also promoted angiogenesis in the ischemic area through a variety of mechanisms. Endothelial progenitor cells could not only directly increase HIF-1α signaling and plasma VEGF levels, but also increase CD31 and VEGF expression by secreting exosomes in the brain. MSCs could promote angiogenesis in many ways, such as transferring their functional mitochondria to stroke-damaged ECs through nanotubes, and activating the PI3K/Akt/eNOS signaling pathway by secreting exosomes to up-regulate the expression of microRNAs and angiogenic factors. And the expression and release of endogenous angiogenic factors such as VEGF/VEGFR, Ang-1/Tie-2 and EGF in the peri-infarct zone were also increased through Notch signaling. NPCs/NSCs and OPCs could promote angiogenesis by increasing tight junction proteins in brain capillaries through Ang-1/Tie2 and VEGF/VEGFR2 signaling pathways, and by promoting β-catenin in ECs through Wnt7a.
MSCs
MSCs, also known as bone marrow stromal cells (BMSCs), are a class of stem cells found primarily in the bone marrow, and they can differentiate into various cell types in vivo, including osteoblasts [53], adipocytes [54], chondrocytes [55], hepatocytes [56], astrocytes [57], neurons [58], etc. MSCs can cross the BBB without damaging the brain’s structural integrity [57], which has promoted the recent development of exogenous MSC transplantation in treating cerebral ischemia [33, 59]. Studies showed that intravenous administration of MSCs or human MSC cell line B10 in a rat model of focal cerebral ischemia could improve functional recovery by increasing the expression of neurotrophic factors, including insulin-like growth factor 1 (IGF-1), glial cell line-derived neurotrophic factor (GDNF), brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF), epidermal growth factor (EGF) and basic FGF [60, 61] (Table 1).
Moreover, the transplanted MSCs increase various pro-angiogenic factor expression through autocrine and paracrine effects, and induce neovascularization and stability in the ischemic region [62, 63]. Accumulating evidence showed that BMSC transplantation after cerebral ischemia promotes angiogenesis and increases the expression and release of endogenous angiogenic factors such as VEGF, Hes1, Ang1 and TGF-β1 in ischemic infarct areas through Notch signaling [64,65,66,67,68] (Fig. 2). MSC-induced vascular stabilization might be mediated by increased VEGF and Ang1 expression and their corresponding receptors Flk1 and Tie2 in mouse brain ECs or astrocytes [69]. Interestingly, systemically delivered MSCs could transfer their functional mitochondria to stroke-injured ECs via nanotubes, thereby improving endothelial cell function and saving the cerebrovascular system [70] (Table 1, Fig. 2). A study evaluating the time window of MSC treatment showed that MSC treatment might have a beneficial effect through angiogenic mechanisms in the late stage of permanent MCAO (at least >1 month) in rats [71]. This might be related to the survival, migration, homing and implantation of transplanted cells in the lesion area. Therefore, methods promoting recruitment, survival and enhanced function of MSC around the ischemic core have been proposed. For example, gene modification of delivered MSCs to overexpress PLGF [72], CCL2 [73], thrombospondin-4 (TSP4) [74], CXCR4 [75], or Ang-1 [76] further enhanced the angiogenesis function of MSCs. Hypoxia-pretreated BMSCs enhanced the survival, homing, migration and differentiation of BMSCs through CXCL12/CXCR4 signaling [77] or upregulating HIF-1α and growth trophic factors, such as BDNF, GDNF, VEGF, FIK-1, EPO, EPOR, SDF-1, and CXCR4 [78]. Similarly, mild hypothermia could induce homing and angiogenesis of transplanted BMSCs to promote functional recovery and significantly reduce infarct size [79]. Combined therapy with drugs could also promote the beneficial effect of MSC treatment. Icariin and MSCs synergistically promote angiogenesis after transient MCAO by significantly increasing VEGF and BDNF expressions by activating the PI3K and ERK1/2 pathways [80].
Recent studies showed that BMSCs release secretome and extracellular vesicles to effectively promote angiogenesis [81]. Conditioned medium experiments showed that secretome from human embryonic MSCs promotes the partial recovery of focal ischemic injury by improving angiogenesis [82]. Extracellular vesicles, including exosomes and microvesicles, are nanoscale vesicles [83]. Exosomes and microvesicles are 30–100 and 40–1000 nm in diameter, respectively [83]. Exosomes derived from BMSCs promote angiogenesis and improve endothelial cell injury in ischemic stroke mice by microRNA upregulation, such as miR-21-5p [84], miR-210 [85], and miR-126 [86]. Subsequently, it activated the PI3K/Akt/eNOS signaling pathway and induced the expression of pro-angiogenic factors, such as VEGF, VEGFR2, Ang1, Tie2, EGF, and PDGF [84,85,86] (Fig. 2). However, MSC-derived extracellular vesicles also improved cerebral angiogenesis and neurogenesis after stroke and prevented post-ischemic immunosuppression [87, 88] (Table 1). Gregorius et al. showed that the small extracellular vesicles produced by hypoxia-induced MSCs could promote cerebral vasculogenesis and brain remodeling in mice after focal cerebral ischemia by regulating miRNAs related to angiogenesis in human cerebral microvascular ECs, including up-regulation of miR-126-3p, miR-140-5p, and let-7C-5p, and the down-regulation of miR-186-5p, miR-370-3p, and miR-409-3p [89]. Moreover, microvesicles from MSCs treated with normal rat brain extract (NBE-MSC-MVs) and stroke-induced rat brain extract (SBE-MSC-MVs) were significantly better than untreated MSC-MVs in improving inflammation and enhancing angiogenesis and neurogenesis [90].
Neural stem cells
Neural stem cells (NSCs) are derived from neural tissue, and they can self-renew and differentiate into neurons, astrocytes and oligodendrocytes [91]. To enhance angiogenesis and repair damaged nerve tissue, endogenous NSCs proliferate, migrate, and differentiate into neurons and astrocytes in the hippocampus and cerebral cortex during ischemic brain injury [91]. Intravenous injection of neural progenitor/stem cells could promote Ang1/Tie2 and VEGF/VEGFR2 signaling pathways in brain capillaries, and increase tight junction proteins to facilitate angiogenesis [34, 92, 93] (Fig. 2). Moreover, OPC transplantation promotes angiogenesis and remodeling in ischemic stroke by acting on endothelial β-catenin through Wnt7a [35, 94] (Fig. 2).
Additional stem cells
Various experimental and clinical models showed the therapeutic effects of stem cell transplantation on brain injury, including ESCs, induced pluripotent stem cells (iPSCs), bone marrow-derived cells (BMDCs), NSCs, etc [95]. Systemic transplantation of ESCs or embryonic NSCs enhances endogenous endothelial cell proliferation to promote angiogenesis in the peri-infarct areas [31, 96]. iPSCs have been shown to derive different cell types to improve functional recovery after ischemia [97], and iPSC-derived MSCs could secrete extracellular vesicles that promote tube formation and angiogenesis by inhibiting signal transducer and activator of transcription-3 (STAT3)-dependent autophagy in ECs during brain ischemia [98] (Table 1). Bone marrow-derived mononuclear cells (BMMNCs) can differentiate into smooth muscle cells and ECs to promote arteriogenesis and angiogenesis in rats [99]. The mechanism may be mediated by cell-cell interaction mediated by endothelial gap junctions [100] and the chemokine receptor CCR2 [101]. Because BMMNCs are a rich source of human hematopoietic stem cells, peripheral blood stem cell (CD34+) transplantation for stroke has also been considered [102]. Shyu et al. showed that transplanted CD34+ cells increase β1 integrin expression to promote angiogenesis in chronic ischemic rats [32] (Table 1).
In addition, SKPs could secrete bFGF and VEGF in the ischemic zone to promote endogenous angiogenesis and NSC proliferation [37] (Table 1). Moreover, the mechanism by which adipose-derived stem cells promote cerebral vascular remodeling was exosomes secretion containing microRNA-181b-5p, which downregulated the expression of transient receptor potential melatonin 7 [103], and contributed to the migration length and tube extension in brain microvascular endothelial cells [104]. Other stem cells are also used in vascular remodeling and angiogenesis after cerebral ischemia, such as hUCBCs [36], human placental trophoblast progenitor cells [105] and human amniotic fluid stem cells [106].
With the development of stem cell culture technology, three-dimensional (3D) organ-like tissues, also known as organoids, provide promising models for studying organogenesis and disease [107]. An organoid is an in vitro 3D cellular cluster derived from ESCs or iPSCs that can self-renew and self-organize [108, 109]. Organoids may facilitate stem cell therapies because they contain stem and progenitor cells. Studies showed that the grafting of cerebral organoids into the mouse cortex could form functional vascular connections with the mouse cortex [110,111,112]. We also confirmed that cerebral organoid transplantation promoted neurogenesis, angiogenesis and neurological recovery in stroke rats [113]. Notably, because cerebral organoids contain various nerve cell types, their regulation mechanism in angiogenesis has not been fully clarified.
Pericytes
BMDCs promote angiogenesis after cerebral ischemia [114, 115]. However, the BMDC cell type supporting vascular remodeling after cerebral ischemia is still unclear. Kokovay et al. used GFP expression to trace the role of transplanted BMDCs in recipient mice, and found that BMDCs with vascular remodeling did not have endothelial cell markers, but expressed desmin and vimentin, which ultimately identified these cells as pericytes [115]. Pericytes may be derived from the bone marrow, and they are involved in vascular remodeling after cerebral ischemia [115]. Pericytes play an important role in the early and late stages of new blood vessel formation to help angiogenic sprouting and maintain the vascular lumen composed of ECs. Therefore, pericytes need to constantly communicate with ECs and exchange information [116]. PDGF receptor-β (PDGFRβ) was specifically expressed in pericytes around the infarction area in the rat MCAO model and gradually increased over time [117]. Meanwhile, PDGF-B expression is also upregulated in ECs in peri-infarct areas and further phosphorylates Akt in peripheral pericytes with high PDGFRβ expression [117]. PDGFRβ-Akt signaling in pericytes upregulates NGF and neurotrophin-3 expression, thereby improving neurovascular injury after stroke [117]. Ang1 secreted by pericytes also activates Tie2 on the surface of ECs and promotes BBB formation [116]. Furthermore, after cerebral ischemia, pericytes also express and secrete other pro-angiogenic factors, such as VEGF, TGFβ, angiopoietin, sphingosine-1-phosphate (S1P) and Notch signaling [21, 116, 118, 119] (Table 1). Subsequently, ECs regulate angiogenesis and ECM remodeling through STAT3 to improve long-term recovery after ischemic stroke [120].
Microglia
Microglia, macrophage-like cells residing in the central nervous system, have similar functions to macrophages, with two opposite phenotypes, M1 and M2. M1 microglia mainly secrete pro-inflammatory cytokines and exert a pro-inflammatory effect, whereas M2 microglia secrete anti-inflammatory cytokines to exert an anti-inflammatory effect [121]. Studies showed that perivascular microglia promote vascular collapse in the cerebral ischemic penumbra region [121, 122]. Subsequently, capillary-associated microglia control purine release through the PANX1 channel to regulate blood flow and vascular dilatation [123] (Table 1).
Furthermore, pretreatment of primary microglia with oxygen-glucose deprivation (OGD) or BV2 cell stimulation with interleukin-4 (IL-4) polarized them into the M2 phenotype and promoted angiogenesis and endothelial tube formation after ischemic stroke by secreting extracellular vesicles [124, 125]. The exosomes released from IL-4-polarized BV2 cells contain miRNA-26a to function [124], whereas hypoxia-induced microglia release vesicles enriched in TGF-β1 to stimulate Smad2/3 signaling from ECs to induce angiogenesis [125]. Additionally, microglia could secrete some pro-inflammatory cytokines, which increases VEGF expression in ECs, promotes the proliferation and migration of ECs and angiogenesis, including MCP-1, TGF-α, TGF-β, granulocyte colony-stimulating factor (G-CSF), FGF, IL-4, IL-6, IL-1β, etc [126] (Table 1).
Molecular regulation of angiogenesis after ischemic stroke
During and after cerebral ischemia, cerebral blood vessels become unstable, vascular cells become relaxed, and ECs gradually proliferate, migrate and sprout, and angiogenesis occurs [15]. In this series of processes, different cell types and molecules mediating the crosstalk between cells are involved. These molecules regulate the biological behavior of various cells in a complex and coordinated manner and influence angiogenesis after stroke. Meanwhile, each molecule regulating angiogenesis shows its unique regulation mode and function. These factors, including growth factors, cytokines, angiogenic mediators, microRNAs, etc., mediate endothelial cell proliferation and migration, as well as tube formation and stability.
Growth factors
Accumulating data showed the involvement of several growth factors in angiogenesis after ischemic stroke, including bFGF, NGF, PDGF, BDNF, TGF-β1, and VEGF.
Mammals have five VEGF isoforms, such as VEGF-A, VEGF-B, VEGF-C, VEGF-D and PLGF, of which VEGF-A is the most original and most potent for angiogenesis [127]. VEGF-A acts via its receptors VEGFR1 and VEGFR2 in vascular ECs. Because of the low kinase activity of VEGFR1, VEGF-A angiogenesis is mainly achieved through its highly homologous VEGFR2 [128]. In 1996, two articles reported the importance of VEGF for embryonic angiogenesis [129, 130]. In 1998, a study showed that VEGF was significantly upregulated in the ischemic penumbra region after focal cerebral ischemia [131]. Mechanistically, HIF-1α and HIF-2α increased VEGF expression through ischemia or hypoxia [127, 132, 133] (Fig. 3). In addition, the transcriptional coactivator PGC-1α, independent of hypoxia response pathways and HIFs, strongly regulates VEGF expression and hindlimb angiogenesis in cultured muscle cells and skeletal muscle in vivo [134]. Moreover, specific p53 inhibition by pifithrin-α could lead to increased VEGF expression and angiogenesis after cerebral ischemia [135]. 15-Lipoxygenase (15-LO) catalyzes 15(S)-hydroxyeicosatetraenoic acid (15-HETE), major metabolite of arachidonic acid [136]. The 15-LO-1/15-HETE system was upregulated in cell models induced by OGD and a mouse model of MCAO, which also increased VEGF expression and promoted endothelial cell migration and microvessel formation after ischemic stroke [137] (Fig. 3). Endogenous VEGF was upregulated during or after cerebral ischemia to participate in angiogenesis through multiple different mechanisms. Therefore, exogenous administration of VEGF or in combination with indirect vasoreconstructive surgery could stimulate angiogenesis, reduce infarct size, and improve neurovascular function after chronic cerebral hypoperfusion [138, 139]. Furthermore, intraventricular injection of recombinant human VEGF also promotes pericyte coverage around the ECs and stabilizes neovascularization by increasing N-cadherin expression on cerebral capillaries [140] (Fig. 3). However, only a few studies support the mechanism of the VEGF/VEGFR cascade in regulating angiogenesis under the pathophysiological conditions of stroke. The combination of VEGF and Ang-2 leads to BBB leakage and promotes angiogenesis by increasing MMP-9 activity and inhibiting ZO-1 expression [141]. Interestingly, VEGF-B promotes the proliferation and differentiation of C2C12 myoblasts and skeletal muscle development through the PI3K/Akt signaling pathway regulated by VEGFR1 [142]. In VEGFR2-expressing neurons, PGC-1α increases VEGF expression and induces downstream PI3K/Akt and MEK/ERK signaling pathways to protect hippocampal neurons from apoptosis [143]. However, increased VEGF expression in OGD-induced ECs activates ERK signaling via its receptor Flk-1 but induces cell death [144] (Fig. 3), suggesting that the same signaling molecules mediate different effects in different cell types.
NGF promoted angiogenesis by activating p-focal adhesion kinase (FAK) or PI3K/Akt signaling pathways after ischemic stroke, and similar pathways had also been found in TSLP and its receptor TSLPR. IL-1α, TNF-1α and SDF-1α also promoted angiogenesis by activating the expression of downstream genes through their receptors, respectively.
In 1991, bFGF, a heparin-binding growth factor, was discovered, and bFGF intraventricular administration could promote cerebrovascular neovascularization after chronic cerebral ischemia [145]. Recent mechanistic studies found that intranasal administration of non-mitogenic FGF1 could activate the S1P receptor 1 (S1PR1) signaling pathway through its receptor FGFR1 and promote angiogenesis after stroke in vivo [146]. COX-2 expression is upregulated in in vitro cerebral microvascular ECs treated with bFGF, which promotes prostaglandin E2 (PGE2) production and increases VEGF expression in an autocrine manner [147] (Fig. 3). In addition, treadmill training increases bFGF expression in the ischemic brain, which further improves neurogenesis and angiogenesis through the caveolin-1/VEGF signaling pathway [148]. Interestingly, FGFR1 expression is up-regulated in intracerebral pericytes after cerebral ischemia or hypoxia [149]. With the administration of inhibitors, stroke-induced increased bFGF expression and upregulated PDGFRβ expression in pericytes of ischemic hemispheres by activating Akt/ERK signaling pathway via its receptor FGFR1, and improved BBB function after cerebral ischemia [149] (Fig. 3).
Angiogenesis after cerebral ischemia is also promoted by neurotrophins, originally found to induce neurogenesis, such as BDNF [150], hepatocyte growth factor [151], mesencephalic astrocyte-derived neurotrophic factor [152], PDGF [153], heparin-binding epidermal growth factor-like growth factor [154], TGF-β1 [155, 156], and growth differentiation factor 11 belonging the TGF-β superfamily and its downstream signaling molecule activin-like kinase 5 [157]. NGF also promotes angiogenesis by activating p-focal adhesion kinase (FAK) or PI3K/Akt signaling pathway after ischemic stroke [158, 159] (Fig. 3).
Cytokines
After the onset of stroke, cells, such as microglia and astrocytes are activated in the brain, and immune cells in the periphery, such as macrophages, also infiltrate into the brain, which releases cytokines, such as IL-8 [160], IL-6 [161], IL-1α [162], tumor necrosis factor-α (TNF-α) [163], galectin-3 (Gal-3) [164], Gal-1 [165], SDF-1α [166], G-CSF [167, 168], thymic stromal lymphopoietin (TSLP) [169], axon guidance factor netrin-1 [170, 171] and netrin-4 [172]. Although their mechanisms were different, these upregulated cytokines promote angiogenesis in ischemic brain regions.
Although IL-6 and IL-8 are members of the interleukin family, their mechanism of action is different. IL-8 promotes angiogenesis after ischemic stroke by increasing VEGF expression in human bone marrow MSCs via the PI3K/Akt and MAPK/ERK signaling pathways [160], whereas, IL-6 knockout decreases STAT3 activation and gene expression related to angiogenesis, such as Cxcl4, Thbs1, Anxa2 and Adamts1, leading to decreased vessel density [161]. Compared with IL-1β, IL-1α has more potential to induce endothelial cell activation after cerebral ischemia [162]. IL-1α increases CXCL-1 and IL-6 expression via its receptor IL-1R, and promotes the migration and proliferation of ECs and tube-like structure formation [162] (Fig. 3). In addition, TNF-α, another pro-inflammatory cytokine, upregulates α5β1 and αVβ3 integrin expression via tumor necrosis factor receptor 1 (TNFR1), inducing endothelial cell proliferation and angiogenesis [163] (Fig. 3). Moreover, TSLP activates the PI3K/Akt pathway in human umbilical vein endothelial cells via its receptor TSLPR to promote cell proliferation, migration and tube extension [169] (Fig. 3).
Gal-3, an important angiogenic cytokine, is mainly derived from activated microglia and astrocytes, and it infiltrates macrophages in the brain after ischemic stroke [173]. Increased Gal-3 expression induces integrin-linked kinase/p-Akt/ERK1/2 signaling to promote microglial migration and angiogenesis [164, 174]. SDF-1α has also been involved in the mobilization of hematopoietic stem cells from the bone marrow to the periphery [166]. Shyu et al. showed that intracerebral injection of SDF-1α increased the arrival of BMDCs to damaged brain areas and increased pro-angiogenic factor expression, such as VEGF, BDNF, and GDNF in peri-infarct areas [166]. SDF-1α overexpression with the adeno-associated virus in mouse models of MCAO also showed that SDF-1α activates Akt, ERK, and p38 pathway through its receptor CXCR4 but not JNK [175] (Fig. 3).
Angiogenic mediators
In addition to the above cytokines that directly promote endothelial cell proliferation and migration, many important signaling molecules, such as the Ang1-Tie2 signaling pathway [176], Jagged1-Notch1 signaling pathway [177], HIF-1α/VEGF, Nrf2/HO-1/eNOS, EPO/EPOR, integrin family systems, etc., mediate angiogenesis after cerebral ischemia.
Angiopoietin has been identified in four different subtypes, including Ang-1, Ang-2, Ang-3 and Ang-4, with Ang-1 and Ang-2 being the most widely studied [178]. Ang-1 mediates the proliferation, migration and survival of ECs and reduces BBB leakage through its tyrosine kinase receptor Tie-2 during angiogenesis [176, 179]. Moreover, estradiol and its receptor estrogen receptor-α increase Ang1 levels in the brain under basal conditions or in stroke-induced brain damage, further increasing capillary density [180]. In contrast, Ang2 antagonizes Tie2 and disrupts the connections between ECs, leading to cell death and vascular destruction [181]. However, Ang2 and VEGF induce BBB destruction and promote angiogenesis by increasing MMP-9 activity and inhibiting ZO-1 expression after cerebral ischemia [16, 141]. Angptl [182] and Angpt4 [183], members of the angiopoietin-related protein family, improve cerebral microvascular function after cerebral ischemia. Mechanically, Angpt4 maintains the integrity of the brain endothelial barrier by increasing the stability of the VEGFR2-VE-cadherin complex [183].
MMP9 overexpression or increased endogenous metalloproteinase membrane type 1-metalloprotease levels induced by treadmill exercise improves microvessel density after cerebral ischemia by degrading collagen IV, a major component of the basal lamina [184, 185]. Besides, Yang et al. found that MMPs damage the tight junction between ECs in early cerebral ischemia; thus, early inhibition of MMP may be beneficial to the recovery of BBB after stroke by affecting the expression of extraendothelial tight junction proteins, such as ZO-1 and claudin-5 associated with pericytes and astrocytes [186].
In addition, the expression of Notch1 and its ligands Jagged1 and delta-like ligand (DLL) significantly increases in the infarct area after cerebral ischemia [187]. Subsequently, the Notch intracellular domain in ECs dissociates from the cell membrane and translocates to the nucleus to form a complex with RBPJ protein to further activate the transcription of Notch target genes [177]. Our previous studies showed that nicotinamide phosphoribosyltransferase (NAMPT) stimulates angiogenesis after ischemic stroke [188]. Mechanistically, NAMPT, a key rate-limiting enzyme for NAD+ salvage synthesis, modulates DLL4/Notch signaling in endothelial progenitor cells via NAD+/SIRT1 in a mouse model of hind-limb ischemia [189].
Furthermore, more studies have shown that integrins such as β1, α5β1 and αvβ3 play important roles in regulating angiogenesis and inflammation after cerebral ischemia [190]. The strong upregulation of αvβ3, α5β1 and their ligand fibronectin in the ischemic penumbra stimulated the proliferation of vascular ECs [191], which was mediated by TNFR1 during ischemia-induced angiogenesis [192].
The most direct biochemical response of cerebral ischemia was inducing increased oxidative stress levels in the brain [193]. Additionally, reactive oxygen species derived from NADPH oxidase 2 regulate angiogenesis via the PI3K/Akt/NF-κB signaling pathway after focal cerebral ischemia [194]. Signaling molecules, such as HIF/VEGF [195] and Nrf2/HO-1, were associated with oxidative stress-related angiogenesis after stroke. Therefore, targeting these two signaling pathways was affected by many molecules, including Int6 [196], intelectin-1 [197], x‐box binding protein l splicing [198], PTEN [199], hemopexin [200], immunoproteasome subunit low molecular mass peptide 2 [201], sestrin2 [202], sphingosine kinase 1/S1P [203], C1q/LAIR1 [204], etc. Of these, Nrf2 activated by sestrin2 could also regulate the interaction between p62 and Keap1 by increasing p62 expression to induce angiogenesis after ischemic stroke [205]. Furthermore, erythropoietin (Epo) regulates HIF-1α and eNOS expression by activating the AMPK-KLF2 signaling pathway through its receptor Epo-R to promote the development of new blood vessels after ischemia in vitro and in vivo [206,207,208]. Exogenous supplementation of NO also mediates angiogenesis in the ischemic brain through the cGMP and VEGF pathways [209]. Similarly, H2S activates the PI3K/Akt signaling pathway, which stimulates the expression and release of VEGF and Ang1 in astrocytes and promotes the proliferation and migration of ECs and lumen formation after cerebral ischemia [210].
Recent studies showed that the metabolic level in the brain changed in a cascade manner after cerebral ischemia. In the infarcted penumbra, ischemia and hypoxia rapidly increased succinate levels, stimulated G protein-coupled receptor (GPR91) localized in neurons or astrocytes, and increased the expression of pro-angiogenic factors, such as VEGF, Ang1, IL-6, and IL-1β, through PGE2 and its receptor EP4 [211]. In addition, the administration of recombinant pyruvate kinase isoform M2 improves angiogenesis after cerebral ischemia by upregulating STAT3 and FAK expression [212]. Therefore, the changes in metabolic levels affected by cerebral ischemia may explain the progress of angiogenesis from the perspective of metabolism.
The following other molecules also regulate angiogenesis after cerebral ischemia: estrogen [213], kallikrein [214,215,216], endostatin [217], leptin [218], leucine‑rich‑α2‑glycoprotein 1 [219], developmental endothelial locus-1 [220], TSP-1 and TSP-2 [221], src and src-suppressed C kinase substrate [222], adiponectin [223], endothelin B receptor [224], sonic hedgehog [225,226,227], vasoactive intestinal peptide [228], TRPM4 [229], transient receptor potential cation channel subfamily V member 4 [230], pentraxin 3 [231], prostaglandin E1 [232], repulsive guidance molecule a [233], guanosine [234], prostaglandin‐endoperoxide synthase [235], glucagon-like peptide 1 [236], ephrinB2 [237], SorCS2 [238], mast cell‐expressed membrane protein 1 [239], CELSR1 [240], c-type lectin family 14 member A [241], apelin-13 [242], thrombomodulin [243], RTN4/S1PR2 [244], lactate and GPR81 [245], GPR124 [246], and histamine H 3 receptor [247].
ncRNAs
Recently, ncRNAs were identified [248], and studies showed alteration of ncRNA levels during or after stroke, which also affected angiogenesis [249]. ncRNA, including microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs), are functional RNA molecules that regulate the expression and function of different genes through different mechanisms [250, 251]. Of these, miRNAs and lncRNAs have been studied the most and were recently found to regulate angiogenesis after cerebral ischemia by affecting the levels of angiogenesis factors (Table 2).
Perspective
The brain is one of the most heavily perfused organs in the body. Almost every neuron has its own independent supply of blood vessels [252], suggesting a subtle relationship between neurons and blood vessels, known as the neurovascular network [253]. Blood vessels carry oxygen, energy, and nutrients to nourish neurons for proper function. Subsequently, blood vessels carry the waste neurons release, a series of physiological processes contributing to healthy brain function. Thus, previous therapies aimed solely at neuroprotection for stroke have become inadvisable.
Because of the importance of blood vessels in neurovascular units, angiogenesis in the treatment of cerebral ischemia has been considered and recognized. Nerve cells including NSCs and microglia, promote angiogenesis through multiple mechanisms, and angiogenesis also improves the interaction between neurons and glial cells during and after stroke. Thus, it promotes neurogenesis and improves nerve function. By contrast, providing nutritional support to the nerves is beneficial for glial cells [254].
Although this review summarized several roles and mechanisms in regulating angiogenesis after cerebral ischemia, most of them have not been fully explained, and several therapeutic approaches for inducing angiogenesis have limitations. The use of anti-VEGF/VEGFR drugs is popular in cancer treatment, with multiple FDA-approved drugs, such as bevacizumab, sorafenib, sunitinib, pazopanib, ramucirumab, lenvatini, fruquintini, anlotinib hydrochloride, etc [255, 256]. Although single molecular target drugs have shown significant efficacy in experimental animal models, they are not ideal for cerebral ischemia treatment because stroke is a complex disease. Therefore, molecular targets combined with cell therapy have been proposed and studied, such as CXCL12 gene overexpression in EPCs [51], and Ang-1, PIGF, TSP4, CCL2 or CXCR4 gene overexpression in MSCs [72,73,74,75,76]. Studies are still ongoing for the clinical application of novel microRNAs and lncRNAs.
Cell therapy is relatively superior compared with molecular targets. After reaching the peri-infarct area, the administered stem/progenitor cells could rescue or replace some of the injured cells to perform some functions, such as promoting angiogenesis, protecting neurons, and maintaining BBB homeostasis [33]. Otherwise, the injected stem/progenitor cells release secretome and extracellular vesicles to apply their pro-angiogenic effects. MSC-derived extracellular vesicles can induce the repair of ischemic stroke by upregulating the expression of various pro-angiogenic factors, such as VEGF, EGF, PDGF, Ang1, microRNA, etc [81, 88]. Although stem cell therapy is being investigated in clinical trials worldwide, several issues remain. Cell therapy requires several criteria, including the selection of which stem or progenitor cells (EPCs, MSCs, NPCs/NSCs, etc.) are better for treating stroke; the determination of the therapeutic window and the degree or stage of cerebral ischemia that is suitable for cell therapy; and the determination of the dosage, methods, and time of administration of cell therapy in clinical practice. In animal experiments, MSC transplantation therapy has different delivery methods, including intraventricular stereoscopic injection [257], intravenous injection [258], intra-arterial injection [259], and intranasal injection [260]. Furthermore, whether animal and clinical trials can be better matched remains to be resolved. Thus, some issues for cell therapy should be identified and resolved.
More importantly, the survival of cell transplantation is a key issue that needs attention and consideration of its therapeutic potential. With the development of materials science, biomaterials combined with cell therapy enhance the survival and differentiation of transplanted stem cells and improve neurological function in experimental stroke [261]. For example, hydrogel materials could serve as matrix mimics, such that temporary ECM is provided when placed in the peri-infarct area to enhance endogenous repair mechanisms [262]. Moreover, NPC transplantation with hydrogel/heparin/hyaluronan promotes the survival of NPCs and reduces inflammatory infiltration after transplantation [263]. Furthermore, the emergence of organoid technology has also promoted cell transplantation to a new level. Organoids consist of organ-specific stem/progenitor cells and mature cells that exhibit similar organ functionality as the tissue of origin [264]. Compared with transplants of dissociated NPCs, transplanted cerebral organoid exhibits enhanced cell survival and robust vascularization after ischemic stroke [110,111,112]. However, these are still experimental, and further clinical applications are worth looking forward to.
Conclusions
We reviewed several physiological and pharmacological pathways and potential mechanisms of the regulation of angiogenesis after cerebral ischemia. However, we lack a detailed understanding of potential treatment strategies for ischemic brain injury and their limitations. In the future, the underlying mechanisms of angiogenesis, as well as neurovascular units after stroke, should be explored.
References
Feigin VL, Brainin M, Norrving B, Martins S, Sacco RL, Hacke W, et al. World Stroke Organization (WSO): Global Stroke Fact Sheet 2022. Int J Stroke. 2022;17:18–29.
Silver JR. A history of Stoke Mandeville Hospital and the National Spinal Injuries Centre. J R Coll Physicians Edinb. 2019;49:328–35.
Chen YC, Wu JS, Yang ST, Huang CY, Chang C, Sun GY, et al. Stroke, angiogenesis and phytochemicals. Front Biosci (Sch Ed). 2012;4:599–610.
Tsao CW, Aday AW, Almarzooq ZI, Alonso A, Beaton AZ, Bittencourt MS, et al. Heart disease and stroke statistics-2022 update: a report from the American Heart Association. Circulation. 2022;145:e153–e639.
Yoshida H, Yanai H, Namiki Y, Fukatsu-Sasaki K, Furutani N, Tada N. Neuroprotective effects of edaravone: a novel free radical scavenger in cerebrovascular injury. CNS Drug Rev. 2006;12:9–20.
Wang XX, Wang F, Mao GH, Wu JC, Li M, Han R, et al. NADPH is superior to NADH or edaravone in ameliorating metabolic disturbance and brain injury in ischemic stroke. Acta Pharmacol Sin. 2022;43:529–40.
Liu XQ, Sheng R, Qin ZH. The neuroprotective mechanism of brain ischemic preconditioning. Acta Pharmacol Sin. 2009;30:1071–80.
Hankey GJ. Stroke. Lancet. 2017;389:641–54.
Marler JR, Goldstein LB. Medicine. Stroke–tPA and the clinic. Science. 2003;301:1677.
Wang P, Miao CY. NAMPT as a therapeutic target against stroke. Trends Pharmacol Sci. 2015;36:891–905.
Schaeffer S, Iadecola C. Revisiting the neurovascular unit. Nat Neurosci. 2021;24:1198–209.
Lin TN, Sun SW, Cheung WM, Li F, Chang C. Dynamic changes in cerebral blood flow and angiogenesis after transient focal cerebral ischemia in rats. Evaluation with serial magnetic resonance imaging. Stroke. 2002;33:2985–91.
Manoonkitiwongsa PS, Jackson-Friedman C, McMillan PJ, Schultz RL, Lyden PD. Angiogenesis after stroke is correlated with increased numbers of macrophages: the clean-up hypothesis. J Cereb Blood Flow Metab. 2001;21:1223–31.
Cleaver O. Mouse models of vascular development and disease. Curr Opin Hematol. 2021;28:179–88.
Liu J, Wang Y, Akamatsu Y, Lee CC, Stetler RA, Lawton MT, et al. Vascular remodeling after ischemic stroke: mechanisms and therapeutic potentials. Prog Neurobiol. 2014;115:138–56.
Fan Y, Yang GY. Therapeutic angiogenesis for brain ischemia: a brief review. J Neuroimmune Pharmacol. 2007;2:284–9.
Carmeliet P. Mechanisms of angiogenesis and arteriogenesis. Nat Med. 2000;6:389–95.
Beck H, Plate KH. Angiogenesis after cerebral ischemia. Acta Neuropathol. 2009;117:481–96.
Krupinski J, Kaluza J, Kumar P, Kumar S, Wang JM. Role of angiogenesis in patients with cerebral ischemic stroke. Stroke. 1994;25:1794–8.
Yang Y, Torbey MT. Angiogenesis and blood-brain barrier permeability in vascular remodeling after stroke. Curr Neuropharmacol. 2020;18:1250–65.
Marti HJ, Bernaudin M, Bellail A, Schoch H, Euler M, Petit E, et al. Hypoxia-induced vascular endothelial growth factor expression precedes neovascularization after cerebral ischemia. Am J Pathol. 2000;156:965–76.
del Zoppo GJ, Mabuchi T. Cerebral microvessel responses to focal ischemia. J Cereb Blood Flow Metab. 2003;23:879–94.
Iadecola C. The pathobiology of vascular dementia. Neuron. 2013;80:844–66.
Carmeliet P. Angiogenesis in health and disease. Nat Med. 2003;9:653–60.
Risau W. Development and differentiation of endothelium. Kidney Int Suppl. 1998;67:S3–6.
Maniotis AJ, Folberg R, Hess A, Seftor EA, Gardner LM, Pe’er J, et al. Vascular channel formation by human melanoma cells in vivo and in vitro: vasculogenic mimicry. Am J Pathol. 1999;155:739–52.
Carmichael ST. Themes and strategies for studying the biology of stroke recovery in the poststroke epoch. Stroke. 2008;39:1380–8.
Ohab JJ, Fleming S, Blesch A, Carmichael ST. A neurovascular niche for neurogenesis after stroke. J Neurosci. 2006;26:13007–16.
Esquiva G, Grayston A, Rosell A. Revascularization and endothelial progenitor cells in stroke. Am J Physiol Cell Physiol. 2018;315:C664–C74.
Zhu SZ, Szeto V, Bao MH, Sun HS, Feng ZP. Pharmacological approaches promoting stem cell-based therapy following ischemic stroke insults. Acta Pharmacol Sin. 2018;39:695–712.
Nagai N, Kawao N, Okada K, Okumoto K, Teramura T, Ueshima S, et al. Systemic transplantation of embryonic stem cells accelerates brain lesion decrease and angiogenesis. Neuroreport. 2010;21:575–9.
Shyu WC, Lin SZ, Chiang MF, Su CY, Li H. Intracerebral peripheral blood stem cell (CD34+) implantation induces neuroplasticity by enhancing beta1 integrin-mediated angiogenesis in chronic stroke rats. J Neurosci. 2006;26:3444–53.
Li J, Zhang Q, Wang W, Lin F, Wang S, Zhao J. Mesenchymal stem cell therapy for ischemic stroke: A look into treatment mechanism and therapeutic potential. J Neurol. 2021;268:4095–107.
Tang Y, Wang J, Lin X, Wang L, Shao B, Jin K, et al. Neural stem cell protects aged rat brain from ischemia-reperfusion injury through neurogenesis and angiogenesis. J Cereb Blood Flow Metab. 2014;34:1138–47.
Kishida N, Maki T, Takagi Y, Yasuda K, Kinoshita H, Ayaki T, et al. Role of perivascular oligodendrocyte precursor cells in angiogenesis after brain ischemia. J Am Heart Assoc. 2019;8:e011824.
Rosenkranz K, Kumbruch S, Tenbusch M, Marcus K, Marschner K, Dermietzel R, et al. Transplantation of human umbilical cord blood cells mediated beneficial effects on apoptosis, angiogenesis and neuronal survival after hypoxic-ischemic brain injury in rats. Cell Tissue Res. 2012;348:429–38.
Mao D, Yao X, Feng G, Yang X, Mao L, Wang X, et al. Skin-derived precursor cells promote angiogenesis and stimulate proliferation of endogenous neural stem cells after cerebral infarction. Biomed Res Int. 2015;2015:945846.
Rakkar K, Othman O, Sprigg N, Bath P, Bayraktutan U. Endothelial progenitor cells, potential biomarkers for diagnosis and prognosis of ischemic stroke: protocol for an observational case-control study. Neural Regen Res. 2020;15:1300–7.
Takizawa S, Nagata E, Nakayama T, Masuda H, Asahara T. Recent progress in endothelial progenitor cell culture systems: potential for stroke therapy. Neurol Med Chir (Tokyo). 2016;56:302–9.
Hayakawa K, Pham LD, Katusic ZS, Arai K, Lo EH. Astrocytic high-mobility group box 1 promotes endothelial progenitor cell-mediated neurovascular remodeling during stroke recovery. Proc Natl Acad Sci USA. 2012;109:7505–10.
Mao L, Huang M, Chen SC, Li YN, Xia YP, He QW, et al. Endogenous endothelial progenitor cells participate in neovascularization via CXCR4/SDF-1 axis and improve outcome after stroke. CNS Neurosci Ther. 2014;20:460–8.
Loiola RA, Garcia-Gabilondo M, Grayston A, Bugno P, Kowalska A, Duban-Deweer S, et al. Secretome of endothelial progenitor cells from stroke patients promotes endothelial barrier tightness and protects against hypoxia-induced vascular leakage. Stem Cell Res Ther. 2021;12:552.
Fan Y, Shen F, Frenzel T, Zhu W, Ye J, Liu J, et al. Endothelial progenitor cell transplantation improves long-term stroke outcome in mice. Ann Neurol. 2010;67:488–97.
Kong Z, Hong Y, Zhu J, Cheng X, Liu Y. Endothelial progenitor cells improve functional recovery in focal cerebral ischemia of rat by promoting angiogenesis via VEGF. J Clin Neurosci. 2018;55:116–21.
Geng J, Wang L, Qu M, Song Y, Lin X, Chen Y, et al. Endothelial progenitor cells transplantation attenuated blood-brain barrier damage after ischemia in diabetic mice via HIF-1alpha. Stem Cell Res Ther. 2017;8:163.
Zhang ZG, Zhang L, Jiang Q, Chopp M. Bone marrow-derived endothelial progenitor cells participate in cerebral neovascularization after focal cerebral ischemia in the adult mouse. Circ Res. 2002;90:284–8.
Moubarik C, Guillet B, Youssef B, Codaccioni JL, Piercecchi MD, Sabatier F, et al. Transplanted late outgrowth endothelial progenitor cells as cell therapy product for stroke. Stem Cell Rev Rep. 2011;7:208–20.
Morancho A, Ma F, Barcelo V, Giralt D, Montaner J, Rosell A. Impaired vascular remodeling after endothelial progenitor cell transplantation in MMP9-deficient mice suffering cortical cerebral ischemia. J Cereb Blood Flow Metab. 2015;35:1547–51.
Huang R, Cheng TX, Lai XL. Mechanism of ischemic brain injury repair by endothelial progenitor cell-derived exosomes. Mol Med Rep. 2022;26:269.
Peng C, Dong XH, Liu JL, Tao YL, Xu CF, Wang LP, et al. A preventive injection of endothelial progenitor cells prolongs lifespan in stroke-prone spontaneously hypertensive rats. Clin Sci (Lond). 2018;132:1797–810.
Li Y, Chang S, Li W, Tang G, Ma Y, Liu Y, et al. cxcl12-engineered endothelial progenitor cells enhance neurogenesis and angiogenesis after ischemic brain injury in mice. Stem Cell Res Ther. 2018;9:139.
Janssens R, Struyf S, Proost P. The unique structural and functional features of CXCL12. Cell Mol Immunol. 2018;15:299–311.
Garg P, Mazur MM, Buck AC, Wandtke ME, Liu J, Ebraheim NA. Prospective review of mesenchymal stem cells differentiation into osteoblasts. Orthop Surg. 2017;9:13–9.
Chen Q, Shou P, Zheng C, Jiang M, Cao G, Yang Q, et al. Fate decision of mesenchymal stem cells: adipocytes or osteoblasts? Cell Death Differ. 2016;23:1128–39.
Yang Y, Lin H, Shen H, Wang B, Lei G, Tuan RS. Mesenchymal stem cell-derived extracellular matrix enhances chondrogenic phenotype of and cartilage formation by encapsulated chondrocytes in vitro and in vivo. Acta Biomater. 2018;69:71–82.
Christ B, Dollinger MM. The generation of hepatocytes from mesenchymal stem cells and engraftment into the liver. Curr Opin Organ Transpl. 2011;16:69–75.
Kopen GC, Prockop DJ, Phinney DG. Marrow stromal cells migrate throughout forebrain and cerebellum, and they differentiate into astrocytes after injection into neonatal mouse brains. Proc Natl Acad Sci USA. 1999;96:10711–6.
Azad TD, Veeravagu A, Steinberg GK. Neurorestoration after stroke. Neurosurg Focus. 2016;40:E2.
Zhu Y, Guan YM, Huang HL, Wang QS. Human umbilical cord blood mesenchymal stem cell transplantation suppresses inflammatory responses and neuronal apoptosis during early stage of focal cerebral ischemia in rabbits. Acta Pharmacol Sin. 2014;35:585–91.
Wakabayashi K, Nagai A, Sheikh AM, Shiota Y, Narantuya D, Watanabe T, et al. Transplantation of human mesenchymal stem cells promotes functional improvement and increased expression of neurotrophic factors in a rat focal cerebral ischemia model. J Neurosci Res. 2010;88:1017–25.
Sheikh AM, Yano S, Mitaki S, Haque MA, Yamaguchi S, Nagai A. A Mesenchymal stem cell line (B10) increases angiogenesis in a rat MCAO model. Exp Neurol. 2019;311:182–93.
Malgieri A, Kantzari E, Patrizi MP, Gambardella S. Bone marrow and umbilical cord blood human mesenchymal stem cells: state of the art. Int J Clin Exp Med. 2010;3:248–69.
Tse WT, Pendleton JD, Beyer WM, Egalka MC, Guinan EC. Suppression of allogeneic T-cell proliferation by human marrow stromal cells: implications in transplantation. Transplantation. 2003;75:389–97.
Bao X, Feng M, Wei J, Han Q, Zhao H, Li G, et al. Transplantation of Flk-1+ human bone marrow-derived mesenchymal stem cells promotes angiogenesis and neurogenesis after cerebral ischemia in rats. Eur J Neurosci. 2011;34:87–98.
Guo F, Lv S, Lou Y, Tu W, Liao W, Wang Y, et al. Bone marrow stromal cells enhance the angiogenesis in ischaemic cortex after stroke: involvement of notch signalling. Cell Biol Int. 2012;36:997–1004.
Yang Z, Cai X, Xu A, Xu F, Liang Q. Bone marrow stromal cell transplantation through tail vein injection promotes angiogenesis and vascular endothelial growth factor expression in cerebral infarct area in rats. Cytotherapy. 2015;17:1200–12.
Moisan A, Favre I, Rome C, De Fraipont F, Grillon E, Coquery N, et al. Intravenous injection of clinical grade human MSCs after experimental stroke: functional benefit and microvascular effect. Cell Transpl. 2016;25:2157–71.
Ma XL, Liu KD, Li FC, Jiang XM, Jiang L, Li HL. Human mesenchymal stem cells increases expression of α-tubulin and angiopoietin 1 and 2 in focal cerebral ischemia and reperfusion. Curr Neurovasc Res. 2013;10:103–11.
Zacharek A, Chen J, Cui X, Li A, Li Y, Roberts C, et al. Angiopoietin1/Tie2 and VEGF/Flk1 induced by MSC treatment amplifies angiogenesis and vascular stabilization after stroke. J Cereb Blood Flow Metab. 2007;27:1684–91.
Liu K, Guo L, Zhou Z, Pan M, Yan C. Mesenchymal stem cells transfer mitochondria into cerebral microvasculature and promote recovery from ischemic stroke. Microvasc Res. 2019;123:74–80.
Komatsu K, Honmou O, Suzuki J, Houkin K, Hamada H, Kocsis JD. Therapeutic time window of mesenchymal stem cells derived from bone marrow after cerebral ischemia. Brain Res. 2010;1334:84–92.
Liu H, Honmou O, Harada K, Nakamura K, Houkin K, Hamada H, et al. Neuroprotection by PlGF gene-modified human mesenchymal stem cells after cerebral ischaemia. Brain. 2006;129:2734–45.
Lee S, Kim OJ, Lee KO, Jung H, Oh SH, Kim NK. Enhancing the therapeutic potential of CCL2-overexpressing mesenchymal stem cells in acute stroke. Int J Mol Sci. 2020;21:7795.
Zhang Q, Zhou ML, Wu XF, Li Z, Liu B, Gao WB, et al. Promoting therapeutic angiogenesis of focal cerebral ischemia using thrombospondin-4 (TSP4) gene-modified bone marrow stromal cells (BMSCs) in a rat model. J Transl Med. 2019;17:111.
Yu X, Chen D, Zhang Y, Wu X, Huang Z, Zhou H, et al. Overexpression of CXCR4 in mesenchymal stem cells promotes migration, neuroprotection and angiogenesis in a rat model of stroke. J Neurol Sci. 2012;316:141–9.
Onda T, Honmou O, Harada K, Houkin K, Hamada H, Kocsis JD. Therapeutic benefits by human mesenchymal stem cells (hMSCs) and Ang-1 gene-modified hMSCs after cerebral ischemia. J Cereb Blood Flow Metab. 2008;28:329–40.
Hu Y, Chen W, Wu L, Jiang L, Qin H, Tang N. Hypoxic preconditioning improves the survival and neural effects of transplanted mesenchymal stem cells via CXCL12/CXCR4 signalling in a rat model of cerebral infarction. Cell Biochem Funct. 2019;37:504–15.
Wei L, Fraser JL, Lu ZY, Hu X, Yu SP. Transplantation of hypoxia preconditioned bone marrow mesenchymal stem cells enhances angiogenesis and neurogenesis after cerebral ischemia in rats. Neurobiol Dis. 2012;46:635–45.
Bi M, Wang J, Zhang Y, Li L, Wang L, Yao R, et al. Bone mesenchymal stem cells transplantation combined with mild hypothermia improves the prognosis of cerebral ischemia in rats. PLoS One. 2018;13:e0197405.
Liu D, Ye Y, Xu L, Yuan W, Zhang Q. Icariin and mesenchymal stem cells synergistically promote angiogenesis and neurogenesis after cerebral ischemia via PI3K and ERK1/2 pathways. Biomed Pharmacother. 2018;108:663–9.
Shi Y, Shi H, Nomi A, Lei-Lei Z, Zhang B, Qian H. Mesenchymal stem cell-derived extracellular vesicles: a new impetus of promoting angiogenesis in tissue regeneration. Cytotherapy. 2019;21:497–508.
Asgari Taei A, Nasoohi S, Hassanzadeh G, Kadivar M, Dargahi L, Farahmandfar M. Enhancement of angiogenesis and neurogenesis by intracerebroventricular injection of secretome from human embryonic stem cell-derived mesenchymal stem cells in ischemic stroke model. Biomed Pharmacother. 2021;140:111709.
Tricarico C, Clancy J, D’Souza-Schorey C. Biology and biogenesis of shed microvesicles. Small GTPases. 2017;8:220–32.
Hu H, Hu X, Li L, Fang Y, Yang Y, Gu J, et al. Exosomes derived from bone marrow mesenchymal stem cells promote angiogenesis in ischemic stroke mice via upregulation of MiR-21-5p. Biomolecules. 2022;12:883.
Zhang H, Wu J, Wu J, Fan Q, Zhou J, Wu J, et al. Exosome-mediated targeted delivery of miR-210 for angiogenic therapy after cerebral ischemia in mice. J Nanobiotechnol. 2019;17:29.
Pan Q, Wang Y, Lan Q, Wu W, Li Z, Ma X, et al. Exosomes derived from mesenchymal stem cells ameliorate hypoxia/reoxygenation-injured ECs via transferring MicroRNA-126. Stem Cells Int. 2019;2019:2831756.
Doeppner TR, Herz J, Gorgens A, Schlechter J, Ludwig AK, Radtke S, et al. Extracellular vesicles improve post-stroke neuroregeneration and prevent postischemic immunosuppression. Stem Cells Transl Med. 2015;4:1131–43.
Dumbrava DA, Surugiu R, Borger V, Ruscu M, Tertel T, Giebel B, et al. Mesenchymal stromal cell-derived small extracellular vesicles promote neurological recovery and brain remodeling after distal middle cerebral artery occlusion in aged rats. Geroscience. 2022;44:293–310.
Gregorius J, Wang C, Stambouli O, Hussner T, Qi Y, Tertel T, et al. Small extracellular vesicles obtained from hypoxic mesenchymal stromal cells have unique characteristics that promote cerebral angiogenesis, brain remodeling and neurological recovery after focal cerebral ischemia in mice. Basic Res Cardiol. 2021;116:40.
Lee JY, Kim E, Choi SM, Kim DW, Kim KP, Lee I, et al. Microvesicles from brain-extract-treated mesenchymal stem cells improve neurological functions in a rat model of ischemic stroke. Sci Rep. 2016;6:33038.
Tuazon JP, Castelli V, Lee JY, Desideri GB, Stuppia L, Cimini AM, et al. Neural stem cells. Adv Exp Med Biol. 2019;1201:79–91.
Moriyama Y, Takagi N, Hashimura K, Itokawa C, Tanonaka K. Intravenous injection of neural progenitor cells facilitates angiogenesis after cerebral ischemia. Brain Behav. 2013;3:43–53.
Dibajnia P, Morshead CM. Role of neural precursor cells in promoting repair following stroke. Acta Pharmacol Sin. 2013;34:78–90.
Wang LP, Pan J, Li Y, Geng J, Liu C, Zhang LY, et al. Oligodendrocyte precursor cell transplantation promotes angiogenesis and remyelination via Wnt/beta-catenin pathway in a mouse model of middle cerebral artery occlusion. J Cereb Blood Flow Metab. 2022;42:757–70.
Savitz SI, Rosenbaum DM, Dinsmore JH, Wechsler LR, Caplan LR. Cell transplantation for stroke. Ann Neurol. 2002;52:266–75.
Zhang P, Li J, Liu Y, Chen X, Lu H, Kang Q, et al. Human embryonic neural stem cell transplantation increases subventricular zone cell proliferation and promotes peri-infarct angiogenesis after focal cerebral ischemia. Neuropathology. 2011;31:384–91.
Chau MJ, Deveau TC, Song M, Gu X, Chen D, Wei L. iPSC Transplantation increases regeneration and functional recovery after ischemic stroke in neonatal rats. Stem Cells. 2014;32:3075–87.
Xia Y, Ling X, Hu G, Zhu Q, Zhang J, Li Q, et al. Small extracellular vesicles secreted by human iPSC-derived MSC enhance angiogenesis through inhibiting STAT3-dependent autophagy in ischemic stroke. Stem Cell Res Ther. 2020;11:313.
Wang J, Yu L, Jiang C, Chen M, Ou C, Wang J. Bone marrow mononuclear cells exert long-term neuroprotection in a rat model of ischemic stroke by promoting arteriogenesis and angiogenesis. Brain Behav Immun. 2013;34:56–66.
Kikuchi-Taura A, Okinaka Y, Takeuchi Y, Ogawa Y, Maeda M, Kataoka Y, et al. Bone marrow mononuclear cells activate angiogenesis via gap junction-mediated cell-cell interaction. Stroke. 2020;51:1279–89.
Pedragosa J, Miro-Mur F, Otxoa-de-Amezaga A, Justicia C, Ruiz-Jaen F, Ponsaerts P, et al. CCR2 deficiency in monocytes impairs angiogenesis and functional recovery after ischemic stroke in mice. J Cereb Blood Flow Metab. 2020;40:S98–S116.
Taguchi A, Soma T, Tanaka H, Kanda T, Nishimura H, Yoshikawa H, et al. Administration of CD34+ cells after stroke enhances neurogenesis via angiogenesis in a mouse model. J Clin Invest. 2004;114:330–8.
Bae CY, Sun HS. TRPM7 in cerebral ischemia and potential target for drug development in stroke. Acta Pharmacol Sin. 2011;32:725–33.
Yang Y, Cai Y, Zhang Y, Liu J, Xu Z. Exosomes secreted by adipose-derived stem cells contribute to angiogenesis of brain microvascular endothelial cells following oxygen-glucose deprivation in vitro through MicroRNA-181b/TRPM7 axis. J Mol Neurosci. 2018;65:74–83.
Molbay M, Ozaydin-Goksu E, Kipmen-Korgun D, Unal A, Ozekinci M, Cebeci E, et al. Human placental trophoblast progenitor cells (hTPCs) promote angiogenesis and neurogenesis after focal cerebral ischemia in rats. Int J Neurosci. 2022;132:258–68.
Liang CC, Shaw SW, Huang YH, Lee TH. Human amniotic fluid stem cells can improve cerebral vascular remodelling and neurological function after focal cerebral ischaemia in diabetic rats. J Cell Mol Med. 2021;25:10185–96.
Kim J, Koo BK, Knoblich JA. Human organoids: model systems for human biology and medicine. Nat Rev Mol Cell Biol. 2020;21:571–84.
Foley KE. Organoids: a better in vitro model. Nat Methods. 2017;14:559–62.
Sato T, Clevers H. SnapShot: growing organoids from stem cells. Cell. 2015;161:1700–e1.
Mansour AA, Goncalves JT, Bloyd CW, Li H, Fernandes S, Quang D, et al. An in vivo model of functional and vascularized human brain organoids. Nat Biotechnol. 2018;36:432–41.
Daviaud N, Friedel RH, Zou H. Vascularization and engraftment of transplanted human cerebral organoids in mouse cortex. eNeuro. 2018;5:ENEURO.0219–18.2018.
Wang Z, Wang SN, Xu TY, Hong C, Cheng MH, Zhu PX, et al. Cerebral organoids transplantation improves neurological motor function in rat brain injury. CNS Neurosci Ther. 2020;26:682–97.
Wang SN, Wang Z, Xu TY, Cheng MH, Li WL, Miao CY. Cerebral organoids repair ischemic stroke brain injury. Transl Stroke Res. 2020;11:983–1000.
Seandel M, Butler J, Lyden D, Rafii S. A catalytic role for proangiogenic marrow-derived cells in tumor neovascularization. Cancer Cell. 2008;13:181–3.
Kokovay E, Li L, Cunningham LA. Angiogenic recruitment of pericytes from bone marrow after stroke. J Cereb Blood Flow Metab. 2006;26:545–55.
Dalkara T, Alarcon-Martinez L, Yemisci M. Pericytes in ischemic stroke. Adv Exp Med Biol. 2019;1147:189–213.
Arimura K, Ago T, Kamouchi M, Nakamura K, Ishitsuka K, Kuroda J, et al. PDGF receptor beta signaling in pericytes following ischemic brain injury. Curr Neurovasc Res. 2012;9:1–9.
Greenberg DA, Jin K. From angiogenesis to neuropathology. Nature. 2005;438:954–9.
Dore-Duffy P, Wang X, Mehedi A, Kreipke CW, Rafols JA. Differential expression of capillary VEGF isoforms following traumatic brain injury. Neurol Res. 2007;29:395–403.
Hoffmann CJ, Harms U, Rex A, Szulzewsky F, Wolf SA, Grittner U, et al. Vascular signal transducer and activator of transcription-3 promotes angiogenesis and neuroplasticity long-term after stroke. Circulation. 2015;131:1772–82.
Ma Y, Wang J, Wang Y, Yang GY. The biphasic function of microglia in ischemic stroke. Prog Neurobiol. 2017;157:247–72.
Jolivel V, Bicker F, Biname F, Ploen R, Keller S, Gollan R, et al. Perivascular microglia promote blood vessel disintegration in the ischemic penumbra. Acta Neuropathol. 2015;129:279–95.
Bisht K, Okojie KA, Sharma K, Lentferink DH, Sun YY, Chen HR, et al. Capillary-associated microglia regulate vascular structure and function through PANX1-P2RY12 coupling in mice. Nat Commun. 2021;12:5289.
Tian Y, Zhu P, Liu S, Jin Z, Li D, Zhao H, et al. IL-4-polarized BV2 microglia cells promote angiogenesis by secreting exosomes. Adv Clin Exp Med. 2019;28:421–30.
Zhang L, Wei W, Ai X, Kilic E, Hermann DM, Venkataramani V, et al. Extracellular vesicles from hypoxia-preconditioned microglia promote angiogenesis and repress apoptosis in stroke mice via the TGF-beta/Smad2/3 pathway. Cell Death Dis. 2021;12:1068.
Ma YZ, Yang SL, He QY, Zhang DH, Chang JL. The role of immune cells in post-stroke angiogenesis and neuronal remodeling: the known and the unknown. Front Immunol. 2021;12:784098.
Ferrara N, Gerber HP, LeCouter J. The biology of VEGF and its receptors. Nat Med. 2003;9:669–76.
Abhinand CS, Raju R, Soumya SJ, Arya PS, Sudhakaran PR. VEGF-A/VEGFR2 signaling network in endothelial cells relevant to angiogenesis. J Cell Commun Signal. 2016;10:347–54.
Carmeliet P, Ferreira V, Breier G, Pollefeyt S, Kieckens L, Gertsenstein M, et al. Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele. Nature. 1996;380:435–9.
Ferrara N, Carver-Moore K, Chen H, Dowd M, Lu L, O’Shea KS, et al. Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene. Nature. 1996;380:439–42.
Cobbs CS, Chen J, Greenberg DA, Graham SH. Vascular endothelial growth factor expression in transient focal cerebral ischemia in the rat. Neurosci Lett. 1998;249:79–82.
Dor Y, Porat R, Keshet E. Vascular endothelial growth factor and vascular adjustments to perturbations in oxygen homeostasis. Am J Physiol Cell Physiol. 2001;280:C1367–74.
Semenza G. Signal transduction to hypoxia-inducible factor 1. Biochem Pharmacol. 2002;64:993–8.
Arany Z, Foo SY, Ma Y, Ruas JL, Bommi-Reddy A, Girnun G, et al. HIF-independent regulation of VEGF and angiogenesis by the transcriptional coactivator PGC-1alpha. Nature. 2008;451:1008–12.
Zhang P, Lei X, Sun Y, Zhang H, Chang L, Li C, et al. Regenerative repair of Pifithrin-alpha in cerebral ischemia via VEGF dependent manner. Sci Rep. 2016;6:26295.
Singh NK, Kundumani-Sridharan V, Rao GN. 12/15-Lipoxygenase gene knockout severely impairs ischemia-induced angiogenesis due to lack of Rac1 farnesylation. Blood. 2011;118:5701–12.
Chen L, Zhu YM, Li YN, Li PY, Wang D, Liu Y, et al. The 15-LO-1/15-HETE system promotes angiogenesis by upregulating VEGF in ischemic brains. Neurol Res. 2017;39:795–802.
Sun Y, Jin K, Xie L, Childs J, Mao XO, Logvinova A, et al. VEGF-induced neuroprotection, neurogenesis, and angiogenesis after focal cerebral ischemia. J Clin Invest. 2003;111:1843–51.
Kusaka N, Sugiu K, Tokunaga K, Katsumata A, Nishida A, Namba K, et al. Enhanced brain angiogenesis in chronic cerebral hypoperfusion after administration of plasmid human vascular endothelial growth factor in combination with indirect vasoreconstructive surgery. J Neurosurg. 2005;103:882–90.
Zechariah A, ElAli A, Doeppner TR, Jin F, Hasan MR, Helfrich I, et al. Vascular endothelial growth factor promotes pericyte coverage of brain capillaries, improves cerebral blood flow during subsequent focal cerebral ischemia, and preserves the metabolic penumbra. Stroke. 2013;44:1690–7.
Zhu Y, Lee C, Shen F, Du R, Young WL, Yang GY. Angiopoietin-2 facilitates vascular endothelial growth factor-induced angiogenesis in the mature mouse brain. Stroke. 2005;36:1533–7.
Ling MF, Quan LL, Lai XM, Lang LM, Li F, Yang XH, et al. VEGFB promotes myoblasts proliferation and differentiation through VEGFR1-PI3K/Akt signaling pathway. Int J Mol Sci. 2021;22:13352.
Huang JB, Hsu SP, Pan HY, Chen SD, Chen SF, Lin TK, et al. Peroxisome proliferator-activated receptor gamma coactivator 1alpha activates vascular endothelial growth factor that protects against neuronal cell death following status epilepticus through PI3K/AKT and MEK/ERK signaling. Int J Mol Sci. 2020;21:7247.
Narasimhan P, Liu J, Song YS, Massengale JL, Chan PH. VEGF Stimulates the ERK 1/2 signaling pathway and apoptosis in cerebral endothelial cells after ischemic conditions. Stroke. 2009;40:1467–73.
Lyons MK, Anderson RE, Meyer FB. Basic fibroblast growth factor promotes in vivo cerebral angiogenesis in chronic forebrain ischemia. Brain Res. 1991;558:315–20.
Zou Y, Hu J, Huang W, Ye S, Han F, Du J, et al. Non-mitogenic fibroblast growth factor 1 enhanced angiogenesis following ischemic stroke by regulating the sphingosine-1-phosphate 1 pathway. Front Pharmacol. 2020;11:59.
Qian RZ, Yue F, Zhang GP, Hou LK, Wang XH, Jin HM. Roles of cyclooxygenase-2 in microvascular endothelial cell proliferation induced by basic fibroblast growth factor. Chin Med J (Engl). 2008;121:2599–603.
Pang Q, Zhang H, Chen Z, Wu Y, Bai M, Liu Y, et al. Role of caveolin-1/vascular endothelial growth factor pathway in basic fibroblast growth factor-induced angiogenesis and neurogenesis after treadmill training following focal cerebral ischemia in rats. Brain Res. 2017;1663:9–19.
Nakamura K, Arimura K, Nishimura A, Tachibana M, Yoshikawa Y, Makihara N, et al. Possible involvement of basic FGF in the upregulation of PDGFRbeta in pericytes after ischemic stroke. Brain Res. 2016;1630:98–108.
Fouda AY, Alhusban A, Ishrat T, Pillai B, Eldahshan W, Waller JL, et al. Brain-derived neurotrophic factor knockdown blocks the angiogenic and protective effects of angiotensin modulation after experimental stroke. Mol Neurobiol. 2017;54:661–70.
Shang J, Deguchi K, Ohta Y, Liu N, Zhang X, Tian F, et al. Strong neurogenesis, angiogenesis, synaptogenesis, and antifibrosis of hepatocyte growth factor in rats brain after transient middle cerebral artery occlusion. J Neurosci Res. 2011;89:86–95.
Gao B, Deng J, Zhang X, Sun H, Jia G, Li J, et al. Effects of mesencephalic astrocyte-derived neurotrophic factor on cerebral angiogenesis in a rat model of cerebral ischemia. Neurosci Lett. 2020;715:134657.
Krupinski J, Issa R, Bujny T, Slevin M, Kumar P, Kumar S, et al. A putative role for platelet-derived growth factor in angiogenesis and neuroprotection after ischemic stroke in humans. Stroke. 1997;28:564–73.
Sugiura S, Kitagawa K, Tanaka S, Todo K, Omura-Matsuoka E, Sasaki T, et al. Adenovirus-mediated gene transfer of heparin-binding epidermal growth factor-like growth factor enhances neurogenesis and angiogenesis after focal cerebral ischemia in rats. Stroke. 2005;36:859–64.
Krupinski J, Vodovotz Y, Li C, Slowik A, Beevers D, Flanders KC, et al. Inducible nitric oxide production and expression of transforming growth factor-beta1 in serum and CSF after cerebral ischaemic stroke in man. Nitric Oxide. 1998;2:442–53.
Krupinski J, Kumar P, Kumar S, Kaluza J. Increased expression of TGF-beta 1 in brain tissue after ischemic stroke in humans. Stroke. 1996;27:852–7.
Ma J, Zhang L, Niu T, Ai C, Jia G, Jin X, et al. Growth differentiation factor 11 improves neurobehavioral recovery and stimulates angiogenesis in rats subjected to cerebral ischemia/reperfusion. Brain Res Bull. 2018;139:38–47.
Zhao HT, Zhang YH, Zhang YH, Shen Y, Zhang YD, Bi FF, et al. NGF/FAK signal pathway is implicated in angiogenesis after acute cerebral ischemia in rats. Neurosci Lett. 2018;672:96–102.
Li XQ, Li FM, Ling L, Li CQ, Zhong YL. Intranasal administration of nerve growth factor promotes angiogenesis via activation of PI3K/Akt signaling following cerebral infarction in rats. Am J Transl Res. 2018;10:3481–92.
Hou Y, Ryu CH, Jun JA, Kim SM, Jeong CH, Jeun SS. IL-8 enhances the angiogenic potential of human bone marrow mesenchymal stem cells by increasing vascular endothelial growth factor. Cell Biol Int. 2014;38:1050–9.
Gertz K, Kronenberg G, Kalin RE, Baldinger T, Werner C, Balkaya M, et al. Essential role of interleukin-6 in post-stroke angiogenesis. Brain. 2012;135:1964–80.
Salmeron K, Aihara T, Redondo-Castro E, Pinteaux E, Bix G. IL-1alpha induces angiogenesis in brain endothelial cells in vitro: implications for brain angiogenesis after acute injury. J Neurochem. 2016;136:573–80.
Huang H, Huang QJ, Wang FX, Milner R, Li LX. Cerebral ischemia-induced angiogenesis is dependent on tumor necrosis factor receptor 1-mediated upregulation of alpha 5 beta 1 and alpha 5 beta 1 integrins. J Neuroinflammation. 2016;13:227.
Wesley UV, Vemuganti R, Ayvaci ER, Dempsey RJ. Galectin-3 enhances angiogenic and migratory potential of microglial cells via modulation of integrin linked kinase signaling. Brain Res. 2013;1496:1–9.
Cheng YH, Jiang YF, Qin C, Shang K, Yuan Y, Wei XJ, et al. Galectin-1 contributes to vascular remodeling and blood flow recovery after cerebral ischemia in mice. Transl Stroke Res. 2022;13:160–70.
Shyu WC, Lin SZ, Yen PS, Su CY, Chen DC, Wang HJ, et al. Stromal cell-derived factor-1 alpha promotes neuroprotection, angiogenesis, and mobilization/homing of bone marrow-derived cells in stroke rats. J Pharmacol Exp Ther. 2008;324:834–49.
Shyu WC, Lin SZ, Yang HI, Tzeng YS, Pang CY, Yen PS, et al. Functional recovery of stroke rats induced by granulocyte colony-stimulating factor-stimulated stem cells. Circulation. 2004;110:1847–54.
Lee ST, Chu K, Jung KH, Ko SY, Kim EH, Sinn DI, et al. Granulocyte colony-stimulating factor enhances angiogenesis after focal cerebral ischemia. Brain Res. 2005;1058:120–8.
Yu X, Peng Y, Liang H, Fu K, Zhao ZH, Xie C, et al. TSLP/TSLPR promote angiogenesis following ischemic stroke via activation of the PI3K/AKT pathway. Mol Med Rep. 2018;17:3411–7.
Ding Q, Liao SJ, Yu J. Axon guidance factor netrin-1 and its receptors regulate angiogenesis after cerebral ischemia. Neurosci Bull. 2014;30:683–91.
Lu HY, Wang YT, He XS, Yuan FL, Lin XJ, Xie BH, et al. Netrin-1 hyperexpression in mouse brain promotes angiogenesis and long-term neurological recovery after transient focal ischemia. Stroke. 2012;43:838–43.
Hoang S, Liauw J, Choi M, Choi M, Guzman RG, Steinberg GK. Netrin-4 enhances angiogenesis and neurologic outcome after cerebral ischemia. J Cereb Blood Flow Metab. 2009;29:385–97.
Yan YP, Lang BT, Vemuganti R, Dempsey RJ. Galectin-3 mediates post-ischemic tissue remodeling. Brain Res. 2009;1288:116–24.
Wesley UV, Sutton IC, Cunningham K, Jaeger JW, Phan AQ, Hatcher JF, et al. Galectin-3 protects against ischemic stroke by promoting neuro-angiogenesis via apoptosis inhibition and Akt/Caspase regulation. J Cereb Blood Flow Metab. 2021;41:857–73.
Li YN, Huang J, He XS, Tang GH, Tang YH, Liu YQ, et al. Postacute stromal cell-derived factor-1 alpha expression promotes neurovascular recovery in ischemic mice. Stroke. 2014;45:1822–9.
Zhang ZG, Zhang L, Croll SD, Chopp M. Angiopoietin-1 reduces cerebral blood vessel leakage and ischemic lesion volume after focal cerebral embolic ischemia in mice. Neuroscience. 2002;113:683–7.
Gridley T. Notch signaling in vascular development and physiology. Development. 2007;134:2709–18.
Fagiani E, Christofori G. Angiopoietins in angiogenesis. Cancer Lett. 2013;328:18–26.
Meng Z, Li M, He Q, Jiang S, Zhang X, Xiao J, et al. Ectopic expression of human angiopoietin-1 promotes functional recovery and neurogenesis after focal cerebral ischemia. Neuroscience. 2014;267:135–46.
Ardelt AA, McCullough LD, Korach KS, Wang MM, Munzenmaier DH, Hurn PD. Estradiol regulates angiopoietin-1 mRNA expression through estrogen receptor-alpha in a rodent experimental stroke model. Stroke. 2005;36:337–41.
Maisonpierre PC, Suri C, Jones PF, Bartunkova S, Wiegand SJ, Radziejewski C, et al. Angiopoietin-2, a natural antagonist for Tie2 that disrupts in vivo angiogenesis. Science. 1997;277:55–60.
Lai DM, Li H, Lee CC, Tzeng YS, Hsieh YH, Hsu WM, et al. Angiopoietin-like protein 1 decreases blood brain barrier damage and edema following focal cerebral ischemia in mice. Neurochem Int. 2008;52:470–7.
Bouleti C, Mathivet T, Coqueran B, Serfaty JM, Lesage M, Berland E, et al. Protective effects of angiopoietin-like 4 on cerebrovascular and functional damages in ischaemic stroke. Eur Heart J. 2013;34:3657–68.
Tang Y, Zhang Y, Zheng M, Chen J, Chen H, Liu N. Effects of treadmill exercise on cerebral angiogenesis and MT1-MMP expression after cerebral ischemia in rats. Brain Behav. 2018;8:e01079.
Hou H, Zhang G, Wang H, Gong H, Wang C, Zhang X. High matrix metalloproteinase-9 expression induces angiogenesis and basement membrane degradation in stroke-prone spontaneously hypertensive rats after cerebral infarction. Neural Regen Res. 2014;9:1154–62.
Yang Y, Thompson JF, Taheri S, Salayandia VM, McAvoy TA, Hill JW, et al. Early inhibition of MMP activity in ischemic rat brain promotes expression of tight junction proteins and angiogenesis during recovery. J Cereb Blood Flow Metab. 2013;33:1104–14.
Ren C, Yao Y, Han R, Huang Q, Li H, Wang B, et al. Cerebral ischemia induces angiogenesis in the peri-infarct regions via Notch1 signaling activation. Exp Neurol. 2018;304:30–40.
Wang P, Guan YF, Li WL, Lu GC, Liu JM, Miao CY. Nicotinamide phosphoribosyltransferase facilitates post-stroke angiogenesis. CNS Neurosci Ther. 2015;21:475–7.
Wang P, Du H, Zhou CC, Song J, Liu X, Cao X, et al. Intracellular NAMPT-NAD+-SIRT1 cascade improves post-ischaemic vascular repair by modulating Notch signalling in endothelial progenitors. Cardiovasc Res. 2014;104:477–88.
Bi JJ, Yi L. Effects of integrins and integrin alphavbeta3 inhibitor on angiogenesis in cerebral ischemic stroke. J Huazhong Univ Sci Technol Med Sci. 2014;34:299–305.
Huang Q, Chen B, Wang F, Huang H, Milner R, Li L. The temporal expression patterns of fibronectin and its receptors-alpha5beta1 and alphavbeta3 integrins on blood vessels after cerebral ischemia. Restor Neurol Neurosci. 2015;33:493–507.
Huang H, Huang Q, Wang F, Milner R, Li L. Cerebral ischemia-induced angiogenesis is dependent on tumor necrosis factor receptor 1-mediated upregulation of alpha5beta1 and alphaVbeta3 integrins. J Neuroinflammation. 2016;13:227.
Chen XM, Chen HS, Xu MJ, Shen JG. Targeting reactive nitrogen species: a promising therapeutic strategy for cerebral ischemia-reperfusion injury. Acta Pharmacol Sin. 2013;34:67–77.
Yingze Y, Zhihong J, Tong J, Yina L, Zhi Z, Xu Z, et al. NOX2-mediated reactive oxygen species are double-edged swords in focal cerebral ischemia in mice. J Neuroinflammation. 2022;19:184.
Matsuda T, Abe T, Wu JL, Fujiki M, Kobayashi H. Hypoxia-inducible factor-1alpha DNA induced angiogenesis in a rat cerebral ischemia model. Neurol Res. 2005;27:503–8.
Miyashita R, Chen L, Oshiro H, Uchino H, Shibasaki F. Int6 silencing causes induction of angiogenic factors in neuronal cells via accumulation of hypoxia-inducible factor 2alpha and decreases brain damage in rats. Neurosci Lett. 2012;528:83–8.
Gu N, Dong Y, Tian Y, Di Z, Liu Z, Chang M, et al. Anti-apoptotic and angiogenic effects of intelectin-1 in rat cerebral ischemia. Brain Res Bull. 2017;130:27–35.
Shi S, Tang M, Li H, Ding H, Lu Y, Gao L, et al. X-box binding protein l splicing attenuates brain microvascular endothelial cell damage induced by oxygen-glucose deprivation through the activation of phosphoinositide 3-kinase/protein kinase B, extracellular signal-regulated kinases, and hypoxia-inducible factor-1alpha/vascular endothelial growth factor signaling pathways. J Cell Physiol. 2019;234:9316–27.
Xue L, Huang J, Zhang T, Wang X, Fu J, Geng Z, et al. PTEN inhibition enhances angiogenesis in an in vitro model of ischemic injury by promoting Akt phosphorylation and subsequent hypoxia inducible factor-1alpha upregulation. Metab Brain Dis. 2018;33:1679–88.
Dong B, Zhang Z, Xie K, Yang Y, Shi Y, Wang C, et al. Hemopexin promotes angiogenesis via up-regulating HO-1 in rats after cerebral ischemia-reperfusion injury. BMC Anesthesiol. 2018;18:2.
Chen X, Zhang X, Chen T, Jiang X, Wang X, Lei H, et al. Inhibition of immunoproteasome promotes angiogenesis via enhancing hypoxia-inducible factor-1alpha abundance in rats following focal cerebral ischaemia. Brain Behav Immun. 2018;73:167–79.
Wang P, Zhao Y, Li Y, Wu J, Yu S, Zhu J, et al. Sestrin2 overexpression attenuates focal cerebral ischemic injury in rat by increasing Nrf2/HO-1 pathway-mediated angiogenesis. Neuroscience. 2019;410:140–9.
Lv MH, Li S, Jiang YJ, Zhang W. The Sphkl/SlP pathway regulates angiogenesis via NOS/NO synthesis following cerebral ischemia-reperfusion. CNS Neurosci Ther. 2020;26:538–48.
Fan G, Li Q, Qian J. C1q contributes to post-stroke angiogenesis via LAIR1-HIF1alpha-VEGF pathway. Front Biosci (Landmark Ed). 2019;24:1050–9.
Li Y, Wu J, Yu S, Zhu J, Zhou Y, Wang P, et al. Sestrin2 promotes angiogenesis to alleviate brain injury by activating Nrf2 through regulating the interaction between p62 and Keap1 following photothrombotic stroke in rats. Brain Res. 2020;1745:146948.
Li Y, Lu Z, Keogh CL, Yu SP, Wei L. Erythropoietin-induced neurovascular protection, angiogenesis, and cerebral blood flow restoration after focal ischemia in mice. J Cereb Blood Flow Metab. 2007;27:1043–54.
Chen GH, Li XL, Deng YQ, Zhou FM, Zou WQ, Jiang WX, et al. The molecular mechanism of EPO regulates the angiogenesis after cerebral ischemia through AMPK-KLF2 signaling pathway. Crit Rev Eukar Gene. 2019;29:105–12.
Bernaudin M, Marti HH, Roussel S, Divoux D, Nouvelot A, MacKenzie ET, et al. A potential role for erythropoietin in focal permanent cerebral ischemia in mice. J Cereb Blood Flow Metab. 1999;19:643–51.
Zhang R, Wang L, Zhang L, Chen J, Zhu Z, Zhang Z, et al. Nitric oxide enhances angiogenesis via the synthesis of vascular endothelial growth factor and cGMP after stroke in the rat. Circ Res. 2003;92:308–13.
Jang H, Oh MY, Kim YJ, Choi IY, Yang HS, Ryu WS, et al. Hydrogen sulfide treatment induces angiogenesis after cerebral ischemia. J Neurosci Res. 2014;92:1520–8.
Hamel D, Sanchez M, Duhamel F, Roy O, Honore JC, Noueihed B, et al. G-protein-coupled receptor 91 and succinate are key contributors in neonatal postcerebral hypoxia-ischemia recovery. Arterioscler Thromb Vasc Biol. 2014;34:285–93.
Chen DD, Wei L, Liu ZR, Yang JJ, Gu XH, Wei ZZ, et al. Pyruvate kinase M2 increases angiogenesis, neurogenesis, and functional recovery mediated by upregulation of stat3 and focal adhesion kinase activities after ischemic stroke in adult mice (vol 15, pg 770, 2018). Neurotherapeutics. 2018;15:836.
Rubanyi GM, Johns A, Kauser K. Effect of estrogen on endothelial function and angiogenesis. Vascul Pharmacol. 2002;38:89–98.
Lu RY, Luo DF, Xiao SH, Yang LH, Zhao J, Ji EN, et al. Kallikrein gene transfer induces angiogenesis and further improves regional cerebral blood flow in the early period after cerebral ischemia/reperfusion in rats. CNS Neurosci Ther. 2012;18:395–9.
Chao J, Chao L. Experimental therapy with tissue kallikrein against cerebral ischemia. Front Biosci. 2006;11:1323–7.
Xia CF, Yin H, Yao YY, Borlongan CV, Chao L, Chao J. Kallikrein protects against ischemic stroke by inhibiting apoptosis and inflammation and promoting angiogenesis and neurogenesis. Hum Gene Ther. 2006;17:206–19.
Tian HL, Chen H, Cui YH, Xu T, Zhou LF. Increased protein and mRNA expression of endostatin in the ischemic brain tissue of rabbits after middle cerebral artery occlusion. Neurosci Bull. 2007;23:35–40.
Avraham Y, Davidi N, Lassri V, Vorobiev L, Kabesa M, Dayan M, et al. Leptin induces neuroprotection neurogenesis and angiogenesis after stroke. Curr Neurovasc Res. 2011;8:313–22.
Meng HM, Song YJ, Zhu JY, Liu Q, Lu PT, Ye N, et al. LRG1 promotes angiogenesis through upregulating the TGF-beta 1 pathway in ischemic rat brain. Mol Med Rep. 2016;14:5535–43.
Fan Y, Zhu W, Yang M, Zhu Y, Shen F, Hao Q, et al. Del-1 gene transfer induces cerebral angiogenesis in mice. Brain Res. 2008;1219:1–7.
Lin TN, Kim GM, Chen JJ, Cheung WM, He YY, Hsu CY. Differential regulation of thrombospondin-1 and thrombospondin-2 after focal cerebral ischemia/reperfusion. Stroke. 2003;34:177–86.
Zan L, Wu H, Jiang J, Zhao S, Song Y, Teng G, et al. Temporal profile of Src, SSeCKS, and angiogenic factors after focal cerebral ischemia: correlations with angiogenesis and cerebral edema. Neurochem Int. 2011;58:872–9.
Shen L, Miao J, Yuan F, Zhao Y, Tang Y, Wang Y, et al. Overexpression of adiponectin promotes focal angiogenesis in the mouse brain following middle cerebral artery occlusion. Gene Ther. 2013;20:93–101.
Leonard MG, Gulati A. Endothelin B receptor agonist, IRL-1620, enhances angiogenesis and neurogenesis following cerebral ischemia in rats. Brain Res. 2013;1528:28–41.
He QW, Xia YP, Chen SC, Wang Y, Huang M, Huang Y, et al. Astrocyte-derived sonic hedgehog contributes to angiogenesis in brain microvascular endothelial cells via RhoA/ROCK pathway after oxygen-glucose deprivation. Mol Neurobiol. 2013;47:976–87.
Huang SS, Cheng H, Tang CM, Nien MW, Huang YS, Lee IH, et al. Anti-oxidative, anti-apoptotic, and pro-angiogenic effects mediate functional improvement by sonic hedgehog against focal cerebral ischemia in rats. Exp Neurol. 2013;247:680–8.
Chen SC, Huang M, He QW, Zhang Y, Opoku EN, Yang H, et al. Administration of Sonic Hedgehog protein induces angiogenesis and Has therapeutic effects after stroke in rats. Neuroscience. 2017;352:285–95.
Yang J, Shi QD, Song TB, Feng GF, Zang WJ, Zong CH, et al. Vasoactive intestinal peptide increases VEGF expression to promote proliferation of brain vascular endothelial cells via the cAMP/PKA pathway after ischemic insult in vitro. Peptides. 2013;42:105–11.
Loh KP, Ng G, Yu CY, Fhu CK, Yu D, Vennekens R, et al. TRPM4 inhibition promotes angiogenesis after ischemic stroke. Pflug Arch. 2014;466:563–76.
Chen CK, Hsu PY, Wang TM, Miao ZF, Lin RT, Juo SHH. TRPV4 activation contributes functional recovery from ischemic stroke via angiogenesis and neurogenesis. Mol Neurobiol. 2018;55:4127–35.
Rodriguez-Grande B, Varghese L, Molina-Holgado F, Rajkovic O, Garlanda C, Denes A, et al. Pentraxin 3 mediates neurogenesis and angiogenesis after cerebral ischaemia. J Neuroinflammation. 2015;12:15.
Ling L, Zhang S, Ji Z, Huang H, Yao G, Wang M, et al. Therapeutic effects of lipo-prostaglandin E1 on angiogenesis and neurogenesis after ischemic stroke in rats. Int J Neurosci. 2016;126:469–77.
Wang Y, Zhang R, Xing X, Guo J, Xie F, Zhang G, et al. Repulsive guidance molecule a suppresses angiogenesis after ischemia/reperfusion injury of middle cerebral artery occlusion in rats. Neurosci Lett. 2018;662:318–23.
Deng G, Qiu Z, Li D, Fang Y, Zhang S. Delayed administration of guanosine improves longterm functional recovery and enhances neurogenesis and angiogenesis in a mouse model of photothrombotic stroke. Mol Med Rep. 2017;15:3999–4004.
Zhou Z, Lu C, Meng S, Dun L, Yin N, An H, et al. Silencing of PTGS2 exerts promoting effects on angiogenesis endothelial progenitor cells in mice with ischemic stroke via repression of the NF-kappaB signaling pathway. J Cell Physiol. 2019;234:23448–60.
Chen Y, Zhang X, He J, Xie Y, Yang Y. Delayed administration of the glucagon-like peptide 1 analog liraglutide promoting angiogenesis after focal cerebral ischemia in mice. J Stroke Cerebrovasc Dis. 2018;27:1318–25.
Xing S, Pan N, Xu W, Zhang J, Li J, Dang C, et al. EphrinB2 activation enhances angiogenesis, reduces amyloid-beta deposits and secondary damage in thalamus at the early stage after cortical infarction in hypertensive rats. J Cereb Blood Flow Metab. 2019;39:1776–89.
Malik AR, Lips J, Gorniak-Walas M, Broekaart DWM, Asaro A, Kuffner MTC, et al. SorCS2 facilitates release of endostatin from astrocytes and controls post-stroke angiogenesis. Glia. 2020;68:1304–16.
Jian R, Yang M, Xu F. Lentiviral-mediated silencing of mast cell-expressed membrane protein 1 promotes angiogenesis of rats with cerebral ischemic stroke. J Cell Biochem. 2019;120:16786–97.
Wang LH, Zhang GL, Liu XY, Peng A, Ren HY, Huang SH, et al. CELSR1 promotes neuroprotection in cerebral ischemic injury mainly through the Wnt/PKC signaling pathway. Int J Mol Sci. 2020;21:1267.
Kim Y, Lee S, Zhang H, Lee S, Kim H, Kim Y, et al. CLEC14A deficiency exacerbates neuronal loss by increasing blood-brain barrier permeability and inflammation. J Neuroinflammation. 2020;17:48.
Huang CY, Dai CF, Gong K, Zuo HC, Chu HL. Apelin-13 protects neurovascular unit against ischemic injuries through the effects of vascular endothelial growth factor. Neuropeptides. 2016;60:67–74.
Wenzel J, Spyropoulos D, Assmann JC, Khan MA, Stolting I, Lembrich B, et al. Endogenous THBD (Thrombomodulin) Mediates Angiogenesis in the Ischemic Brain-Brief Report. Arterioscler Thromb Vasc Biol. 2020;40:2837–44.
Xiao PY, Gu JM, Xu W, Niu XY, Zhang J, Li JJ, et al. RTN4/Nogo-A-S1PR2 negatively regulates angiogenesis and secondary neural repair through enhancing vascular autophagy in the thalamus after cerebral cortical infarction. Autophagy. 2022;18:2711–30.
Chaudhari P, Madaan A, Rivera JC, Charfi I, Habelrih T, Hou X, et al. Neuronal GPR81 regulates developmental brain angiogenesis and promotes brain recovery after a hypoxic ischemic insult. J Cereb Blood Flow Metab. 2022;42:1294–308.
Chen DY, Sun NH, Lu YP, Hong LJ, Cui TT, Wang CK, et al. GPR124 facilitates pericyte polarization and migration by regulating the formation of filopodia during ischemic injury. Theranostics. 2019;9:5937–55.
Fan LS, Chen YC, Liao RJ, Zhao YY, Zhang XN, Chen Z, et al. Antagonism of histamine H3 receptor promotes angiogenesis following focal cerebral ischemia. Acta Pharmacol Sin. 2022;43:2807–16.
Wang C, Jing Q. Non-coding RNAs as biomarkers for acute myocardial infarction. Acta Pharmacol Sin. 2018;39:1110–9.
Yin KJ, Hamblin M, Chen YE. Non-coding RNAs in cerebral endothelial pathophysiology: Emerging roles in stroke. Neurochem Int. 2014;77:9–16.
Heydari E, Alishahi M, Ghaedrahmati F, Winlow W, Khoshnam SE, Anbiyaiee A. The role of non-coding RNAs in neuroprotection and angiogenesis following ischemic stroke. Metab Brain Dis. 2020;35:31–43.
Stępień E, Costa MC, Kurc S, Drożdż A, Cortez-Dias N, Enguita FJ. The circulating non-coding RNA landscape for biomarker research: lessons and prospects from cardiovascular diseases. Acta Pharmacol Sin. 2018;39:1085–99.
Zlokovic BV. Neurovascular mechanisms of Alzheimer’s neurodegeneration. Trends Neurosci. 2005;28:202–8.
Gallego I, Villate-Beitia I, Saenz-del-Burgo L, Puras G, Pedraz JL. Therapeutic opportunities and delivery strategies for brain revascularization in stroke, neurodegeneration, and aging. Pharmacol Rev. 2022;74:439–61.
Biswas S, Cottarelli A, Agalliu D. Neuronal and glial regulation of CNS angiogenesis and barriergenesis. Development. 2020;147:dev182279.
Shah AA, Kamal MA, Akhtar S. Tumor angiogenesis and VEGFR-2: mechanism, pathways and current biological therapeutic interventions. Curr Drug Metab. 2021;22:50–9.
Liu G, Chen T, Ding Z, Wang Y, Wei Y, Wei X. Inhibition of FGF-FGFR and VEGF-VEGFR signalling in cancer treatment. Cell Prolif. 2021;54:e13009.
Wang L, Lin Z, Shao B, Zhuge Q, Jin K. Therapeutic applications of bone marrow-derived stem cells in ischemic stroke. Neurol Res. 2013;35:470–8.
Mello TG, Rosado-de-Castro PH, Campos RMP, Vasques JF, Rangel-Junior WS, Mattos R, et al. Intravenous human umbilical cord-derived mesenchymal stromal cell administration in models of moderate and severe intracerebral hemorrhage. Stem Cells Dev. 2020;29:586–98.
Du SW, Guan J, Mao GS, Liu Y, Ma SH, Bao XJ, et al. Intra-arterial delivery of human bone marrow mesenchymal stem cells is a safe and effective way to treat cerebral ischemia in rats. Cell Transplant. 2014;23:S73–S82.
Chau MJ, Deveau TC, Gu X, Kim YS, Xu Y, Yu SP, et al. Delayed and repeated intranasal delivery of bone marrow stromal cells increases regeneration and functional recovery after ischemic stroke in mice. BMC Neurosci. 2018;19:20.
Jendelova P, Kubinova S, Sandvig I, Erceg S, Sandvig A, Sykova E. Current developments in cell- and biomaterial-based approaches for stroke repair. Expert Opin Biol Ther. 2016;16:43–56.
Erning K, Segura T. Materials to promote recovery after stroke. Curr Opin Biomed Eng. 2020;14:9–17.
Zhong J, Chan A, Morad L, Kornblum HI, Fan G, Carmichael ST. Hydrogel matrix to support stem cell survival after brain transplantation in stroke. Neurorehabil Neural Repair. 2010;24:636–44.
Wang SN, Wang Z, Wang XY, Zhang XP, Xu TY, Miao CY. Humanized cerebral organoids-based ischemic stroke model for discovering of potential anti-stroke agents. Acta Pharmacol Sin. 2022;44:513–23.
Lou YL, Guo F, Liu F, Gao FL, Zhang PQ, Niu X, et al. miR-210 activates notch signaling pathway in angiogenesis induced by cerebral ischemia. Mol Cell Biochem. 2012;370:45–51.
Li LJ, Huang Q, Zhang N, Wang GB, Liu YH. miR-376b-5p regulates angiogenesis in cerebral ischemia. Mol Med Rep. 2014;10:527–35.
Li YA, Mao L, Gao Y, Baral S, Zhou YF, Hu B. MicroRNA-107 contributes to post-stroke angiogenesis by targeting Dicer-1. Sci Rep. 2015;5:13316. https://doi.org/10.1038/srep13316
Feng NP, Wang ZF, Zhang Z, He XJ, Wang CL, Zhang LM. miR-487b promotes human umbilical vein endothelial cell proliferation, migration, invasion and tube formation through regulating THBS1. Neurosci Lett. 2015;591:1–7.
Feng J, Huang T, Huang Q, Chen H, Li Y, He W, et al. Proangiogenic microRNA296 upregulates vascular endothelial growth factor and downregulates Notch1 following cerebral ischemic injury. Mol Med Rep. 2015;12:8141–7.
Meng YC, Ding ZY, Wang HQ, Ning LP, Wang C. Effect of microRNA-155 on angiogenesis after cerebral infarction of rats through AT1R/VEGFR2 pathway. Asian Pac J Trop Med. 2015;8:810–6.
Liu J, Li Q, Zhang KS, Hu B, Niu X, Zhou SM, et al. Downregulation of the long non-coding RNA Meg3 promotes angiogenesis after ischemic brain injury by activating Notch signaling. Mol Neurobiol. 2017;54:8179–90.
Zhan RY, Xu KL, Pan JW, Xu QS, Xu SJ, Shen J. Long noncoding RNA MEG3 mediated angiogenesis after cerebral infarction through regulating p53/NOX4 axis. Biochem Biophys Res Commun. 2017;490:700–6.
Sun J, Tao S, Liu L, Guo D, Xia Z, Huang M. miR1405p regulates angiogenesis following ischemic stroke by targeting VEGFA. Mol Med Rep. 2016;13:4499–505.
He QW, Li Q, Jin HJ, Zhi F, Suraj B, Zhu YY, et al. MiR-150 regulates poststroke cerebral angiogenesis via vascular endothelial growth factor in rats. CNS Neurosci Ther. 2016;22:507–17.
Li Q, He Q, Baral S, Mao L, Li Y, Jin H, et al. MicroRNA-493 regulates angiogenesis in a rat model of ischemic stroke by targeting MIF. FEBS J. 2016;283:1720–33.
Li L, Wang M, Mei Z, Cao W, Yang Y, Wang Y, et al. lncRNAs HIF1A-AS2 facilitates the up-regulation of HIF-1alpha by sponging to miR-153-3p, whereby promoting angiogenesis in HUVECs in hypoxia. Biomed Pharmacother. 2017;96:165–72.
Zhao WJ, Zhang HF, Su JY. Downregulation of microRNA-195 promotes angiogenesis induced by cerebral infarction via targeting VEGFA. Mol Med Rep. 2017;16:5434–40.
Su ZF, Sun ZW, Zhang Y, Wang S, Yu QG, Wu ZB. Regulatory effects of miR-146a/b on the function of endothelial progenitor cells in acute ischemic stroke in mice. Kaohsiung J Med Sci. 2017;33:369–78.
Long FQ, Su QJ, Zhou JX, Wang DS, Li PX, Zeng CS, et al. LncRNA SNHG12 ameliorates brain microvascular endothelial cell injury by targeting miR-199a. Neural Regen Res. 2018;13:1919–26.
Zhao M, Wang J, Xi X, Tan N, Zhang L. SNHG12 promotes angiogenesis following ischemic stroke via regulating miR-150/VEGF pathway. Neuroscience. 2018;390:231–40.
Shan CY, Ma YS. MicroRNA-126/stromal cell-derived factor 1/C-X-C chemokine receptor type 7 signaling pathway promotes post-stroke angiogenesis of endothelial progenitor cell transplantation. Mol Med Rep. 2018;17:5300–5.
Qu M, Pan J, Wang L, Zhou P, Song Y, Wang S, et al. MicroRNA-126 regulates angiogenesis and neurogenesis in a mouse model of focal cerebral ischemia. Mol Ther Nucleic Acids. 2019;16:15–25.
Che FL, Du HS, Zhang WD, Cheng Z, Tong YN. MicroRNA-132 modifies angiogenesis in patients with ischemic cerebrovascular disease by suppressing the NF-kappa B and VEGF pathway. Mol Med Rep. 2018;17:2724–30.
Meng ZY, Kang HL, Duan W, Zheng J, Li QN, Zhou ZJ. MicroRNA-210 Promotes accumulation of neural precursor cells around ischemic foci after cerebral ischemia by regulating the SOCS1-STAT3-VEGF-C pathway. J Am Heart Assoc. 2018;7:e005052.
Fan Y, Ding S, Sun Y, Zhao B, Pan Y, Wan J. MiR-377 regulates inflammation and angiogenesis in rats after cerebral ischemic injury. J Cell Biochem. 2018;119:327–37.
Liu D, Tang ZY, Hu ZJ, Li WW, Yuan WN. MiR-940 regulates angiogenesis after cerebral infarction through VEGF. Eur Rev Med Pharmacol Sci. 2018;22:7899–907.
Liang Z, Chi YJ, Lin GQ, Luo SH, Jiang QY, Chen YK. MiRNA-26a promotes angiogenesis in a rat model of cerebral infarction via PI3K/AKT and MAPK/ERK pathway. Eur Rev Med Pharmacol Sci. 2018;22:3485–92.
Yuan Y, Zhang Z, Wang Z, Liu J. MiRNA-27b regulates angiogenesis by targeting AMPK in mouse ischemic stroke model. Neuroscience. 2019;398:12–22.
Wang ZF, Wang RH, Wang K, Liu XZ. Upregulated long noncoding RNA Snhg1 promotes the angiogenesis of brain microvascular endothelial cells after oxygen-glucose deprivation treatment by targeting miR-199a. Can J Physiol Pharmacol. 2018;96:909–15.
Shi FP, Wang XH, Zhang HX, Shang MM, Liu XX, Sun HM, et al. MiR-103 regulates the angiogenesis of ischemic stroke rats by targeting vascular endothelial growth factor (VEGF). Iran J Basic Med Sci. 2018;21:318–24.
Wang C, Qu Y, Suo R, Zhu Y. Long non-coding RNA MALAT1 regulates angiogenesis following oxygen-glucose deprivation/reoxygenation. J Cell Mol Med. 2019;23:2970–83.
Deng WJ, Fan CH, Shen RL, Wu YZ, Du R, Teng JF. Long noncoding MIAT acting as a ceRNA to sponge microRNA-204-5p to participate in cerebral microvascular endothelial cell injury after cerebral ischemia through regulating HMGB1. J Cell Physiol. 2020;235:4571–86.
Zhou ZW, Zheng LJ, Ren X, Li AP, Zhou WS. LncRNA NEAT1 facilitates survival and angiogenesis in oxygen-glucose deprivation (OGD)-induced brain microvascular endothelial cells (BMECs) via targeting miR-377 and upregulating SIRT1, VEGFA, and BCL-XL. Brain Res. 2019;1707:90–8.
Fan J, Xu W, Nan S, Chang M, Zhang Y. MicroRNA-384-5p promotes endothelial progenitor cell proliferation and angiogenesis in cerebral ischemic stroke through the delta-likeligand 4-mediated notch signaling pathway. Cerebrovasc Dis. 2020;49:39–54.
Wang BX, Xu JJ, Hu J, Hu ML, Huang JM, Zhu XD. Effects of miR-153 on angiogenesis in MCAO rats through Shh signaling pathway. Eur Rev Med Pharmacol Sci. 2019;23:732–9.
Du K, Zhao C, Wang L, Wang Y, Zhang KZ, Shen XY, et al. MiR-191 inhibit angiogenesis after acute ischemic stroke targeting VEZF1. Aging (Albany NY). 2019;11:2762–86.
Wu Z, Liang Y, Yu S. Downregulation of microRNA-103a reduces microvascular endothelial cell injury in a rat model of cerebral ischemia by targeting AXIN2. J Cell Physiol. 2020;235:4720–33.
Deng WJ, Fan CH, Zhao YN, Mao YW, Li JJ, Zhang YG, et al. MicroRNA-130a regulates neurological deficit and angiogenesis in rats with ischaemic stroke by targeting XIAP. J Cell Mol Med. 2020;24:10987–1000.
Sui SH, Sun L, Zhang WJ, Li JM, Han JC, Zheng JP, et al. LncRNA MEG8 attenuates cerebral ischemia after ischemic stroke through targeting miR-130a-5p/VEGFA signaling. Cell Mol Neurobiol. 2021;41:1311–24.
Peng H, Yang H, Xiang X, Li S. MuicroRNA-221 participates in cerebral ischemic stroke by modulating endothelial cell function by regulating the PTEN/PI3K/AKT pathway. Exp Ther Med. 2020;19:443–50.
Sun P, Zhang K, Hassan SH, Zhang X, Tang X, Pu H, et al. Endothelium-targeted deletion of microRNA-15a/16-1 promotes poststroke angiogenesis and improves long-term neurological recovery. Circ Res. 2020;126:1040–57.
Xie K, Cai Y, Yang P, Du F, Wu K. Upregulating microRNA-874-3p inhibits CXCL12 expression to promote angiogenesis and suppress inflammatory response in ischemic stroke. Am J Physiol Cell Physiol. 2020;319:C579–C88.
Li YS, Bi W, Han B, Yuan T, Shi L, Liu Y, et al. MiR-203 Targets to the 3’-UTR of SLUG to suppress cerebral infarction-induced endothelial cell growth and motility. Evid-Based Compl Alt Med. 2021;2021:5597567.
Yu G, Sun W, Wang W, Le C, Liang D, Shuai L. Overexpression of microRNA-202-3p in bone marrow mesenchymal stem cells improves cerebral ischemia-reperfusion injury by promoting angiogenesis and inhibiting inflammation. Aging (Albany NY). 2021;13:11877–88.
Wu Y, Yang S, Zheng Z, Pan H, Jiang Y, Bai X, et al. MiR-191-5p disturbed the angiogenesis in a mice model of cerebral infarction by targeting inhibition of BDNF. Neurol India. 2021;69:1601–7.
Zhou Y, Huang D, Cai Y, Wang M, Ma W, Jiang Z, et al. lncRNA DHFRL1-4 knockdown attenuates cerebral ischemia/reperfusion injury by upregulating the levels of angiogenesis-related genes. Int J Mol Med. 2022;50:108.
Li T, Qing BL, Deng Y, Que XT, Wang CZ, Lu HW, et al. Inhibition of long non-coding RNA zinc finger antisense 1 improves functional recovery and angiogenesis after focal cerebral ischemia via microRNA-144-5p/fibroblast growth factor 7 axis. Bioengineered. 2022;13:1702–16.
Acknowledgements
This work was supported by grants from the National Natural Science Foundation of China Major Project (No. 81730098), the Medical Innovation Major Project (No. 16CXZ009), and the Shanghai Science and Technology Commission Project (No. 21140901000).
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Fang, J., Wang, Z. & Miao, Cy. Angiogenesis after ischemic stroke. Acta Pharmacol Sin 44, 1305–1321 (2023). https://doi.org/10.1038/s41401-023-01061-2
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DOI: https://doi.org/10.1038/s41401-023-01061-2
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