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16 pages, 1891 KiB  
Article
Physicochemical and Functional Characterization of Pear Leathers Enriched with Wild Bilberry and Blackcurrant Pomace Powders
by Ana Maria Blejan, Violeta Nour and Georgiana Gabriela Codină
Agronomy 2024, 14(9), 2048; https://doi.org/10.3390/agronomy14092048 - 7 Sep 2024
Viewed by 282
Abstract
Fruit leathers are convenient, delicious and sophisticated alternatives to natural fruits as a source of nutrients, fibers and bioactive compounds. The present study was conducted to develop new fruit leathers by adding 0.5%, 1.0% and 1.5% wild bilberry (BIPP) and blackcurrant (BCPP) pomace [...] Read more.
Fruit leathers are convenient, delicious and sophisticated alternatives to natural fruits as a source of nutrients, fibers and bioactive compounds. The present study was conducted to develop new fruit leathers by adding 0.5%, 1.0% and 1.5% wild bilberry (BIPP) and blackcurrant (BCPP) pomace powders in pear leather manufactured with honey (5%), pectin (1%) and lemon juice (2.5%) as additional ingredients. The CIEL*a*b* color parameters, titratable acidity, total phenolics content, total anthocyanins content and DPPH radical scavenging activity were determined in the fruit leathers. In addition, the puncturing force, flexibility and adhesiveness of the fruit leathers were measured and sensory analysis was conducted. The results showed that the addition of pomace powders significantly decreased the lightness, chroma and hue angle and increased the titratable acidity of the fruit leathers while a* values decreased in the leathers with BIPP addition. Flexibility slightly decreased while adhesiveness significantly increased with increasing BIPP and BCPP addition level, changes that were perceived as negative in the sensory analysis. The total phenolic content increased by 2.03, 3.26 and 4.45 times at 0.5, 1.0 and 1.5% BIPP addition, respectively, while only by 1.22, 1.42 and 1.60 times at the same levels of BCPP addition. The newly developed fruit leathers could be recommended as alternative snack foods with high nutritional value and functionality. Full article
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Figure 1
<p>Drying curves at 57 °C of the control pear leather and fruit leathers made with addition of (<b>a</b>) bilberry pomace powder; (<b>b</b>) blackcurrant pomace powder.</p>
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<p>The appearance of the fruit leathers.</p>
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<p>Sensory profile of control pear leather and pear leathers enriched with (<b>a</b>) bilberry pomace powder; (<b>b</b>) blackcurrant pomace powder.</p>
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<p>Sensory profile of control pear leather and pear leathers enriched with (<b>a</b>) bilberry pomace powder; (<b>b</b>) blackcurrant pomace powder.</p>
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10 pages, 538 KiB  
Article
Impact of Hepatitis Delta Virus Infection on the Selection of Hepatitis B Surface Antigen Mutations
by Kabo Baruti, Wonderful T. Choga, Bonolo B. Phinius, Basetsana Phakedi, Lynnette Bhebhe, Gorata G. A. Mpebe, Patience C. Motshosi, Tsholofelo Ratsoma, Sikhulile Moyo, Mosimanegape Jongman, Motswedi Anderson and Simani Gaseitsiwe
Genes 2024, 15(8), 982; https://doi.org/10.3390/genes15080982 - 25 Jul 2024
Viewed by 558
Abstract
The interaction of multiple viruses in one host is thought to enhance the development of mutations. However, the impact of hepatitis D virus (HDV) positivity on the development of unique hepatitis B virus (HBV) mutations among people living with human immunodeficiency virus (HIV) [...] Read more.
The interaction of multiple viruses in one host is thought to enhance the development of mutations. However, the impact of hepatitis D virus (HDV) positivity on the development of unique hepatitis B virus (HBV) mutations among people living with human immunodeficiency virus (HIV) (PLWH) remains poorly understood in African countries, including Botswana. We used HBV sequences generated from the Botswana Combination Prevention Project (BCPP), which is the largest pair-matched cluster-randomized HIV trial in Botswana. Only participants with available HBV sequences (n = 55) were included in our study ([HIV/HBV-positive (n = 50) and HIV/HBV/HDV-positive (n = 5)]. Geno2pheno was used to determine HBV genotypes, and HBV surface region sequences (all subgenotype A1) were aligned in AliView for mutational analysis, while the impact of mutations was assessed using Phyre2. Our results identified 182 common mutations between the two groups. In the HIV/HBV/HDV cohort, only three mutations (L95W, W156Q, C221Y) were classified as deleterious, with only L95W being the most frequent. In the HIV/HBV cohort, four mutations (W199R, C221A, C221S, W223G) were also classified as deleterious. Our results demonstrate the presence of unique HBV mutations among the HIV/HBV/HDV-positive cohort. Functional characterization of these mutations is recommended to determine their effect on HDV. Full article
(This article belongs to the Special Issue Molecular Epidemiology, Genome and Evolution of Viruses)
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<p>Summary flow chart of samples tested in the study.</p>
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18 pages, 2340 KiB  
Article
Hepatitis B Virus Prevalence among HIV-Uninfected People Living in Rural and Peri-Urban Areas in Botswana
by Motswedi Anderson, Thabo Mangogola, Bonolo B. Phinius, Gorata Mpebe, Christopher O. Aimakhu, Wonderful T. Choga, Basetsana Phakedi, Lynnette N. Bhebhe, Doreen Ditshwanelo, Kabo Baruti, Linda Mpofu-Dobo, Lebogang Othusitse, Tsholofelo Ratsoma, Tendani Gaolathe, Joseph Makhema, Roger Shapiro, Shahin Lockman, Sikhulile Moyo and Simani Gaseitsiwe
Microorganisms 2024, 12(6), 1207; https://doi.org/10.3390/microorganisms12061207 - 15 Jun 2024
Viewed by 1151
Abstract
(1) Background: we determined the prevalence of the hepatitis B virus (HBV) amongst people without human immunodeficiency virus (HIV) in rural and peri-urban areas in Botswana. (2) Methods: We screened for the hepatitis B surface antigen (HBsAg) from archived plasma samples of people [...] Read more.
(1) Background: we determined the prevalence of the hepatitis B virus (HBV) amongst people without human immunodeficiency virus (HIV) in rural and peri-urban areas in Botswana. (2) Methods: We screened for the hepatitis B surface antigen (HBsAg) from archived plasma samples of people without HIV (n = 2135) randomly selected from the Botswana Combination Prevention Program (BCPP) (2013–2018). We sequenced 415 bp of the surface region using BigDye sequencing chemistry. (3) Results: The median age of participants was 31 (IQR: 24–46) and 64% (1360/2135) were female. HBV prevalence was 4.0% (86/2135) [95% CI: 3.3–4.9]) and ranged between 0–9.2%. Older participants (>35 years) had increased odds of HBV positivity (OR: 1.94; 95% CI: [1.32–2.86]; p = 0.001). Thirteen samples were sequenced and seven (53.8%) were genotype A, three (23.1%) were genotype D and genotype E each. Clinically significant mutations were identified in the surface region, but no classic drug resistance mutations were identified. (4) Conclusions: We report an HBV prevalence of 4.0% (95% CI 3.3–4.9) among people without HIV in rural and peri-urban communities in Botswana with varying rates in different communities. A comprehensive national HBV program is required in Botswana to guide HBV prevention, testing and management. Full article
(This article belongs to the Special Issue Control and Elimination of Viral Hepatitis)
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<p>HBV prevalence by community among people without HIV from the BCPP cohort.</p>
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<p>(<b>A</b>) Age by community, (<b>B</b>) Heat map showing differences in age distribution between communities, (<b>C</b>) Boxplots showing the age distribution across the BCPP communities with both HBV negative (green) and positive (orange) cases. Pairwise comparison was conducted by age between communities and between HBV negative and positive cases using Wilcoxon test. The significance levels of ns, *, **, and *** represent <span class="html-italic">p</span>-values &gt; 0.05, &lt;0.05, &lt;0.01 and &lt;0.001, respectively.</p>
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<p>(<b>A</b>) Age by community, (<b>B</b>) Heat map showing differences in age distribution between communities, (<b>C</b>) Boxplots showing the age distribution across the BCPP communities with both HBV negative (green) and positive (orange) cases. Pairwise comparison was conducted by age between communities and between HBV negative and positive cases using Wilcoxon test. The significance levels of ns, *, **, and *** represent <span class="html-italic">p</span>-values &gt; 0.05, &lt;0.05, &lt;0.01 and &lt;0.001, respectively.</p>
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<p>Phylogenetic analysis of HBV strains obtained from HIV-uninfected participants living in rural and peri-urban areas in Botswana. A phylogenetic analysis of a 415 bp fragment of the HBV from different isolates with seven HBV A, three HBV D and three HBV E sequences clustered with the matching HBV genotype Botswana reference. Study sequences are denoted by the name HBV followed by a number and the references begin with an accession number followed by a letter denoting the genotype. Genotype A is coloured red, D is coloured blue and E is coloured green. Black is genotype G which was used for rooting.</p>
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<p>(<b>A</b>) Frequency of surface region mutations, (<b>B</b>) Frequency of rt region mutations. *: stop codon.</p>
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<p>(<b>A</b>) Frequency of surface region mutations, (<b>B</b>) Frequency of rt region mutations. *: stop codon.</p>
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17 pages, 4326 KiB  
Article
Electromagnetic Detection System with Magnetic Dipole Source for Near-Surface Detection
by Xian Liao, Zhengyu Xu, Wei Liu, Heng-Ming Tai, Jie Zhou, Xiao Ma and Zhihong Fu
Sensors 2023, 23(24), 9771; https://doi.org/10.3390/s23249771 - 12 Dec 2023
Cited by 1 | Viewed by 1094
Abstract
This paper proposes a nondestructive, separate transmitter-receiver (TX-RX) electromagnetic measurement system for near-surface detection. Different from the traditional dual-coil integrated design, the proposed transient electromagnetic (TEM) system performs shallow subsurface detection using independent TX coil and movable RX coils. This configuration requires a [...] Read more.
This paper proposes a nondestructive, separate transmitter-receiver (TX-RX) electromagnetic measurement system for near-surface detection. Different from the traditional dual-coil integrated design, the proposed transient electromagnetic (TEM) system performs shallow subsurface detection using independent TX coil and movable RX coils. This configuration requires a large primary field so that the far-away secondary field is able to generate reliably induced voltages. To achieve this goal, a bipolar current-pulsed power supply (BCPPS) with a late resonant charging strategy is designed to produce a sufficiently large magnetic moment for the exciting coil with low source interference. The magnetic dipole source (MDS) with a large proportion of weight is separated from the field observation device and does not need to be dragged or transported during the detection process. This setup lowers the weight of the scanning device to 3 kg and greatly improves the measurement efficiency. The results of the laboratory test verify the effectiveness of the separate MDS and RX module system. Field experimental detection further demonstrates that the proposed system can realize highly efficient and shallow surface detection within a 200 m range of the MDS device. Full article
(This article belongs to the Special Issue Advanced Sensing and Control Technologies in Power Electronics)
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Figure 1
<p>Schematics of the different TEM detection systems: (<b>a</b>) traditional TX-RX-integrated detection system; (<b>b</b>) proposed detection system with magnetic dipole source.</p>
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<p>Magnetic field components in a dipole field coordinate system for a typical vertical MDS.</p>
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<p>Geoelectric model and finite element simulation results of MDS detection when <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>t</mi> </mrow> <mrow> <mi>s</mi> </mrow> </msub> <mo>=</mo> <mn>200</mn> <mtext> </mtext> <mi mathvariant="sans-serif">μ</mi> <mi mathvariant="normal">s</mi> </mrow> </semantics></math>: (<b>a</b>) Three-dimensional geoelectric model and simulation parameters. (<b>b</b>) Field distribution Hz (A/m) with <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>I</mi> </mrow> <mrow> <mi>p</mi> </mrow> </msub> <mo>=</mo> <mn>20</mn> <mtext> </mtext> <mi mathvariant="normal">A</mi> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>t</mi> </mrow> <mrow> <mi>f</mi> </mrow> </msub> <mo>=</mo> <mn>200</mn> <mtext> </mtext> <mi mathvariant="sans-serif">μ</mi> <mi mathvariant="normal">s</mi> </mrow> </semantics></math>. (<b>c</b>) Field distribution Hz (A/m) with <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>I</mi> </mrow> <mrow> <mi>p</mi> </mrow> </msub> <mo>=</mo> <mn>300</mn> <mtext> </mtext> <mi mathvariant="normal">A</mi> </mrow> </semantics></math> and <math display="inline"><semantics> <mrow> <msub> <mrow> <mi>t</mi> </mrow> <mrow> <mi>f</mi> </mrow> </msub> <mo>=</mo> <mn>400</mn> <mtext> </mtext> <mi mathvariant="sans-serif">μ</mi> <mi mathvariant="normal">s</mi> </mrow> </semantics></math>.</p>
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<p>Conventional BCPPS for ground TEM detection: (<b>a</b>) Clamping topology with TVS. (<b>b</b>) Steep pulse current source with boost topology.</p>
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<p>Proposed BCPPS for MDS in the ground TEM detection.</p>
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<p>Waveforms of critical elements for the steady state operation of the proposed BCPPS circuit in <a href="#sensors-23-09771-f005" class="html-fig">Figure 5</a>. Red shade: data measuring window. Blue shade: capacitor <span class="html-italic">C<sub>b</sub></span> charging window.</p>
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<p>Four operation topologies of the proposed BCPPS, indicated by the red loops: (<b>a</b>) Mode 1. (<b>b</b>) Mode 2. (<b>c</b>) Mode 3. (<b>d</b>) Mode 4.</p>
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<p>Equivalent circuit of the resonant charging loop.</p>
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<p>Composition of the proposed electromagnetic measurement system with separated MDS: (<b>a</b>) Functional block diagram of the system. (<b>b</b>) Physical photos of the system.</p>
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<p>RX signal acquisition and preliminary processing.</p>
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<p>Current pulse waveforms generated using various BCPPS circuits: (<b>a</b>) Clamping scheme with TVS. (<b>b</b>) Steep pulse current source with boost module. (<b>c</b>) Proposed topology for MDS with different converter gains.</p>
Full article ">Figure 12
<p>Measured induced voltages of the survey line. The measuring points are located at the intersection of the dotted lines: (<b>a</b>) Experimental layout of the detection process. (<b>b</b>) Z-coil data during the early turn-off process at measuring points. (<b>c</b>) The simulation results for induced voltage in scenarios with and without a metal body.</p>
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<p>Position imaging of the induced voltage scanning.</p>
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10 pages, 1170 KiB  
Article
Clinical Assessment of Biphasic Calcium Phosphate in Granules and Paste Forms in Human Maxillary Sinus Bone Augmentation: A Randomized, Split-Mouth Clinical Trial
by João Paulo Bonardi, Rodrigo dos Santos Pereira, Carlos F. Mourão, Bruno Coelho Mendes, Adam Lowenstein, Pietro Montemezzi, Flavio Giubilato, Roberta Okamoto and Eduardo Hochuli-Vieira
Materials 2023, 16(3), 1059; https://doi.org/10.3390/ma16031059 - 25 Jan 2023
Cited by 2 | Viewed by 1231
Abstract
The aim of the present study is to compare the biphasic calcium phosphate (BCP) using two different forms—(1) granules and (2) paste—in human maxillary sinus bone reconstruction as a split-mouth study using histomorphometric and immunolabeling for osteocalcin. Ten patients with bilateral maxillary posterior [...] Read more.
The aim of the present study is to compare the biphasic calcium phosphate (BCP) using two different forms—(1) granules and (2) paste—in human maxillary sinus bone reconstruction as a split-mouth study using histomorphometric and immunolabeling for osteocalcin. Ten patients with bilateral maxillary posterior partial edentulism were selected in order to reconstruct bone height. They were divided into two groups: BCPG and BCP-P. After six months of bone healing, biopsies were harvested to assess the new bone formation and immunostaining for osteocalcin. The BCP g group had the following results: mean of bone formation in pristine bone 49.4 ± 21.6%, intermediate 49.4 ± 16.2%, and apical 55.3 ± 21.4%. The group BCP-P had a mean of 41.9 ± 17.3% in the pristine bone region, 37.5 ± 7.8% for intermediate, and 39.0 ± 13.5% for apical. The osteocalcin immunolabeling was high for both groups, demonstrating bone calcification. Thus, the two biomaterials present suitable results for the placement of dental implants. Full article
(This article belongs to the Special Issue Advanced Dental Materials for Periodontal and Bone Regeneration)
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<p>Study flow diagram.</p>
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<p>Image showing histological sections for BCP-G (<b>A</b>) and BCP-P (<b>B</b>). Immunolabeling for osteocalcin for BCP-G (<b>C</b>) and BCP-P (<b>D</b>). (<b>•</b>) Biomaterial remaining; (▲) Immunostaining for osteocalcin on bone surface. [Magnification, ×12.5 for <b>A</b>,<b>B</b>; ×40 for <b>C</b>,<b>D</b>].</p>
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<p>Graph showing the histomorphometric results of new bone formed in each region evaluated for BCP-G and BCP-P after six months of bone repair in human maxillary sinus augmentation.</p>
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<p>Graph showing the histomorphometric results of connective tissue in each region evaluated for BCP-G and BCP-P after six months of bone repair in human maxillary sinus augmentation.</p>
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15 pages, 1149 KiB  
Article
Barriers and Enablers to Buying Biodegradable and Compostable Plastic Packaging
by Ayşe Lisa Allison, Fabiana Lorencatto, Susan Michie and Mark Miodownik
Sustainability 2021, 13(3), 1463; https://doi.org/10.3390/su13031463 - 30 Jan 2021
Cited by 32 | Viewed by 11006
Abstract
Biodegradable and compostable plastic packaging (BCPP) has the potential to reduce a global plastic waste problem. We aimed to identify influences on buying BCPP as a basis for designing strategies that enable BCPP’s environmental benefits. Using a UK-focused citizen science dataset, we thematically [...] Read more.
Biodegradable and compostable plastic packaging (BCPP) has the potential to reduce a global plastic waste problem. We aimed to identify influences on buying BCPP as a basis for designing strategies that enable BCPP’s environmental benefits. Using a UK-focused citizen science dataset, we thematically analysed 610 survey responses to a question exploring reasons for BCPP purchase. Themes are categorised as barriers and enablers and according to the components of the Capability, Opportunity, Motivation, and Behaviour (COM-B) model of behaviour. Key barriers concerned: psychological capability (not understanding terminology used to label packaging, not taking notice of packaging, and preferring other types of packaging and product qualities); reflective motivation (negative beliefs about BCPP’s environmental impacts and skepticism over decomposition claims), and physical opportunity (no access to appropriate waste management). Key enablers concern: reflective motivation (positive beliefs about BCPP’s environmental impact and resolve to behave pro-environmentally) and physical opportunity (access to appropriate waste management). Reducing ambiguity concerning the labels of biodegradable and compostable may reduce skepticism over environmental claims of packaging. Interventions should improve information about the source of the packaging material, how the packaging waste is processed, and how to dispose of the packaging. This will not be sufficient unless facilities for local BCPP waste collection and processing are increased. Full article
(This article belongs to the Section Psychology of Sustainability and Sustainable Development)
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<p>The COM-B model—a framework for understanding behaviour.</p>
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<p>The steps undertaken to create the thematic analysis.</p>
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14 pages, 1114 KiB  
Article
The Impact of Small Extracellular Vesicles on Lymphoblast Trafficking across the Blood-Cerebrospinal Fluid Barrier In Vitro
by Ulrike Erb, Julia Hikel, Svenja Meyer, Hiroshi Ishikawa, Thomas S. Worst, Katja Nitschke, Philipp Nuhn, Stefan Porubsky, Christel Weiss, Horst Schroten, Rüdiger Adam and Michael Karremann
Int. J. Mol. Sci. 2020, 21(15), 5491; https://doi.org/10.3390/ijms21155491 - 31 Jul 2020
Cited by 7 | Viewed by 3069
Abstract
Central nervous System (CNS) disease in pediatric acute lymphoblastic leukemia (ALL) is a major concern, but still, cellular mechanisms of CNS infiltration are elusive. The choroid plexus (CP) is a potential entry site, and, to some extent, invasion resembles CNS homing of lymphocytes [...] Read more.
Central nervous System (CNS) disease in pediatric acute lymphoblastic leukemia (ALL) is a major concern, but still, cellular mechanisms of CNS infiltration are elusive. The choroid plexus (CP) is a potential entry site, and, to some extent, invasion resembles CNS homing of lymphocytes during healthy state. Given exosomes may precondition target tissue, the present work aims to investigate if leukemia-derived exosomes contribute to a permissive phenotype of the blood-cerebrospinal fluid barrier (BCSFB). Leukemia-derived exosomes were isolated by ultracentrifugation from the cell lines SD-1, Nalm-6, and P12-Ichikawa (P12). Adhesion and uptake to CP epithelial cells and the significance on subsequent ALL transmigration across the barrier was studied in a human BCSFB in vitro model based on the HiBCPP cell line. The various cell lines markedly differed regarding exosome uptake to HiBCPP and biological significance. SD-1-derived exosomes associated to target cells unspecifically without detectable cellular effects. Whereas Nalm-6 and P12-derived exosomes incorporated by dynamin-dependent endocytosis, uptake in the latter could be diminished by integrin blocking. In addition, only P12-derived exosomes led to facilitated transmigration of the parental leukemia cells. In conclusion, we provide evidence that, to a varying extent, leukemia-derived exosomes may facilitate CNS invasion of ALL across the BCSFB without destruction of the barrier integrity. Full article
(This article belongs to the Special Issue Choroid Plexus: Novel Functions for an Old Structure)
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<p>Time- and dose-dependent uptake/binding of acute lymphoblastic leukemia (ALL) cell-derived exosomes to blood-cerebrospinal fluid barrier (BCSFB) in vitro model. Fluorescently labeled exosomes were added onto the basolateral side of HiBCPP cells grown in inverted culture as indicated and uptaken/bound exosomes were quantified by fluorescent microscopy. Relative fluorescence intensity (RFI) was measured in 15 fields of view (20× objective). (<b>A</b>) Representative observation field of untreated control HiBCPP cells and HiBCPP cells incubated with DiIC18(3) labeled exosomes (red) (16 μg, 48 h). HiBCPP cells were visualized by nuclei staining (DAPI, blue). (<b>B</b>) Time-dependent uptake/binding of ALL-derived exosomes (16 μg per filter; SD-1, Nalm-6, and P12, respectively) for indicated time points from basolateral side, and (<b>C</b>) dose-dependent uptake/binding of ALL-derived exosomes (48 h; SD-1, Nalm-6, and P12, respectively) for indicated amounts per filter from basolateral side. (<b>D</b>) Barrier integrity following exosome incubation was determined by transepithelial electrical resistance (TEER) and showed no significant alterations compared to untreated control. All data shown are box plots with whiskers of at least 3 independent experiments performed in triplicates. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Mechanism of uptake/binding of acute lymphoblastic leukemia (ALL) cell-derived exosomes to blood-cerebrospinal fluid barrier (BCSFB) in vitro model. DiIC18(3) labeled exosomes (16 µg per filter) were added onto the basolateral side of HiBCPP cells grown in inverted culture and incubated for 48 h. The nuclei were stained with DAPI solution. Relative fluorescence intensity (RFI) of exosomes was quantified by fluorescent microscopy (15 fields of view, 20× objective). (<b>A</b>) Fluorescently labeled exosomes were pretreated with 4 µg/mL anti-integrin-antibody (anti-ITGα5; anti-ITGαV; anti-ITGβ1; anti-ITGβ3) for 30 min at 37 °C before incubation on HiBCPP cells. (<b>B</b>) HiBCPP cells were pretreated with chemical inhibitors (10 µg/mL heparin; 5 μg/mL cytochalasin D; 50 µM chlorpromazine; 80 µM dynasore) for 1 h at 37 °C before incubation. HiBCPP cells were washed with acidic PBS (pH = 2.5) after incubation to strip off adherend exosomes. Data shown are box plots with whiskers of at least 3 independent experiments performed in triplicates. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Exosomal pre-incubation enhances transmigration across blood-cerebrospinal fluid barrier (BCSFB) in vitro model of T-ALL cell line P12 but not of B-cell precursor (BCP)-ALL cell lines in time-dependent manner. CellTracker™ Green labeled ALL cells were added for 6 h onto the basolateral side of untreated HiBCPP cells or HiBCPP cells pre-incubated with 16 μg unlabeled exosomes for indicated time-points. C-X-C motif chemokine ligand 12 (CXCL12) (100 ng/mL) was used as chemoattractant. Migrated ALL cells (SD-1, Nalm-6, and P12, respectively) were quantified in the lower compartment by fluorescent microscopy (10 fields of view, 10× objective). Data shown are box plots with whiskers of at least 3 independent experiments performed in triplicates. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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11 pages, 322 KiB  
Perspective
An Expanded Agenda for the Primary Prevention of Breast Cancer: Charting a Course for the Future
by Mary C. White, Marion (Mhel) H. E. Kavanaugh-Lynch, Shauntay Davis-Patterson and Nancy Buermeyer
Int. J. Environ. Res. Public Health 2020, 17(3), 714; https://doi.org/10.3390/ijerph17030714 - 22 Jan 2020
Cited by 9 | Viewed by 6377
Abstract
Advances in breast cancer science, early detection, and treatment have resulted in improvements in breast cancer survival but not in breast cancer incidence. After skin cancer, breast cancer is the most common cancer diagnosis in the United States. Each year, nearly a quarter [...] Read more.
Advances in breast cancer science, early detection, and treatment have resulted in improvements in breast cancer survival but not in breast cancer incidence. After skin cancer, breast cancer is the most common cancer diagnosis in the United States. Each year, nearly a quarter million U.S. women receive a breast cancer diagnosis, and the number continues to rise each year with the growth in the population of older women. Although much remains to be understood about breast cancer origins and prevention, action can be taken on the existing scientific knowledge to address the systemic factors that drive breast cancer risk at the population level. The California Breast Cancer Research Program funded a team at Breast Cancer Prevention Partners (BCPP) to convene leaders in advocacy, policy, and research related to breast cancer prevention from across the state of California. The objective was the development of a strategic plan to direct collective efforts toward specific and measurable objectives to reduce the incidence of breast cancer. The structured, innovative approach used by BCPP to integrate scientific evidence with community perspectives provides a model for other states to consider, to potentially change the future trajectory of breast cancer incidence in the United States. Full article
(This article belongs to the Special Issue Advancing Primary Prevention of Breast Cancer)
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