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Search Results (37,769)

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22 pages, 2393 KiB  
Article
SmartISM 2.0: A Roadmap and System to Implement Fuzzy ISM and Fuzzy MICMAC
by Naim Ahmad
Sustainability 2024, 16(20), 8873; https://doi.org/10.3390/su16208873 (registering DOI) - 13 Oct 2024
Abstract
Interpretive structural modeling (ISM) is a widely used technique to establish hierarchical relationships among a set of variables in diverse domains, including sustainability. This technique is generally coupled with MICMAC (Matrice d’Impacts Croisés Multiplication Appliquée á un Classement (cross-impact matrix multiplication applied to [...] Read more.
Interpretive structural modeling (ISM) is a widely used technique to establish hierarchical relationships among a set of variables in diverse domains, including sustainability. This technique is generally coupled with MICMAC (Matrice d’Impacts Croisés Multiplication Appliquée á un Classement (cross-impact matrix multiplication applied to classification)) to classify variables in four clusters, although the manual application of the technique is complex and prone to error. In one of the previous works, a novel concept of reduced conical matrix was introduced, and the SmartISM software was developed for the user-friendly implementation of ISM and MICMAC. The web-based SmartISM software has been used more than 48,123 times in 87 countries to generate ISM models and MICMAC diagrams. This work attempts to identify existing approaches to fuzzy ISM and fuzzy MICMAC and upscale the SmartISM to incorporate fuzzy approaches. The fuzzy set theory proposed by Zadeh 1965 and Goguen 1969 helps the decision makers to provide their input with the consideration of vagueness in the real environment. The systematic review of 32 studies identified five significant approaches that have used different linguistic scales, fuzzy numbers, and defuzzification methods. Further, the approaches have differences in either using single or double defuzzification, and the aggregation of inputs of decision makers either before or after defuzzification, as well as the incorporation of transitivity either before or after defuzzification. A roadmap was devised to aggregate and generalize different approaches. Further, two of the identified approaches have been implemented in SmartISM 2.0 and the results have been reported. Finally, the comparative analysis of different approaches using SmartISM 2.0 in the area of digital transformation shows that, with a wide flexibility of fuzzy scales, the results converge and improve the confidence in the final model. The roadmap and SmartISM 2.0 will help in the implementation of fuzzy ISM and fuzzy MICMAC in a more robust and informed way. Full article
29 pages, 1713 KiB  
Article
Optimized Trajectory Tracking for ROVs Using DNN + ENMPC Strategy
by Guanghao Yang, Weidong Liu, Le Li, Jingming Xu, Liwei Guo and Kang Zhang
J. Mar. Sci. Eng. 2024, 12(10), 1827; https://doi.org/10.3390/jmse12101827 (registering DOI) - 13 Oct 2024
Abstract
This study introduces an innovative double closed-loop 3D trajectory tracking approach, integrating deep neural networks (DNN) with event-triggered nonlinear model predictive control (ENMPC), specifically designed for remotely operated vehicles (ROVs) under external disturbance conditions. In contrast to single-loop model predictive control, the proposed [...] Read more.
This study introduces an innovative double closed-loop 3D trajectory tracking approach, integrating deep neural networks (DNN) with event-triggered nonlinear model predictive control (ENMPC), specifically designed for remotely operated vehicles (ROVs) under external disturbance conditions. In contrast to single-loop model predictive control, the proposed double closed-loop control system operates in two distinct phases: (1) The outer loop controller uses a DNN controller to replace the LMPC controller, overcoming the uncertainties in the kinematic model while reducing the computational burden. (2) The inner loop velocity controller is designed using a nonlinear model predictive control (NMPC) algorithm with its closed-loop stability proven. A DNN + ENMPC 3D trajectory tracking method is proposed, integrating a velocity threshold-triggered mechanism into the inner-loop NMPC controller to reduce computational iterations while sacrificing only a small amount of tracking control performance. Finally, simulation results indicate that compared with the ENMPC algorithm, NMPC + ENMPC can better track the desired trajectory, reduce thruster oscillations, and further minimize the computational load. Full article
(This article belongs to the Special Issue Intelligent Measurement and Control System of Marine Robots)
15 pages, 8087 KiB  
Article
A Novel Caterpillar-Inspired Vascular Interventional Robot Navigated by Magnetic Sinusoidal Mechanism
by Xinping Zhu, Hanwei Zhou, Xiaoxiao Zhu and Kundong Wang
Actuators 2024, 13(10), 412; https://doi.org/10.3390/act13100412 (registering DOI) - 13 Oct 2024
Abstract
Magnetic soft continuum robots (MSCRs) hold significant potential in fulfilling the requirements of vascular interventional robots, enabling safe access to difficult-to-reach areas with enhanced active maneuverability, shape morphing capabilities, and stiffness variability. Their primary advantage lies in their tether-less actuation mechanism that can [...] Read more.
Magnetic soft continuum robots (MSCRs) hold significant potential in fulfilling the requirements of vascular interventional robots, enabling safe access to difficult-to-reach areas with enhanced active maneuverability, shape morphing capabilities, and stiffness variability. Their primary advantage lies in their tether-less actuation mechanism that can safely adapt to complex vessel structures. Existing commercial MSCRs primarily employ a magnetic-pull strategy, which suffers from insufficient driving force and a single actuation strategy, limiting their clinical applicability. Inspired by the inchworm crawling locomotion gait, we herein present a novel MSCR that integrates a magnetic sinusoidal actuation mechanism with adjustable frequency and kirigami structures. The developed MSCRs consist of two permanent magnets connected by a micro-spring, which is coated with a silicone membrane featuring a specific notch array. This design enables bio-inspired crawling with controllable velocity and active maneuverability. An analytical model of the magnetic torque and finite element analysis (FEA) simulations of the MSCRs has been constructed. Additionally, the prototype has been validated through two-dimensional in-vitro tracking experiments with actuation frequencies ranging from 1 to 10 Hz. Its stride efficiency has also been verified in a three-dimensional (3D) coronary artery phantom. Diametrically magnetized spherical chain tip enhances active steerability. Kirigami skin is coated over the novel guidewire and catheter, not only providing proximal anchorage for improved stride efficiency but also serving similar function as a cutting balloon. Under the actuation of an external magnetic field, the proposed MSCRs demonstrate the ability to traverse bifurcations and tortuous paths, indicating their potential for dexterous flexibility in pathological vessels. Full article
(This article belongs to the Special Issue Design of Smart Endorobots: Actuators, Sensors and Control Strategies)
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Figure 1
<p>Harmonic MSCRs (magnetic soft continuum robots) feature a flexible magnetic pair tip that (<b>A</b>) realizes caterpillar-style locomotion gait while the multi-magnetic tip enhances flexibility and reduces bending stiffness for augmented maneuverability; (<b>B</b>) incorporates a kirigami surface, which provides proximal support; (<b>C</b>) can inhibit buckling; (<b>D</b>) can possess tortuosity, allowing for complex path navigation; (<b>E</b>) can realize augmented maneuverability.</p>
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<p>Illustration of a catheterization robot featuring a head equipped with magnetic spherical chains, a caterpillar-style body capable of inducing harmonic responses through a magnetic sinusoidal mechanism, and a tail also incorporating magnetic spherical chains that allow for the adjustment of the robot’s deformation style.</p>
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<p>Caterpillar-inspired robot design for anchor push–anchor pull locomotion gait and calculation model for magnetic bending torque.</p>
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<p>Bending torque comparative analysis for axial magnetization and diametrical magnetization.</p>
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<p>Magnetic sinusoidal mechanism: actuation spherical magnet, sinusoidal mechanism, and calculation outcome for bio-inspired robot.</p>
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<p>Fabrication procedure of kirigami skin by CAD design and 2D-3D transformation.</p>
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<p>An experimental platform was developed for the precise measurement of the frictional properties of our kirigami-skin micro-robot.</p>
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<p>A novel magnetic navigation system for vascular interventions involves surgeon A inserting a magnetic guidewire into patient B. A semi-autonomous navigation robot C precisely positions a permanent magnet D within the workspace to guide the guidewire. The proposed guidewire E exhibits a motion gait analogous to an inchworm equipped with kirigami skin F, which is actuated by a sinusoidal magnetic mechanism G.</p>
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<p>EPM navigation system and the magnet distribution between PM and EPM in space.</p>
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<p>Experiment setup for caterpillar-inspired vascular interventional robot.</p>
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<p>Experiment setup and its outcome. (<b>a</b>) the experiment setup. (<b>b</b>) Prototype of the bio-inspired soft robot. (<b>c</b>) Stride analysis geometry model. (<b>d</b>) Experiment scenarios. (<b>e</b>) Experiment outcome.</p>
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32 pages, 8762 KiB  
Article
Selective Inhibition of Deamidated Triosephosphate Isomerase by Disulfiram, Curcumin, and Sodium Dichloroacetate: Synergistic Therapeutic Strategies for T-Cell Acute Lymphoblastic Leukemia in Jurkat Cells
by Luis A. Flores-López, Ignacio De la Mora-De la Mora, Claudia M. Malagón-Reyes, Itzhel García-Torres, Yoalli Martínez-Pérez, Gabriela López-Herrera, Gloria Hernández-Alcántara, Gloria León-Avila, Gabriel López-Velázquez, Alberto Olaya-Vargas, Saúl Gómez-Manzo and Sergio Enríquez-Flores
Biomolecules 2024, 14(10), 1295; https://doi.org/10.3390/biom14101295 (registering DOI) - 13 Oct 2024
Abstract
T-cell acute lymphoblastic leukemia (T-ALL) is a challenging childhood cancer to treat, with limited therapeutic options and high relapse rates. This study explores deamidated triosephosphate isomerase (dTPI) as a novel therapeutic target. We hypothesized that selectively inhibiting dTPI could reduce T-ALL cell viability [...] Read more.
T-cell acute lymphoblastic leukemia (T-ALL) is a challenging childhood cancer to treat, with limited therapeutic options and high relapse rates. This study explores deamidated triosephosphate isomerase (dTPI) as a novel therapeutic target. We hypothesized that selectively inhibiting dTPI could reduce T-ALL cell viability without affecting normal T lymphocytes. Computational modeling and recombinant enzyme assays revealed that disulfiram (DS) and curcumin (CU) selectively bind and inhibit dTPI activity without affecting the non-deamidated enzyme. At the cellular level, treatment with DS and CU significantly reduced Jurkat T-ALL cell viability and endogenous TPI enzymatic activity, with no effect on normal T lymphocytes, whereas the combination of sodium dichloroacetate (DCA) with DS or CU showed synergistic effects. Furthermore, we demonstrated that dTPI was present and accumulated only in Jurkat cells, confirming our hypothesis. Finally, flow cytometry confirmed apoptosis in Jurkat cells after treatment with DS and CU or their combination with DCA. These findings strongly suggest that targeting dTPI represents a promising and selective target for T-ALL therapy. Full article
(This article belongs to the Section Enzymology)
12 pages, 4000 KiB  
Article
Environment Mapping-Based Classification for Reverse Engineering Using Supervised Learning
by Sukhyun Lim
Electronics 2024, 13(20), 4031; https://doi.org/10.3390/electronics13204031 (registering DOI) - 13 Oct 2024
Abstract
With the widespread adoption of 3D scanners, reverse engineering methods for obtaining CAD drawings from physical objects have become increasingly utilized. When converting point data obtained from a 3D scanner into a mesh structure, a smoothing process is typically applied because the point [...] Read more.
With the widespread adoption of 3D scanners, reverse engineering methods for obtaining CAD drawings from physical objects have become increasingly utilized. When converting point data obtained from a 3D scanner into a mesh structure, a smoothing process is typically applied because the point data often contains a lot of noise. However, this can result in the loss of important high-frequency details, or, in cases where significant high-frequency information remains, there are limitations in representing the object with basic geometric shapes. In this paper, a method to address this issue by using environment mapping and supervised learning techniques is proposed. By mapping the object to an environment and then using supervised learning to analyze the data, it can accurately identify the basic geometric shapes. This approach reduces the working time and allows for easier design of complex surfaces that were previously difficult to model. Full article
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<p>When a mesh is classified into primitives (e.g., plane, cylinder, torus, cone, fillet, etc.) through the classification step, CAD editing speed is improved, and the user’s degree of freedom is increased. Additionally, once these primitives are defined, the mesh structure can be created simply, reducing the number of unnecessary calculations in the subsequent steps.</p>
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<p>Traditional RE framework.</p>
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<p>The preprocessed 3D point data is mapped onto a cube environment in the direction of the normal vector N (<b>left</b>). Then, 2D point clouds on the cube map are acquired (<b>right</b>), and on the right only two of the six sides of the cube map are shown for convenience.</p>
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<p>Example of calculating the six lengths (<span class="html-italic">u<sup>max</sup></span>, <span class="html-italic">v<sup>max</sup></span>, <span class="html-italic">d</span><sup>1</sup>~<span class="html-italic">d</span><sup>4</sup>) from the (<span class="html-italic">u</span>, <span class="html-italic">v</span>) coordinate clouds projected onto a cube using EM.</p>
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<p>The learning process (<b>top</b>), and the classification process for feature extraction (<b>bottom</b>).</p>
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<p>Experimental result capture. On the right, when using the method proposed in this paper, relatively more areas were classified as primitives.</p>
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23 pages, 4534 KiB  
Article
Comprehensive Analysis of the 5xFAD Mouse Model of Alzheimer’s Disease Using dMRI, Immunohistochemistry, and Neuronal and Glial Functional Metabolic Mapping
by Emil W. Westi, Saba Molhemi, Caroline Termøhlen Hansen, Christian Stald Skoven, Rasmus West Knopper, Dashne Amein Ahmad, Maja B. Rindshøj, Aishat O. Ameen, Brian Hansen, Kristi A. Kohlmeier and Blanca I. Aldana
Biomolecules 2024, 14(10), 1294; https://doi.org/10.3390/biom14101294 (registering DOI) - 13 Oct 2024
Abstract
Alzheimer’s disease (AD) is characterized by complex interactions between neuropathological markers, metabolic dysregulation, and structural brain changes. In this study, we utilized a multimodal approach, combining immunohistochemistry, functional metabolic mapping, and microstructure sensitive diffusion MRI (dMRI) to progressively investigate these interactions in the [...] Read more.
Alzheimer’s disease (AD) is characterized by complex interactions between neuropathological markers, metabolic dysregulation, and structural brain changes. In this study, we utilized a multimodal approach, combining immunohistochemistry, functional metabolic mapping, and microstructure sensitive diffusion MRI (dMRI) to progressively investigate these interactions in the 5xFAD mouse model of AD. Our analysis revealed age-dependent and region-specific accumulation of key AD markers, including amyloid-beta (Aβ), GFAP, and IBA1, with significant differences observed between the hippocampal formation and upper and lower regions of the cortex by 6 months of age. Functional metabolic mapping validated localized disruptions in energy metabolism, with glucose hypometabolism in the hippocampus and impaired astrocytic metabolism in the cortex. Notably, increased cortical glutaminolysis suggested a shift in microglial metabolism, reflecting an adaptive response to neuroinflammatory processes. While dMRI showed no significant microstructural differences between 5xFAD and wild-type controls, the study highlights the importance of metabolic alterations as critical events in AD pathology. These findings emphasize the need for targeted therapeutic strategies addressing specific metabolic disturbances and underscore the potential of integrating advanced imaging with metabolic and molecular analyses to advance our understanding of AD progression. Full article
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<p>Progressive increase in Aβ accumulation, myelin degeneration, and gliosis in the 5xFAD brains. Representative fluorescence staining images from triple-stainings in brain slices of 5xFAD and WT with (<b>A</b>) Aβ/GFAP/DAPI, (<b>B</b>) IBA1/GFAP/DAPI, and (<b>C</b>) Aβ/MBP/DAPI at 2 (2M) and 6 (6M) month timepoints. (1) 5× magnification (2.02 µm/pixel) microscopy images of brain slices showing subiculum, upper cortex, lower cortex, and white matter. (2) 20× magnification (0.5128 µm/pixel) microscopy images of brain slices showing subiculum. Scale bars indicate 500 µm and 100 µm for upper and lower rows, respectively.</p>
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<p>Quantification of pathological markers in the brains of 5xFAD and WT mice at two ages. Fluorescence microscopy images (represented in <a href="#biomolecules-14-01294-f001" class="html-fig">Figure 1</a>) were quantified, and the corresponding signal derived from the markers (<b>A</b>) Aβ, (<b>B</b>) GFAP, (<b>C</b>) IBA1 and (<b>D</b>) MBP is presented. Four different brain regions are shown: (1) subiculum, (2) upper cortex, (3) lower cortex, and (4) white matter. Each bar graph shows populations of the level of markers in 2M 5xFAD, 2M WT, 6M 5xFAD, and 6M WT mice. The bar graphs are presented as mean percentages of either positive pixels (<b>A</b>–<b>C</b>), or mean gray-scale value (<b>D</b>) ± SD. The number of brain slices is 6 (from 3 independent mice per genotype per age). The statistical comparisons (determined with ANOVA and Tukey’s test) are presented with <span class="html-italic">p</span> values above the bars, with the significant values in bold.</p>
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<p>Cortical acetate metabolism and hippocampal glucose metabolism is selectively affected in 6M 5xFAD brains. (<b>A</b>) Mitochondrial oxidative metabolism of [U-<sup>13</sup>C]glucose (glc, left axes orange bars) or [1,2-<sup>13</sup>C]acetate (ace, right axes, green bars) gives rise to <sup>13</sup>C-enrichment (detected by GC–MS) in TCA cycle intermediates in acutely isolated slices from (<b>B</b>) cerebral cortex or (<b>C</b>) hippocampus incubated with the labeled substrates for 60 min. Molecular carbon labeling (MCL), the weighted average of the carbon labeling in given metabolic intermediates, is presented. [U-<sup>13</sup>C]glucose reflects overall energy metabolism where neurons are the main energy consumers, while [1,2-<sup>13</sup>C]acetate is predominantly metabolized in astrocytes. In the cerebral cortex, overall maintained <sup>13</sup>C-incorporation in TCA cycle metabolites from [U-<sup>13</sup>C]glucose was observed, while lower MCL in intermediates from [1,2-<sup>13</sup>C]acetate was found in 5xFAD mice compared to wild-type (WT) controls. The opposite was observed for the hippocampal slices, where a lower MCL in intermediates resulting from [U-<sup>13</sup>C]glucose metabolism but maintained [1,2-<sup>13</sup>C]acetate was detected in the 5xFAD mice vs. WT. Values represent mean (±) SD (n  =  4 animals). WT animals are represented as circles, while 5xFAD animals are represented as triangles. The statistical significance (determined with Student’s unpaired <span class="html-italic">t</span>-test) is presented with <span class="html-italic">p</span> values above the bars, with significant values in bold.</p>
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<p>Amino acids derived from acetate metabolism are lower in the cortex but unchanged in the hippocampus in 6M 5xFAD brains. (<b>A</b>) Mitochondrial oxidative metabolism of [U-<sup>13</sup>C]glucose (glc, left axes, orange bars) or [1,2-<sup>13</sup>C]acetate (ace, right axes, green bars) gives rise to <sup>13</sup>C-enrichment (detected by GC–MS) in TCA cycle intermediates and derived amino acids in acutely isolated slices from (<b>B</b>) cerebral cortex or (<b>C</b>) hippocampus incubated with the labeled substrates for 60 min. Molecular carbon labeling (MCL), the weighted average of the carbon labeling in given metabolic intermediates, is presented. [U-<sup>13</sup>C]glucose reflects overall energy metabolism where neurons are the main energy consumers, while [1,2-<sup>13</sup>C]acetate is predominantly metabolized in astrocytes. In the cerebral cortex, overall maintained <sup>13</sup>C-incorporation in TCA cycle-derived amino acids from [U-<sup>13</sup>C]glucose was observed, while lower MCL in amino acids from [1,2-<sup>13</sup>C]acetate metabolism was found in 5xFAD mice compared to wild-type (WT) controls. In hippocampal slices, a maintained MCL in amino acids resulting from [U-<sup>13</sup>C]glucose and [1,2-<sup>13</sup>C]acetate metabolism was detected in the 5xFAD mice vs. WT. Values represent mean (±) SD (n  =  4 animals). WT animals are represented as circles, while 5xFAD animals are represented as triangles. The statistical significance (determined with Student’s unpaired <span class="html-italic">t</span>-test) is presented with <span class="html-italic">p</span> values above the bars, with significant values in bold.</p>
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<p>Glutamine uptake is unchanged while its metabolism is higher in the 5xFAD cortex. (<b>A</b>) Uptake and metabolism of [U-<sup>13</sup>C]glutamine (gln) gives rise to <sup>13</sup>C-enrichment (detected by GC–MS) in glutamate, GABA, and TCA cycle intermediates in acutely isolated slices from (<b>B</b>) cerebral cortex or (<b>C</b>) hippocampus incubated with the labeled substrates for 60 min. <sup>13</sup>C-enrichment from direct glutamine metabolism is presented as M + X labeling % (X = number of <sup>13</sup>C-carbons in a given molecule). In the cerebral cortex, overall maintained <sup>13</sup>C-incorporation in amino acids from [U-<sup>13</sup>C]gln was observed, while higher labeling was detected in most TCA cycle intermediates in 5xFAD mice compared to wild-type (WT) controls, suggesting increased glutaminolysis. In hippocampal slices, a maintained labeling in amino acids and TCA cycle intermediates resulting from [U-<sup>13</sup>C]gln metabolism, with the exception of fumarate, was detected in the 5xFAD mice vs. WT. Values represent mean (±) SD (n  =  4 animals). WT animals are represented as circles, while 5xFAD animals are represented as triangles. The statistical significance (determined with Student’s unpaired <span class="html-italic">t</span>-test) is presented with <span class="html-italic">p</span> values above the bars, with significant values in bold.</p>
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<p>The average mean diffusivity (MD) within each region of interest (ROI) was decreased in 5xFAD brains of both age groups. The MD was found consistently decreased in all ROIs of 5xFAD brains compared to WT brains. However, this difference between genotypes was not statistically significant. Additionally, while a small age-related increase in MD was observed in all ROIs for both genotypes, this difference was mainly evident in 5xFAD brains. Group means with 95% confidence intervals are superimposed on the individual observations. 2M = 2-month-old, 6M = 6-month-old. Sub = subiculum, CA = cornu ammonis of the hippocampal formation, hip = hippocampus, CC = corpus callosum, WM = white matter, LC = lower cortex, UC = upper cortex, and neo = neocortex.</p>
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<p>6M 5xFAD brains exhibited decreased averaged mean kurtosis (MK) in all regions of interest (ROIs). While the differences in MK between genotypes of 2-month-old (2M) brains varied between ROIs, a small but consistent decrease was observed in the 6-month-old (6M) 5xFAD brains compared to WT brains. This difference was not statistically significant. An age-related increase was observed in the ROIs of both genotypes, although less pronounced in 5xFAD brains. This age difference was not statistically different either. Group means with 95% confidence intervals are superimposed on the individual observations. Sub = subiculum, CA = cornu ammonis of the hippocampal formation, hip = hippocampus, CC = corpus callosum, WM = white matter, LC = lower cortex, UC = upper cortex, and neo = neocortex.</p>
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<p>The relative volume of all ROIs was unchanged in 5xFAD brains. No difference was observed in the relative volume of the ROIs between genotypes. A statistically significant age × ROI interaction was observed. However, the simple main effects analysis found no statistically significant effect of age in any of the ROIs. The dotted line indicates that LC, UC, and neo are plotted against the right y-axis. Group means with 95% confidence intervals are superimposed on the individual observations. 2M = 2-month-old, 6M = 6-month-old. Sub = subiculum, CA = cornu ammonis of the hippocampal formation, hip = hippocampus, CC = corpus callosum, WM = white matter, LC = lower cortex, UC = upper cortex, and neo = neocortex.</p>
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22 pages, 2514 KiB  
Article
Specialized Pro-Resolving Lipid Mediators Distinctly Modulate Silver Nanoparticle-Induced Pulmonary Inflammation in Healthy and Metabolic Syndrome Mouse Models
by Arjun Pitchai, Akshada Shinde, Jenna N. Swihart, Kiley Robison and Jonathan H. Shannahan
Nanomaterials 2024, 14(20), 1642; https://doi.org/10.3390/nano14201642 (registering DOI) - 13 Oct 2024
Abstract
Individuals with chronic diseases are more vulnerable to environmental inhalation exposures. Although metabolic syndrome (MetS) is increasingly common and is associated with susceptibility to inhalation exposures such as particulate air pollution, the underlying mechanisms remain unclear. In previous studies, we determined that, compared [...] Read more.
Individuals with chronic diseases are more vulnerable to environmental inhalation exposures. Although metabolic syndrome (MetS) is increasingly common and is associated with susceptibility to inhalation exposures such as particulate air pollution, the underlying mechanisms remain unclear. In previous studies, we determined that, compared to a healthy mouse model, a mouse model of MetS exhibited increased pulmonary inflammation 24 h after exposure to AgNPs. This exacerbated response was associated with decreases in pulmonary levels of specific specialized pro-resolving mediators (SPMs). Supplementation with specific SPMs that are known to be dysregulated in MetS may alter particulate-induced inflammatory responses and be useful in treatment strategies. Our current study hypothesized that administration of resolvin E1 (RvE1), protectin D1 (PD1), or maresin (MaR1) following AgNP exposure will differentially regulate inflammatory responses. To examine this hypothesis, healthy and MetS mouse models were exposed to either a vehicle (control) or 50 μg of 20 nm AgNPs via oropharyngeal aspiration. They were then treated 24 h post-exposure with either a vehicle (control) or 400 ng of RvE1, PD1, or MaR1 via oropharyngeal aspiration. Endpoints of pulmonary inflammation and toxicity were evaluated three days following AgNP exposure. MetS mice that were exposed to AgNPs and received PBS treatment exhibited significantly exacerbated pulmonary inflammatory responses compared to healthy mice. In mice exposed to AgNPs and treated with RvE1, neutrophil infiltration was reduced in healthy mice and the exacerbated neutrophil levels were decreased in the MetS model. This decreased neutrophilia was associated with decreases in proinflammatory cytokines’ gene and protein expression. Healthy mice treated with PD1 did not demonstrate alterations in AgNP-induced neutrophil levels compared to mice not receiving treat; however, exacerbated neutrophilia was reduced in the MetS model. These PD1 alterations were associated with decreases in proinflammatory cytokines, as well as elevated interleukin-10 (IL-10). Both mouse models receiving MaR1 treatment demonstrated reductions in AgNP-induced neutrophil influx. MaR1 treatment was associated with decreases in proinflammatory cytokines in both models and increases in the resolution inflammatory cytokine IL-10 in both models, which were enhanced in MetS mice. Inflammatory responses to particulate exposure may be treated using specific SPMs, some of which may benefit susceptible subpopulations. Full article
(This article belongs to the Special Issue Advances in Nanotoxicology: Health and Safety)
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<p>Experiment design timeline. Mice were fed a healthy or high-fat western diet for 14 weeks and exposed to either water (control) or AgNPs (50 µg) via oropharyngeal aspiration; 24 h post-exposure, mice were treated with saline (control) or 400 ng of a lipid resolution mediator (RvE1, PD1, or MaR1) via oropharyngeal aspiration. Endpoints associated with inflammation and lipid metabolism were examined at 2 days following treatment.</p>
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<p>Characterization of (<b>A</b>) body weight and serum levels of (<b>B</b>) high-density lipoprotein, (<b>C</b>) low-density lipoprotein, and (<b>D</b>) total cholesterol in healthy and MetS mouse models following 14 weeks of either a healthy or high-fat western diet (HFW diet) and 3 days after oropharyngeal aspiration exposure to pharmaceutical grade sterile water (vehicle) or 50 μg of AgNPs. Subsets of mice were treated with sterile saline (vehicle) or 400 ng of individual SPMs (RvE1, PD1, or MaR1) 24 h post-exposure. Values are expressed as mean ± S.E.M. # disease model, and <span>$</span> treatment (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>AgNP exposure and modulation by distinct SPM treatment on BALF: (<b>A</b>) total protein, (<b>B</b>) total cell counts, (<b>C</b>) macrophage counts, and (<b>D</b>) neutrophil counts from healthy and MetS mice; 24 h following oropharyngeal aspiration of pharmaceutical grade sterile water (control) or 50 μg of AgNPs in sterile water, mice were treated via oropharyngeal aspiration with 400 ng of individual SPMs (RvE1, PD1, or MaR1) or sterile saline (vehicle). Endpoints were evaluated at 3 days post-AgNP exposure. Values are expressed as mean ± S.E.M. * AgNP exposure, # disease model, and <span>$</span> treatment (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>AgNP exposure and modulation by distinct SPM treatment on the pulmonary gene expression of inflammatory factors including (<b>A</b>) (C-C motif) ligand 2 (CCL2), (<b>B</b>) interleukin-6 (IL-6), (<b>C</b>) chemokine (C-X-C motif) ligand 1 (CXCL1), (<b>D</b>) chemokine (C-X-C motif) ligand 2 (CXCL2), (<b>E</b>) tumor necrosis factor-α (TNF-α), and (<b>F</b>) interleukin-10 (IL-10) from healthy and MetS mice; 24 h following oropharyngeal aspiration of pharmaceutical grade sterile water (control) or 50 μg of AgNPs in sterile water, mice were treated via oropharyngeal aspiration with 400 ng of individual SPMs (RvE1, PD1, or MaR1) or sterile saline (vehicle). Endpoints were evaluated at 3 days post-AgNP exposure. Values are expressed as mean ± S.E.M. * AgNP exposure, # disease model, and <span>$</span> treatment (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>AgNP exposure and modulation by distinct SPM treatment on pulmonary lipid metabolism gene expression, including (<b>A</b>) <span class="html-italic">phospholipase A2</span> (<span class="html-italic">iPLA2</span>), (<b>B</b>) <span class="html-italic">arachidonate 5-lipoxygenase</span> (<span class="html-italic">ALOX-5</span>), (<b>C</b>) <span class="html-italic">arachidonate 15-lipoxygenase</span> (<span class="html-italic">ALOX-15</span>), (<b>D</b>) <span class="html-italic">cyclooxygenase 2</span> (<span class="html-italic">COX 2</span>), and (<b>E</b>) <span class="html-italic">epoxide hydrolase 2</span> (<span class="html-italic">Ephx2</span>) from healthy and MetS mice; 24 h following oropharyngeal aspiration of pharmaceutical grade sterile water (control) or 50 μg of AgNPs in sterile water, mice were treated via oropharyngeal aspiration with 400 ng of individual SPMs or sterile saline (vehicle). Endpoints were evaluated at 3 days post-AgNP exposure. Values are expressed as mean ± S.E.M. * AgNP exposure, # disease model, and <span>$</span> treatment (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>AgNP exposure and modulation by distinct SPM treatment on pulmonary lipid receptor gene expression including (<b>A</b>) the RvE1 receptor, <span class="html-italic">chemerin receptor 23</span> (<span class="html-italic">ChemR23</span>), (<b>B</b>) the PD1 receptor, <span class="html-italic">G protein-coupled receptor 37</span> (<span class="html-italic">GPR37</span>), and (<b>C</b>) the MaR1 receptor, <span class="html-italic">leucine-rich repeat containing G protein-coupled receptor 6</span> (<span class="html-italic">LGR6</span>) from healthy and MetS mice; 24 h following oropharyngeal aspiration of pharmaceutical grade sterile water (control) or 50 μg of AgNPs in sterile water, mice were treated via oropharyngeal aspiration with 400 ng of individual SPMs or sterile saline (vehicle). Endpoints were evaluated at 3 days post-AgNP exposures. Values are expressed as mean ± S.E.M. * AgNP exposure, # disease model, and <span>$</span> treatment (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>AgNP exposure and modulation by distinct SPM treatment on BALF inflammatory cytokine and chemokine levels including (<b>A</b>) chemokine (C-X-C motif) ligand 2 (CXCL2), (<b>B</b>) interleukin-6 (IL-6), and (<b>C</b>) interleukin-10 (IL-10) from healthy and MetS mice; 24 h following oropharyngeal aspiration of pharmaceutical grade sterile water (control) or 50 μg of AgNPs in sterile water, mice were treated via oropharyngeal aspiration with 400 ng of individual SPMs or sterile saline (vehicle). Endpoints were evaluated at 3 days post-AgNP exposure. Values are expressed as mean ± S.E.M. * AgNP exposure, # disease model, and <span>$</span> treatment (<span class="html-italic">p</span> &lt; 0.05).</p>
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13 pages, 4334 KiB  
Article
Limited Alleviation of Lysosomal Acid Lipase Deficiency by Deletion of Matrix Metalloproteinase 12
by Martin Buerger, Melina Amor, Alena Akhmetshina, Valentina Bianco, Bianca Perfler, Armin Zebisch, Thomas Weichhart and Dagmar Kratky
Int. J. Mol. Sci. 2024, 25(20), 11001; https://doi.org/10.3390/ijms252011001 (registering DOI) - 13 Oct 2024
Abstract
Lysosomal acid lipase (LAL) is the only known enzyme that degrades cholesteryl esters and triglycerides at an acidic pH. In LAL deficiency (LAL-D), dysregulated expression of matrix metalloproteinase 12 (MMP-12) has been described. The overexpression of MMP-12 in myeloid lineage cells causes an [...] Read more.
Lysosomal acid lipase (LAL) is the only known enzyme that degrades cholesteryl esters and triglycerides at an acidic pH. In LAL deficiency (LAL-D), dysregulated expression of matrix metalloproteinase 12 (MMP-12) has been described. The overexpression of MMP-12 in myeloid lineage cells causes an immune cell dysfunction resembling that of Lal knockout (Lal KO) mice. Both models develop progressive lymphocyte dysfunction and expansion of myeloid-derived suppressor (CD11b+ Gr-1+) cells. To study whether MMP-12 might be a detrimental contributor to the pathology of LAL-D, we have generated Lal/Mmp12 double knockout (DKO) mice. The phenotype of Lal/Mmp12 DKO mice closely resembled that of Lal KO mice, while the weight and morphology of the thymus were improved in Lal/Mmp12 DKO mice. Cytological examination of blood smears showed a mildly reversed lymphoid-to-myeloid shift in DKO mice. Despite significant decreases in CD11b+ Ly6G+ cells in the peripheral blood, bone marrow, and spleen of Lal/Mmp12 DKO mice, the hematopoietic bone marrow progenitor compartment and markers for neutrophil chemotaxis were unchanged. Since the overall severity of LAL-D remains unaffected by the deletion of Mmp12, we conclude that MMP-12 does not represent a viable target for treating the inflammatory pathology in LAL-D. Full article
(This article belongs to the Special Issue Peroxisome and Lysosome in Health and Disease)
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Figure 1

Figure 1
<p>Phenotype of <span class="html-italic">Lal/Mmp12</span> DKO mice. Male 30-week-old chow-diet-fed WT, <span class="html-italic">Lal</span> KO, and <span class="html-italic">Lal/Mmp12</span> DKO mice were fasted for 6 h. (<b>A</b>) Body weight. (<b>B</b>) Weight of subcutaneous white adipose tissue (sWAT) and brown adipose tissue (BAT), normalized to brain weight; WT mice were arbitrarily set to 1. (<b>C</b>) Mean diameter of adipocytes from sWAT paraffin sections. (<b>D</b>) Liver weight normalized to brain weight; WT mice were arbitrarily set to 1. (<b>E</b>) Hepatic mRNA expression of macrophage markers (<span class="html-italic">Emr1</span> and <span class="html-italic">Cd68</span>) relative to <span class="html-italic">Hprt</span> expression. (<b>F</b>) Hepatic lipid parameters. (<b>G</b>) Representative images of H&amp;E-stained liver sections. Scale bars, 100 µm. Asterisks indicate the granuloma-like accumulation of lipid-laden macrophages. Hepatic mRNA expression of (<b>H</b>) <span class="html-italic">Mmp12</span> and (<b>I</b>) inflammation/chemotactic markers (<span class="html-italic">Tnf</span>, <span class="html-italic">Il1b</span>, and <span class="html-italic">Ccl2</span>) relative to <span class="html-italic">Hprt</span> expression. Plasma concentrations of (<b>J</b>) aspartate aminotransferase (AST), alanine aminotransferase (ALT), and (<b>K</b>) serum amyloid A (SAA). Data are shown as means (n = 4–8) + SD. <sup>###</sup> <span class="html-italic">p</span> ≤ 0.001 for the comparison between <span class="html-italic">Lal</span> KO and <span class="html-italic">Lal/Mmp12</span> DKO mice.</p>
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<p>Minor changes in total blood cell counts but ameliorated thymus weight and morphology in <span class="html-italic">Lal/Mmp12</span> DKO mice. Complete blood counts in peripheral blood collected from 28–32-week-old chow-diet-fed male WT, <span class="html-italic">Mmp12</span>, <span class="html-italic">Lal</span> KO, and <span class="html-italic">Lal/Mmp12</span> DKO mice for (<b>A</b>) total leukocytes and (<b>B</b>) thrombocytes. (<b>C</b>) Hemoglobin concentrations. (<b>D</b>) The frequency of myeloid and lymphoid cells determined by cytological examination of Giemsa-stained blood smears. (<b>E</b>) Thymus weight normalized to brain weight; WT mice were arbitrarily set to 1. (<b>F</b>) Representative images of H&amp;E-stained thymus sections. Scale bars, 100 µm. Red arrows indicate the accumulation of lipid-laden macrophages. Data are shown as means (n = 4–9) + SD. <sup>†</sup> <span class="html-italic">p</span> &lt; 0.05 for the comparison between WT and <span class="html-italic">Mmp12</span> KO mice; <sup>#</sup> <span class="html-italic">p</span> &lt; 0.05 and <sup>##</sup> <span class="html-italic">p</span> ≤ 0.01 for the comparison between <span class="html-italic">Lal</span> KO and <span class="html-italic">Lal/Mmp12</span> DKO mice.</p>
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<p>Reduced CD11b+ Ly6G+ counts in blood, bone marrow, and spleen, but no changes in the hematopoietic progenitor compartment of <span class="html-italic">Lal/Mmp12</span> DKO mice. (<b>A</b>) Representative flow cytometric plots and their quantification, depicting a decreased CD11b+ Ly6G+ fraction in peripheral blood, bone marrow, and spleen of <span class="html-italic">Lal/Mmp12</span> DKO compared to <span class="html-italic">Lal</span> KO mice. (<b>B</b>) Spleen weight normalized to brain weight; WT mice were arbitrarily set to 1. (<b>C</b>) The content of Lin- Sca1+ c-Kit+ (LSK) and Lin- c-Kit+ (LK) and (<b>D</b>) progenitor cells [common myeloid progenitors (CMPs), granulocyte–macrophage progenitors (GMPs), megakaryocyte–erythrocyte progenitor cells (MEPs)] shown as % of 7-AAD lineage-negative bone marrow cells. Data are shown as means (n = 4–10) + SD. ** <span class="html-italic">p</span> &lt; 0.01 and *** <span class="html-italic">p</span> ≤ 0.001 for the comparison between WT and Lal KO mice; <sup>#</sup> <span class="html-italic">p</span> ≤ 0.05 and <sup>##</sup> <span class="html-italic">p</span> ≤ 0.01 for the comparison between <span class="html-italic">Lal</span> KO and <span class="html-italic">Lal/Mmp12</span> DKO mice.</p>
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<p>Altered spleen morphology but unchanged neutrophil chemotaxis and lymphocyte markers in <span class="html-italic">Lal/Mmp12</span> DKO mice. (<b>A</b>) Representative images of H&amp;E-stained spleen sections. Green arrows indicate white pulps; red arrows indicate red pulps. Scale bars, 100 µm. Gene expression of (<b>B</b>) the macrophage marker <span class="html-italic">Cd68</span>, (<b>C</b>) <span class="html-italic">Mmp12</span>, (<b>D</b>,<b>E</b>) neutrophil markers (<span class="html-italic">Ly6g</span> and <span class="html-italic">Elane</span>), (<b>F</b>–<b>H</b>) chemokine receptors (<span class="html-italic">Cxcr1</span>, <span class="html-italic">Cxcr2</span>, and <span class="html-italic">Cxcr4</span>), (<b>I</b>–<b>K</b>) chemokine ligands (<span class="html-italic">Cxcl1</span>, <span class="html-italic">Cxcl2</span>, and <span class="html-italic">Cxcl5</span>), and (<b>L</b>,<b>M</b>) lymphocyte markers (<span class="html-italic">Cd3e</span> and <span class="html-italic">B220</span>) relative to <span class="html-italic">Ppia</span> expression. (<b>N</b>) Immunoblot analysis showing the absence of <span class="html-italic">CD3e</span> expression in the spleen of <span class="html-italic">Lal</span> KO (LKO) and <span class="html-italic">Lal/Mmp12</span> DKO mice. Calnexin was used as loading control. Data are shown as means (n = 3–5) + SD. * <span class="html-italic">p</span> ≤ 0.05, ** <span class="html-italic">p</span> ≤ 0.01, and *** <span class="html-italic">p</span> ≤ 0.001 for the comparison between WT and <span class="html-italic">Lal</span> KO mice; <sup>###</sup> <span class="html-italic">p</span> ≤ 0.001 for the comparison between <span class="html-italic">Lal</span> KO and <span class="html-italic">Lal/Mmp12</span> DKO mice.</p>
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34 pages, 8858 KiB  
Review
Studying the Defects in Spinel Compounds: Discovery, Formation Mechanisms, Classification, and Influence on Catalytic Properties
by Tetiana Tatarchuk
Nanomaterials 2024, 14(20), 1640; https://doi.org/10.3390/nano14201640 (registering DOI) - 12 Oct 2024
Abstract
Spinel ferrites demonstrate extensive applications in different areas, like electrodes for electrochemical devices, gas sensors, catalysts, and magnetic adsorbents for environmentally important processes. However, defects in the real spinel structure can change the many physical and chemical properties of spinel ferrites. Although the [...] Read more.
Spinel ferrites demonstrate extensive applications in different areas, like electrodes for electrochemical devices, gas sensors, catalysts, and magnetic adsorbents for environmentally important processes. However, defects in the real spinel structure can change the many physical and chemical properties of spinel ferrites. Although the number of defects in a crystal spinel lattice is small, their influence on the vast majority of physical properties could be really decisive. This review provides an overview of the structural characteristics of spinel compounds (e.g., CoFe2O4, NiFe2O4, ZnFe2O4, Fe3O4, γ–Fe2O3, Co3O4, Mn3O4, NiCo2O4, ZnCo2O4, Co2MnO4, etc.) and examines the influence of defects on their properties. Attention was paid to the classification (0D, 1D, 2D, and 3D defects), nomenclature, and the formation of point and surface defects in ferrites. An in-depth description of the defects responsible for the physicochemical properties and the methodologies employed for their determination are presented. DFT as the most common simulation approach is described in relation to modeling the point defects in spinel compounds. The significant influence of defect distribution on the magnetic interactions between cations, enhancing magnetic properties, is highlighted. The main defect-engineering strategies (direct synthesis and post-treatment) are described. An antistructural notation of active centers in spinel cobalt ferrite is presented. It is shown that the introduction of cations with different charges (e.g., Cu(I), Mn(II), Ce(III), or Ce(IV)) into the cobalt ferrite spinel matrix results in the formation of various point defects. The ability to predict the type of defects and their impact on material properties is the basis of defect engineering, which is currently an extremely promising direction in modern materials science. Full article
(This article belongs to the Special Issue Magnetization and Magnetic Disorder at the Nanoscale)
25 pages, 2413 KiB  
Article
Object Detection Algorithm for Citrus Fruits Based on Improved YOLOv5 Model
by Yao Yu, Yucheng Liu, Yuanjiang Li, Changsu Xu and Yunwu Li
Agriculture 2024, 14(10), 1798; https://doi.org/10.3390/agriculture14101798 (registering DOI) - 12 Oct 2024
Abstract
To address the challenges of missed and false detections in citrus fruit detection caused by environmental factors such as leaf occlusion, fruit overlap, and variations in natural light in hilly and mountainous orchards, this paper proposes a citrus detection model based on an [...] Read more.
To address the challenges of missed and false detections in citrus fruit detection caused by environmental factors such as leaf occlusion, fruit overlap, and variations in natural light in hilly and mountainous orchards, this paper proposes a citrus detection model based on an improved YOLOv5 algorithm. By introducing receptive field convolutions with full 3D weights (RFCF), the model overcomes the issue of parameter sharing in convolution operations, enhancing detection accuracy. A focused linear attention (FLA) module is incorporated to improve the expressive power of the self-attention mechanism while maintaining computational efficiency. Additionally, anchor boxes were re-clustered based on the shape characteristics of target objects, and the boundary box loss function was improved to Foal-EIoU, boosting the model’s localization ability. Experiments conducted on a citrus fruit dataset labeled using LabelImg, collected from hilly and mountainous areas, showed a detection precision of 95.83% and a mean average precision (mAP) of 79.68%. This research not only significantly improves detection performance in complex environments but also provides crucial data support for precision tasks such as orchard localization and intelligent picking, demonstrating strong potential for practical applications in smart agriculture. Full article
(This article belongs to the Section Digital Agriculture)
27 pages, 3292 KiB  
Article
Revealing the Diversity of Sequences, Structures, and Targets of Peptides from South China Sea Macrodactyla doreensis Based on Transcriptomics
by Ziqiang Hua, Yanling Liao, Jinxing Fu, Xinru Li, Qianxia Xu, Limin Lin, Meiling Huang and Bingmiao Gao
Mar. Drugs 2024, 22(10), 470; https://doi.org/10.3390/md22100470 (registering DOI) - 12 Oct 2024
Abstract
The South China Sea is rich in sea anemone resources, and the protein and peptide components from sea anemone toxins comprise an important treasure trove for researchers to search for leading compounds. This study conducted a comprehensive transcriptomic analysis of the tentacles and [...] Read more.
The South China Sea is rich in sea anemone resources, and the protein and peptide components from sea anemone toxins comprise an important treasure trove for researchers to search for leading compounds. This study conducted a comprehensive transcriptomic analysis of the tentacles and column of Macrodactyla doreensis and explored the distribution and diversity of proteins and peptides in depth using bioinformatics, initially constructing a putative protein and peptide database. In this database, typical peptide families are identified through amino acid sequence analysis, and their 3D structures and potential biological activities are revealed through AlphaFold2 modeling and molecular docking. A total of 4,239 transcripts were identified, of which the putative protein accounted for 81.53%. The highest content comprised immunoglobulin and a variety of proteases, mainly distributed in the column and related to biological functions. Importantly, the putative peptide accounted for 18.47%, containing ShK domain and Kunitz-type peptides, mainly distributed in the tentacles and related to offensive predatory behavior. Interestingly, 40 putative peptides belonging to eight typical peptide families were identified, and their structures and targets were predicted. This study reveals the diversity and complexity of Macrodactyla doreensis toxins and predicts their structure and targets based on amino acid sequences, providing a feasible approach for research regarding the discovery of peptides with potentially high activity. Full article
11 pages, 4032 KiB  
Article
Between Life and Death: Sea Urchin Embryos Undergo Peculiar DNA Fragmentation after Exposure to Vanadium, Cadmium, Gadolinium, and Selenium
by Chiara Martino and Roberto Chiarelli
Life 2024, 14(10), 1296; https://doi.org/10.3390/life14101296 (registering DOI) - 12 Oct 2024
Abstract
Exogenous DNA damage represents one of the most harmful outcomes produced by environmental, physical, or chemical agents. Here, a comparative analysis of DNA fragmentation was carried out on Paracentrotus lividus sea urchin embryos exposed to four common pollutants of the marine environment: vanadium, [...] Read more.
Exogenous DNA damage represents one of the most harmful outcomes produced by environmental, physical, or chemical agents. Here, a comparative analysis of DNA fragmentation was carried out on Paracentrotus lividus sea urchin embryos exposed to four common pollutants of the marine environment: vanadium, cadmium, gadolinium and selenium. Using the terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay, fragmented DNA was quantified and localized in apoptotic cells mapping whole-mount embryos. This is the first study reporting how different chemicals are able to activate distinctive apoptotic features in sea urchin embryos, categorized as follows: (i) cell-selective apoptosis, showing DNA fragmentation restricted to a subset of extremely damaged cells, acting as an embryo survival mechanism; or (ii) total apoptosis, with fragmented DNA widespread throughout the cells of the entire embryo, leading to its death. Also, this is the first report of the effects of Se exposure on P. lividus sea urchin embryos. These data confirm the TUNEL assay as the most suitable test to study DNA fragmentation in the sea urchin embryo model system. Taken together, this research highlights embryos’ ability to find alternative pathways and set physiological limits for development under stress conditions. Full article
(This article belongs to the Special Issue Ecotoxicity Effects of Metals and Microplastics on Aquatic Organisms)
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<p>Location of the sampling points for <span class="html-italic">Paracentrotus lividus</span> sea urchins in the Favignana island MPA, west coast of Sicily.</p>
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<p>Representative images of 48 h larvae: (<b>A</b>) controls; embryos exposed to 100 μM of (<b>B</b>) vanadium (V); (<b>C</b>) cadmium (Cd); (<b>D</b>) gadolinium (Gd); (<b>E</b>) selenium (Se). Bar: 100 μm.</p>
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<p>Larval body length (BL) detected after 48 h of development (<span class="html-italic">n</span> = 9 ± SD). Treatments with the same letter do not differ (Tukey HSD).</p>
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<p>Fluorescent terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay on whole-mount sea urchin embryos. Images of representative control and treated embryos at 48 h, observed under a fluorescence microscope: fragmented DNA (<b>A1</b>–<b>G1</b>); nuclei stained with propidium iodide (<b>A2</b>–<b>G2</b>); merging of both signals (<b>A3</b>–<b>G3</b>). Control embryo (<b>A1</b>–<b>A3</b>); V-treated embryo (<b>B1</b>–<b>B3</b>); Cd-treated embryo (<b>C1</b>–<b>C3</b>); Gd-treated embryo (<b>D1</b>–<b>D3</b>); Se-treated embryo (<b>E1</b>–<b>E3</b>); negative-control embryo (<b>F1</b>–<b>F3</b>); and Positive-control embryo (<b>G1</b>–<b>G3</b>). Bar = 100 μm.</p>
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<p>Histogram showing fluorescence optical densitometry analysis related to fragmented DNA signals. Data report the quantification of green fluorescence for the entire morphological population (<span class="html-italic">n</span> = 9 ± SD). Treatments with the same letter do not differ (Tukey HSD).</p>
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10 pages, 1857 KiB  
Communication
Distribution Patterns of tfdI and tfdII Gene Clusters and New Insights into the Formation of the Architecture of pJP4, a Canonical 2,4-dichlorophenoxyacetic Acid (2,4-D) Degradation Plasmid
by Timur Iasakov
Int. J. Mol. Sci. 2024, 25(20), 10998; https://doi.org/10.3390/ijms252010998 (registering DOI) - 12 Oct 2024
Abstract
Currently, pJP4 is one of the best-known plasmids for the biodegradation of xenobiotics that mediate the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D), which is associated with serious health and environmental risks. Although the sequencing and proposed theory of pJP4 formation occurred almost 20 years [...] Read more.
Currently, pJP4 is one of the best-known plasmids for the biodegradation of xenobiotics that mediate the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D), which is associated with serious health and environmental risks. Although the sequencing and proposed theory of pJP4 formation occurred almost 20 years ago (2004), pJP4 is still the model object of many studies focused on the biodegradation of 2,4-D. The uniqueness of this plasmid is due to the presence of two evolutionarily distinct gene clusters, tfdI and tfdII, controlling the degradation of 2,4-D. Recent advances in plasmid biology, especially those concerning the characterization of new IncP-1 plasmids and the systematization of tfd gene cluster findings, serve as a basis for proposing new insights into the formation of the clusters’ architecture of the canonical plasmid, pJP4, and their distribution among other plasmids. In the present work, a comparative genomic and phylogenetic in silico study of plasmids with tfdI and tfdII clusters was carried out. The possible initial distribution patterns of tfdI clusters among plasmids of different incompatibility groups (non-IncP-1) and tfdII clusters among IncP-1 plasmids using the IS1071-based composite transposon were revealed. A new theory on the formation of the architecture of the tfdI and tfdII clusters of pJP4 through sequential internal rearrangements, recombination, and ISJP4 insertion, is proposed. In addition, small gene clusters resulting from internal rearrangements of pJP4 (tfdIISA and ORF31/32) served as fingerprints for exploring the distribution of tfdI and tfdII clusters. The revealed patterns and formulated theory extend the frontiers of plasmid biology and will be beneficial for understanding the role of plasmids in bacterial adaptation to xenobiotic-contaminated environments. Full article
(This article belongs to the Section Molecular Microbiology)
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Figure 1

Figure 1
<p>Maximum likelihood (ML) phylogenetic tree of replication initiation proteins TrfA of the IncP-1 plasmids. The IncP-1 plasmid subgroups are designated by Greek letters and highlighted with different colors. The proteins RepA and RepA1 of plasmids RA1 (IncA/C) and NR1 (IncFII), respectively, were used as an outgroup. Bootstrap support values higher than 50% are indicated at branching points. The trees are drawn to scale, with branch lengths measured in the number of amino acid substitutions per site. The scale bar at the bottom of the figure corresponds to 2 amino acid substitutions per 10 amino acids.</p>
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<p>Comparative genomic analysis: (<b>a</b>) comparative genetic structures of the IncP-1 plasmids which contained <span class="html-italic">tfd</span> gene clusters; (<b>b</b>) comparison of <span class="html-italic">tfd</span><sub>I</sub>-containing regions of IncP-1, IncHI2, and IncA/C plasmids. The plasmids and plasmid regions are shown by linear visualization with genes illustrated by labeled arrows, which are colored according to their functions (bottom). White and black unlabeled arrows indicate genes that are not discussed. The direction of the arrows indicates the location of the genes on the plasmid strands (right, forward strand; left, reverse strand). The truncated mobile elements are designated by delta symbol (Δ). The heat key (bottom right) illustrates the intensity of the grayscale-shaded regions according to blastn, which indicates the degree of identity between plasmids and plasmid regions. The scale in kilobase pairs (Kbp) is displayed on the bottom right side.</p>
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<p>Putative distribution patterns of <span class="html-italic">tfd</span> clusters and the scenario of pJP4 plasmid architecture formation: (<b>a</b>) the previous model for the evolution of pJP4, adapted from Trefault et al. (2004) [<a href="#B3-ijms-25-10998" class="html-bibr">3</a>]; (<b>b</b>) the distribution patterns and scenario proposed in the present study. Plasmids are represented by circles, and the resulting evolutionary events by labeled arrows. Clusters and mobile elements acquired by plasmids are indicated by different colors on the plasmid circles. The truncated mobile elements are designated by the asterisk or delta symbol (Δ).</p>
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23 pages, 12010 KiB  
Article
Geological and Engineering Integration Fracturing Design and Optimization Study of Liushagang Formation in Weixinan Sag
by Yinghao Shen, Bing Liu, Hongfeng Jiang, Hong Mao, Mingrui Li and Zhicheng Yang
J. Mar. Sci. Eng. 2024, 12(10), 1821; https://doi.org/10.3390/jmse12101821 (registering DOI) - 12 Oct 2024
Abstract
The Weixinan Sag in the Beibuwan Basin is rich in shale oil resources. However, the reservoirs exhibit rapid phase changes, strong compartmentalization, thin individual layers, and high-frequency vertical variations in the thin interbedded sandstone and mudstone. These factors can restrict the height of [...] Read more.
The Weixinan Sag in the Beibuwan Basin is rich in shale oil resources. However, the reservoirs exhibit rapid phase changes, strong compartmentalization, thin individual layers, and high-frequency vertical variations in the thin interbedded sandstone and mudstone. These factors can restrict the height of hydraulic fracture propagation. Additionally, the low-porosity and low-permeability shale oil reservoirs face challenges such as low production rates and rapid decline. To address these issues, the Plannar3D full 3D fracturing model was used to simulate hydraulic fracture propagation and to study the main controlling factors for fracture propagation in the second member of the Liushagang Formation. Based on the concept of geological–engineering integration, a sweet spot evaluation was conducted to identify reservoirs with relatively better brittleness, reservoir properties, and oil content as the fracturing targets for horizontal wells. The UFM model was then applied to optimize fracturing parameters. This study indicates that the matrix-type oil shale has a high clay mineral content, resulting in a low Young’s modulus and poor brittleness. This makes hydraulic fracture propagation difficult and leads to less effective reservoir stimulation. In contrast, hydraulic fractures propagate more easily in high-brittleness interlayer-type oil shale. Therefore, it is recommended to prioritize the extraction of shale oil from interlayer-type oil shale reservoirs. The difference in interlayer stress is identified as the primary controlling factor for cross-layer fracture propagation in the study area. Based on the concept of geological–engineering integration, a sweet spot evaluation standard was established for the second member of the Liushagang Formation, considering both reservoir quality and engineering quality. Four sweet spot zones of interlayer-type oil shale reservoirs were identified according to this evaluation standard. To achieve uniform fracture initiation, a differentiated segment and cluster design was implemented for certain high-angle sections of well WZ11-6-5d. Interlayer-type oil shale was selected as the fracturing target, and the UFM was used for hydraulic fracture propagation simulation. Fracturing parameters were optimized with a focus on hydraulic fracture characteristics and the estimated ultimate recovery (EUR). The optimization results were as follows: a single-stage length of 50 m, cluster spacing of 15 m, pump injection rate of 10 m3/min, fluid intensity of 25 m3/m, and proppant intensity of 3.5 t/m. The application of these optimized fracturing parameters in field operations resulted in successful fracturing and the achievement of industrial oil flow. Full article
(This article belongs to the Section Geological Oceanography)
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<p>Technology roadmap.</p>
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<p>Three-dimensional geological model in the study area.</p>
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<p>Three-dimensional geomechanical modeling in the study area.</p>
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<p>Ants tracking faults and natural fractures results.</p>
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<p>Simulation results of hydraulic fractures at different perforation positions.</p>
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<p>Results of sweet spot evaluation of three different types of oil shale reservoirs.</p>
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<p>Segment and cluster differentiation design.</p>
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<p>Comparison of hydraulic fracture morphology for different segment lengths.</p>
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<p>EUR simulation results for different subsection segment lengths.</p>
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<p>Fracture reconstruction volume comparison for different cluster spacings.</p>
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<p>EUR simulation results and oil production rate for different cluster spacing schemes.</p>
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<p>Hydraulic fracture morphology of different pumping rates.</p>
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<p>Comparison of hydraulic fracture length and height for different pumping rates.</p>
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<p>Comparison of fracture modification volumes with different fluid intensity.</p>
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<p>EUR simulation results for different fluid intensity.</p>
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<p>The schematic diagram of formation pressure drop in 10 years of production with different proppant intensity.</p>
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<p>EUR simulation results for different proppant intensity.</p>
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<p>Testing daily oil production curves after fracturing.</p>
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<p>Testing daily gas production curves after fracturing.</p>
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14 pages, 6257 KiB  
Article
Degradation-Guided Multi-Modal Fusion Network for Depth Map Super-Resolution
by Lu Han, Xinghu Wang, Fuhui Zhou and Diansheng Wu
Electronics 2024, 13(20), 4020; https://doi.org/10.3390/electronics13204020 (registering DOI) - 12 Oct 2024
Abstract
Depth map super-resolution (DSR) is a technique aimed at restoring high-resolution (HR) depth maps from low-resolution (LR) depth maps. In this process, color images are commonly used as guidance to enhance the restoration procedure. However, the intricate degradation of LR depth poses a [...] Read more.
Depth map super-resolution (DSR) is a technique aimed at restoring high-resolution (HR) depth maps from low-resolution (LR) depth maps. In this process, color images are commonly used as guidance to enhance the restoration procedure. However, the intricate degradation of LR depth poses a challenge, and previous image-guided DSR approaches, which implicitly model the degradation in the spatial domain, often fall short of producing satisfactory results. To address this challenge, we propose a novel approach called the Degradation-Guided Multi-modal Fusion Network (DMFNet). DMFNet explicitly characterizes the degradation and incorporates multi-modal fusion in both spatial and frequency domains to improve the depth quality. Specifically, we first introduce the deep degradation regularization loss function, which enables the model to learn the explicit degradation from the LR depth maps. Simultaneously, DMFNet converts the color images and depth maps into spectrum representations to provide comprehensive multi-domain guidance. Consequently, we present the multi-modal fusion block to restore the depth maps by leveraging both the RGB-D spectrum representations and the depth degradation. Extensive experiments demonstrate that DMFNet achieves state-of-the-art (SoTA) performance on four benchmarks, namely the NYU-v2, Middlebury, Lu, and RGB-D-D datasets. Full article
(This article belongs to the Special Issue Advances in Data-Driven Artificial Intelligence)
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