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Image Search Results
Journal: bioRxiv
Article Title: Resolvin D2/GPR18 signaling enhances monocytic myeloid-derived suppressor cell function to mitigate abdominal aortic aneurysm formation
doi: 10.1101/2024.02.23.581672
Figure Lengend Snippet: RvD2 administration decreases aortic aneurysm phenotype and preserves morphology to mitigate AAA formation. A , Schematic description of murine topical elastase model with RvD2 treatments. Mice were divided into three groups and treated with either heat-inactivated elastase or elastase on day 0. Mice were then administered either vehicle or RvD2. Aortic diameter was measured on day 14 and tissue harvested for additional analysis. B , RvD2 treated mice demonstrated a significant decrease in aortic diameter compared to vehicle treated mice; *p<0.001 vs. other groups; n=10-20 per group). C , Representative images of aortic phenotype in the respective groups. D , Comparative histology performed on day 14 indicates that elastase-treated mice administered with RvD2 have a marked increase in smooth muscle cell α-actin (SM-α actin) expression, decrease in elastic fiber disruption (Verhoeff-Van Gieson staining for elastin) as well as neutrophil (PMN) and macrophage (Mac-2) infiltration, compared to elastase-treated WT mice alone (n=5 per group). Representative histological images in the respective groups with arrows indicate areas of immunostaining. E , Quantification of histological staining in respective groups; n=5 per group; *p<0.02 vs. other groups.
Article Snippet: Slides of aortic cross-sections were prepared and stained for elastin (Van Gieson’s Solution, catalog no. s289; Poly Scientific R&D Systems, Bay Shore, NY) smooth muscle actin (monoclonal anti-actin α-smooth muscle, Sigma Aldrich, St. Louis, MO),
Techniques: Expressing, Disruption, Staining, Immunostaining
Journal: bioRxiv
Article Title: Resolvin D2/GPR18 signaling enhances monocytic myeloid-derived suppressor cell function to mitigate abdominal aortic aneurysm formation
doi: 10.1101/2024.02.23.581672
Figure Lengend Snippet: In vivo GPR18 knockdown reduces the protective effect of RvD2. A , GPR18-siRNA treatment of WT mice demonstrated a significant increase in aortic diameter as compared to control (c)-siRNA treated mice after administration of RvD2 in respective groups (*p=0.004, n=12-13 per group). B , Representative images of aortic phenotype in respective groups. C, Expression of smooth muscle-α actin is significantly increased, and elastin fragmentation as well as macrophage and neutrophil infiltration in aortic tissue are significantly decreased in mice treated with c-siRNA+RvD2 compared to mice treated with GPR18 siRNA+RvD2 (n=5 per group). Arrows indicate areas of immunostaining. D, Quantification of histological staining in respective groups; n=5 per group; *p<0.01 vs. other groups.
Article Snippet: Slides of aortic cross-sections were prepared and stained for elastin (Van Gieson’s Solution, catalog no. s289; Poly Scientific R&D Systems, Bay Shore, NY) smooth muscle actin (monoclonal anti-actin α-smooth muscle, Sigma Aldrich, St. Louis, MO),
Techniques: In Vivo, Knockdown, Control, Expressing, Immunostaining, Staining