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FGFR1 and TGFβ signaling activity in smooth muscle cells in a mouse atherosclerosis model
FGFR1 and TGFβ signaling activity in smooth muscle cells in a mouse atherosclerosis model ADissected mouse aorta demonstrating lipid‐rich plaques in brachiocephalic artery after 4 months of high‐fat diet compared to the normal diet in Apoe−/− mice. Panels b, d are cross sections of brachiocephalic artery from a, c stained with Oil Red O. L: lumen. Scale bar: 4 mm. n = 3 mice per group.BHistological analysis of mouse normal artery or atherosclerotic plaque in brachiocephalic artery with anti‐SM α‐actin, anti‐Notch3, and anti‐SM‐MHC antibodies. Nuclei were counterstained with DAPI (blue). L: lumen. Scale bar: 62 μm. n = 3 mice per group.C–FAnalysis of brachiocephalic artery of Apoe−/− mice maintained for 4 months on either normal or high‐fat diet using anti‐CD31 (green), anti‐p‐FGFR1 (red; C), anti‐FGFR1 (red; D), anti‐p‐Smad2 (red; E), and anti‐p‐Smad3 (red; F) antibodies. Nuclei were counterstained with DAPI (blue). Scale bar: 62 μm. L: lumen. M: media. n = 6 mice per group.G–JQuantification of the number of medial smooth muscle cells expressing p‐FGFR1, FGFR1, p‐Smad2, and p‐Smad3. ND: normal diet. HFD: high‐fat diet.Data information: All data shown as means ± SD (***P < compared to ND, NS: not significant compared to ND; unpaired two‐tailed Student's t‐test). A full table of P‐values for this figure is shown in Appendix Table S1. Pei‐Yu Chen et al. EMBO Mol Med. 2016;emmm © as stated in the article, figure or figure legend
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