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. Author manuscript; available in PMC: 2016 Nov 1.
Published in final edited form as: Arterioscler Thromb Vasc Biol. 2015 Oct 1;35(11):2391–2400. doi: 10.1161/ATVBAHA.115.306474

Figure 2. EDA+-FN enhances macrophage cells infiltration but not foam cell formation.

Figure 2

Figure 2

A. Top panel shows representative photomicrographs stained for macrophages (mac-3 positive cells stained as brown) and counterstained with hematoxylin (blue). Scale bar = 200μm. Bottom panel shows quantification. N=8 mice/group. Each dot represents a single mouse. Value for each mouse represents a mean of 16 fields from 4 serial sections (each 80 mm apart, beginning at the aortic valve leaflets and spanning 320 mm). B. Left panel shows staining of purified bone marrow-derived macrophages from female EDA−/−Apoe−/−, EDAfl/flApoe−/−, and control Apoe−/− mice with Oil Red O 24 hour after incubating them with acetylated LDL (100 μg/ml). Right panel shows quantification of total cholesterol. C. Left panel shows staining of purified bone marrow-derived macrophages from female EDA−/−Apoe−/− mice with Oil Red O 24 hour after incubating them with LDL (50 μg/ml) under different conditions. Right panel shows quantification of total cholesterol. Values are mean ± SEM. N=5-6 mice/group. NS= non significant.

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