Figure 5
Figure 5. VWF is required for VSMC coverage in developmental angiogenesis. (A) Representative images of retinas undergoing early postnatal retinal developmental angiogenesis at 3 different time points: P3, P5, and P7. Retinas were immunostained with CD31 (red) to label the endothelium and αSMA to label VSMCs (green). (B) VWF KO mice have significantly less VSMC coverage compared with age-matched controls, measured along each artery as a percentage of the outgrowth of the vascular plexus (dotted lines). Arterial coverage is reduced 37% at P3, 21% at P5, and 17% at P7. Values represent means ± SEM. C57BL/6 (n = 12 [P3], n = 23 [P5], n = 19 [P7]), VWF KO (n = 14 [P3], n = 25 [P5], n = 14 [P7]), where n is the number of retinas analyzed. P = 9.3 × 10−4 (P3), P = 1.7 × 10−9 (P5), P = 7.3 × 10−3 (P7). Scale bars: 150 μm (P3), 300 μm (P5), and 600 μm (P7).

VWF is required for VSMC coverage in developmental angiogenesis. (A) Representative images of retinas undergoing early postnatal retinal developmental angiogenesis at 3 different time points: P3, P5, and P7. Retinas were immunostained with CD31 (red) to label the endothelium and αSMA to label VSMCs (green). (B) VWF KO mice have significantly less VSMC coverage compared with age-matched controls, measured along each artery as a percentage of the outgrowth of the vascular plexus (dotted lines). Arterial coverage is reduced 37% at P3, 21% at P5, and 17% at P7. Values represent means ± SEM. C57BL/6 (n = 12 [P3], n = 23 [P5], n = 19 [P7]), VWF KO (n = 14 [P3], n = 25 [P5], n = 14 [P7]), where n is the number of retinas analyzed. P = 9.3 × 10−4 (P3), P = 1.7 × 10−9 (P5), P = 7.3 × 10−3 (P7). Scale bars: 150 μm (P3), 300 μm (P5), and 600 μm (P7).

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