Figure 2
Figure 2. Loss of Endosialin results in increased vessel density. Retinas from littermate Endosialin+/+, Endosialin+/−, and Endosialin−/− C57BL/6 mice were stained with FITC–isolectin B4 and NG2 followed by Alexa Fluor 555–anti–rabbit Ig. (A) Low-power images of P4 retinas with box indicating the field of view in the central capillary plexus analyzed for quantification of vessel density in panels B and C. (B) Quantification of vessel density (Metamorph software tool)/100 μm2 ± SEM. (C) Quantification of vessel density (manual counting of branch points)/100 μm2 ± SEM. Endosialin+/+: P2, n = 5; P3, n = 7; P4, n = 5; P7, n = 3. Endosialin+/−: P2, n = 5; P3, n = 4; P4, n = 5; P7, n = 7. Endosialin−/−: P2, n = 4; P3, n = 4; P4, n = 5; P7, n = 5. (D) Confocal images of P4 retinas to illustrate no difference in NG2-positive pericyte coverage in Endosialin+/+, Endosialin+/−, and Endosialin−/− mice. a indicates arteries; and v, veins. Scale bar indicates 200 μm.

Loss of Endosialin results in increased vessel density. Retinas from littermate Endosialin+/+, Endosialin+/−, and Endosialin−/− C57BL/6 mice were stained with FITC–isolectin B4 and NG2 followed by Alexa Fluor 555–anti–rabbit Ig. (A) Low-power images of P4 retinas with box indicating the field of view in the central capillary plexus analyzed for quantification of vessel density in panels B and C. (B) Quantification of vessel density (Metamorph software tool)/100 μm2 ± SEM. (C) Quantification of vessel density (manual counting of branch points)/100 μm2 ± SEM. Endosialin+/+: P2, n = 5; P3, n = 7; P4, n = 5; P7, n = 3. Endosialin+/−: P2, n = 5; P3, n = 4; P4, n = 5; P7, n = 7. Endosialin−/−: P2, n = 4; P3, n = 4; P4, n = 5; P7, n = 5. (D) Confocal images of P4 retinas to illustrate no difference in NG2-positive pericyte coverage in Endosialin+/+, Endosialin+/−, and Endosialin−/− mice. a indicates arteries; and v, veins. Scale bar indicates 200 μm.

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