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. 2013 Oct 31;2013:297537. doi: 10.1155/2013/297537

Figure 1.

Figure 1

Wild-type and Bim−/− cells morphology. Wild-type and Bim−/− retinal endothelial cells (panel (a)) and pericytes (panel (b)) were cultured on gelatin or uncoated plates, respectively. Cells were photographed using a phase microscope in digital format at low magnification (×40). In panel (c), retinal endothelial cells prepared from wild-type and Bim−/− mice were examined for the expression of PECAM-1 and VE-cadherin FACScan analysis. In panel (d), retinal pericytes from wild-type and Bim−/− mice were examined for the expression of NG2 and PDGFR-β by FACScan analysis. The shaded areas show staining in the presence of control IgG.