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. 2020 Mar 8;26:188–203.

Figure 2.

Figure 2

OPN protein in cultured RPE cells. A: Cell cultures were immunolabeled with an antibody against OPN (red). The cell nuclei were stained with 4’,6-diamidino-2-phenylindole (DAPI; blue). The cells were cultured for 24 h under unstimulated control conditions and in the presence of high (+ 100 mM) NaCl and the hypoxia mimetic CoCl2 (150 µM), respectively. B: Double-immunolabeling of OPN (red) and cytokeratin (green). C: OPN secretion from RPE cells. The OPN protein level was determined with enzyme-linked immunosorbent assay (ELISA) in the media of cells cultured for 24 h in the presence of high (+ 100 mM) NaCl, sucrose (200 mM), and CoCl2 (150 µM). The data are expressed as percent of unstimulated control (100%). The numbers of independent experiments using cell lines from different donors are indicated in the bars. Statistically significant difference versus unstimulated control: *p<0.05. Scale bars in A and B, 20 µm.