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. 2013 Jan 7;54(1):63–71. doi: 10.1167/iovs.12-10312

Figure 4. .

Figure 4. 

Upregulation of glucose transporters in Hfe−/− primary RPE cells. (A) Real-time PCR analysis showing mRNA levels of sodium-coupled glucose transporter SGLT1 and facilitative glucose transporters (GLUT1-4) in Hfe+/+ and Hfe−/− RPE cells from passage three or four. (B) Uptake of [3H]-3-O-methyl-D-glucose was measured in passage two, three, and four (P2, P3, and P4) in Hfe+/+ and Hfe−/− RPE cells. Uptake was measured for 2 minutes at 37°C in the absence of Na+ with 1 μCi/well of [3H] 3-O-methyl-D-glucose and 50-μM unlabeled glucose. NMDG chloride was used to substitute for NaCl in the uptake medium. (C) Na+-independent and Na+-dependent uptakes of [3H]-3-O-methyl-D-glucose were also measured in Hfe+/+ and Hfe−/− RPE cells (P2). *P < 0.05; **P < 0.01; ***P < 0.001.