Oxidative stress increases IL-8 production by RPE. ARPE-19 cells
were cultured in serum-, pyruvate-, and phenol red-free DMEM in the presence
of different concentrations of H2O2 for 1 h (panel
A), or in the presence of different concentrations of paraquat for 1 h
(panel B) and allowed to recover for 8 h in DMEM containing 10% FBS,
pyruvate, and phenol red. Alternatively, ARPE-19 cells were treated with blue
light, A2E, or A2E plus blue light as indicated under “Experimental
Procedures” (panel C). Levels of IL-8 in the medium were
detected by ELISA and expressed as -fold changes in response to oxidative
stress. The results are the mean ± S.D. of three independent
experiments. *, p < 0.01 as compared with the control group; #,
p < 0.01 as compared with blue light or A2E alone.