AIM: To evaluate the influence of hydrogen peroxide (H2O2) on mouse photoreceptor-derived 661W cell survival and to determine the effect of PD98059, an inhibitor for MEK1 (the direct upstream activator of ERK1/2), and S3I201, a STAT3- specific inhibitor on 661W cell survival after H2O2 exposure. · METHODS: The mouse photoreceptor-derived 661W cells were cultured. 661W cells were treated for 12 hours with different concentrations (0, 0.25, 0.50, 0.75, 1mmol/L) of H2O2 and cell viability was determined by 3-(4, 5-dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide)(MTT) assay. 661W cells were treated with different concentrations H2O2 (0, 5, 10, 50, 500, 1000 μmol/L) for 15 minutes or 1mmol/L H2O2 for different time points (0,5,10,15,30 minutes), and p-Tyr705-STAT3, STAT3, Phospho-p44/42 MAPK (Thr202/Tyr204), ERK1/2 were surveyed by immunoblot analysis. After treatment with 50μmol/L PD98059, or S3I201 for 1 hour, the inhibition efficiency of cell signal pathways was analyzed by immunoblot analysis and the effects of inhibitors on cell viability were determined by MTT. · RESULTS: After treating with different concentrations of H2O2 for 12 hours, the cell viability of 661W cells decreased in concentration-dependent manner (P<0.05). Moreover, H2O2 induced phosphorylation of ERK1/2 and STAT3 in 661W cells (P <0.05). After pretreatment with 50μmol/L PD98059 or S3I201 for 1 hour, H2O2-induced phosphorylation of ERK1/2 or STAT3 was suppressed separately (P<0.05). Using PD98059 or S3I201 to inhibit ERK1/2 or STAT3 signal pathway, the cell viability of 661W cells decreased significantly (P<0.05). · CONCLUSION: We demonstrated that the exposure of 661W cells to H2O2 increased the activation of ERK1/2 and STAT3 signal pathways. Activation of these pathways is required for 661W cell survival following oxidant injury. AIM: To evaluate the influence of hydrogen peroxide (H2O2) on mouse photoreceptor-derived 661W cell survival and determine the effect of PD98059, an inhibitor for MEK1 (the direct upstream activator of ERK1 / 2), and S3I201, a STAT3-specific inhibitor on 661W cell survival after H2O2 exposure. · METHODS: The mouse photoreceptor-derived 661W cells were cultured. 661W cells were treated for 12 hours with different concentrations (0, 0.25, 0.50, 0.75, 1 mmol / L) was determined by 3- (4,5-dimethylthiazolyl-2) -2,5-diphenyltetrazolium bromide (MTT) assay. 661W cells were treated with different concentrations of H2O2 (0,5, 10,50,50,100 μmol / L ) for 15 minutes or 1 mmol / L H2O2 for different time points (0,5,10,15,30 minutes), and p-Tyr705-STAT3, STAT3, Phospho- p44 / 42 MAPK (Thr202 / Tyr204) were surveyed by immunoblot analysis. After treatment with 50 μmol / L PD98059, or S3I201 for 1 hour, the inhibition efficiency of cell signal pathways was analyzed by immun oblot analysis and the effects of inhibitors on cell viability were determined by MTT. RESULTS: After treating with different concentrations of H2O2 for 12 hours, the cell viability of 661 W cells decreased in concentration-dependent manner (P <0.05) induced phosphorylation of ERK1 / 2 and STAT3 in 661W cells (P <0.05). After pretreatment with 50 μmol / L PD98059 or S3I201 for 1 hour, H2O2-induced phosphorylation of ERK1 / 2 or STAT3 was suppressed separately We demonstrated that the exposure of 661W cells to H2O2 increased the activation of ERK1 / 2 and STAT3 signal (P <0.05) pathways. Activation of these pathways is required for 661W cell survival following oxidant injury.