SGK1 Attenuates Oxidative Stress-Induced Renal Tubular Epithelial Cell Injury by Regulating Mitochondrial Function

Figure 3

SGK1 knockdown increases H₂O₂-induced cell injury through the GSK3β pathway in HK-2 cells. HK-2 cells transfected with scramble control (null) or SGK1 shRNA (shRNA-SGK1) for 72 h were incubated with the GSK3β inhibitor SB216763 (SB21, 10 μM) for 1 h and then treated with H₂O₂ (250 μM) for 2 h. (a) Cell viability was assessed via the CCK-8 assay. (b) Cell apoptosis was determined by flow cytometric analysis with annexin-V/PI double-staining. (c–f) The expression levels of apoptosis-related proteins in HK-2 cells were detected by western blot analysis. Data are presented as the (). , , and .

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