Department of Ophthalmology, Harbin Medical University, The 2nd Affiliated Hospital, Harbin, Heilongjiang, China (mainland).
Med Sci Monit Basic Res. 2020 Apr 27;26:e923391. doi: 10.12659/MSMBR.923391.
BACKGROUND The primary purpose of this study was to investigate the protective effect of metformin against hydrogen peroxide (H₂O₂)-induced cellular senescence and to explore the underlying molecular mechanism of lens epithelial cell senescence. MATERIAL AND METHODS We used H₂O₂ to establish senescence in human lens epithelial B3 cells. The cells were exposed to H₂O₂ for different numbers of days to mimic aging. Senescence was assessed by senescence-associated ß-galactosidase staining, and the molecular mechanism was assessed by real-time polymerase chain reaction (RT-PCR) and western blot analysis. The cultured cells were exposed to 150 μM H₂O₂ for 7 days with or without metformin to detect the underlying molecular mechanism of lens epithelial cell senescence. RESULTS The lens epithelial cells exposed to 150 µM H₂O₂ for 7 days exhibited senescence. The expression levels of senescence-related markers were increased in H₂O₂-treated cells. Metformin prevented H₂O₂-induced cellular senescence in human lens epithelial B3 cells. CONCLUSIONS These findings suggest that senescence marker expression is increased in the cells exposed to H₂O₂. Metformin protects human lens epithelial B3 cells from H₂O₂-induced senescence.
本研究的主要目的是探讨二甲双胍对过氧化氢(H₂O₂)诱导的细胞衰老的保护作用,并探讨晶状体上皮细胞衰老的潜在分子机制。
我们使用 H₂O₂ 来建立人晶状体上皮细胞 B3 细胞的衰老模型。将细胞暴露于 H₂O₂ 中不同天数以模拟衰老。通过衰老相关β-半乳糖苷酶染色评估衰老,通过实时聚合酶链反应(RT-PCR)和蛋白质印迹分析评估分子机制。用或不用二甲双胍将培养的细胞暴露于 150 μM H₂O₂ 7 天,以检测晶状体上皮细胞衰老的潜在分子机制。
暴露于 150 µM H₂O₂ 7 天的晶状体上皮细胞出现衰老。衰老相关标志物的表达水平在 H₂O₂ 处理的细胞中增加。二甲双胍可预防人晶状体上皮 B3 细胞的 H₂O₂ 诱导的细胞衰老。
这些发现表明,暴露于 H₂O₂ 的细胞中衰老标志物的表达增加。二甲双胍可保护人晶状体上皮 B3 细胞免受 H₂O₂ 诱导的衰老。