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首页> 外文期刊>Chinese Medical Journal >Caspase-3 and its inhibitor Ac-DEVD-CHO in rat lens epithelial cell apoptosis induced by hydrogen in vitro
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Caspase-3 and its inhibitor Ac-DEVD-CHO in rat lens epithelial cell apoptosis induced by hydrogen in vitro

机译:Caspase-3及其抑制剂Ac-DEVD-CHO在体外氢致大鼠晶状体上皮细胞凋亡中的作用

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摘要

Objective To investigate the role of caspase-3 and its inhibitor Ac-DEVD-CHO in rat lens epithelial cell apoptosis induced by hydrogen peroxide (H_2O_2) in vitro. Methods Rat lenses were incubated in modified Eagle's medium containing 2 mmol/L H_2O_2 to induce apoptosis in vitro. Apoptosis in lens epithelial cells was assessed by transmission electron microscopy and annexin V-propidium iodide (PI) double staining flow cytometry after 12, 24 and 48 h of incubation. The activity of caspase-3 was analyzed by western blotting. Results Observations under transmission electron microscopy revealed that 2 mmol/L H_2O_2 could effectively induce lens epithelial cell apoptosis in vitro. Caspase-3 activity increased during cell apoptosis and the peak measurement occurred at 24 h after treatment with H_2O_2. Cell apoptosis was blocked by caspase-3 inhibitor Ac-DEVD-CHO. Conclusions The activation of caspase-3 plays an important role in executing apoptosis in H_2O_2-treated lens epithelial cells and in the formation of cataract. The caspase-3 inhibitor Ac-DEVD-CHO may effectively prevent lens epithelial cell apoptosis caused by oxidative injury.
机译:目的探讨caspase-3及其抑制剂Ac-DEVD-CHO在过氧化氢(H_2O_2)诱导的大鼠晶状体上皮细胞凋亡中的作用。方法将大鼠晶状体在含有2 mmol / L H_2O_2的改良Eagle培养基中孵育,以诱导细胞凋亡。培养12、24和48小时后,通过透射电子显微镜和膜联蛋白V-碘化丙啶(PI)双染色流式细胞术评估晶状体上皮细胞的凋亡。通过蛋白质印迹分析了caspase-3的活性。结果透射电镜观察发现2 mmol / L H_2O_2可以有效诱导晶状体上皮细胞凋亡。 Caspase-3活性在细胞凋亡过程中增加,并且在H_2O_2处理后24小时达到峰值。细胞凋亡被caspase-3抑制剂Ac-DEVD-CHO阻断。结论caspase-3的激活在H_2O_2处理的晶状体上皮细胞凋亡和白内障形成中起重要作用。 caspase-3抑制剂Ac-DEVD-CHO可有效防止氧化损伤引起的晶状体上皮细胞凋亡。

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