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Autophagy is involved in aldosterone-induced mesangial cell proliferation

机译:自噬参与醛固酮诱导的系膜细胞增殖

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摘要

The aim of the present study was to investigate whether autophagy is involved in aldosterone (Aldo)-induced mesangial cell (MC) proliferation. MCs were incubated with 10−7 M Aldo for 24 h. Proliferation of MCs, and the underlying mechanisms, were subsequently analyzed using [3H]thymidine assay, cell counting assay, western blotting and RNA interference (RNAi). Aldo was revealed to induce autophagy, as indicated by the increased conversion from microtubule-associated protein 1A/1B-light chain 3 (LC3)-I to LC3-II, the increased expression levels of autophagy-related gene 7 (Atg7) and the increased degradation of p62, which was accompanied by MC proliferation. Notably, pharmacological inhibition of autophagy or RNAi-mediated knockdown of Atg7 attenuated Aldo-induced MC proliferation, suggesting that autophagy was at least partially responsible for this effect. The results of the present study provided evidence that autophagy is critical for regulating Aldo-induced MC proliferation.
机译:本研究的目的是研究自噬是否与醛固酮(Aldo)诱导的系膜细胞(MC)增殖有关。 MCs与10 -7 M Aldo一起孵育24小时。随后使用[ 3 H]胸苷测定,细胞计数测定,蛋白质印迹和RNA干扰(RNAi)分析MC的增殖及其潜在机制。从微管相关蛋白1A / 1B-轻链3(LC3)-I到LC3-II的转化增加,自噬相关基因7(Atg7)的表达水平增加表明,Aldo可以诱导自噬。增加p62的降解,并伴随MC增殖。值得注意的是,药理学抑制自噬或Ati7的RNAi介导的敲低减弱了Aldo诱导的MC增殖,表明自噬至少部分负责这种作用。本研究的结果提供证据表明自噬对调节Aldo诱导的MC增殖至关重要。

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