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Autophagy is involved in aldosterone-induced mesangial cell proliferation

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 [(3)H]thymidine assay,...

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Detalles Bibliográficos
Autores principales: Yang, Min, Wang, Bin, Miao, Liying, Xu, Xianlin, He, Xiaozhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102028/
https://www.ncbi.nlm.nih.gov/pubmed/27748808
http://dx.doi.org/10.3892/mmr.2016.5807
Descripción
Sumario: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 [(3)H]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.