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TWIK-related acid-sensitive K(+) channel 2 promotes renal fibrosis by inducing cell-cycle arrest

TWIK-related acid-sensitive K(+) channel-2 (TASK-2, encoded by Kcnk5) is essential in cell biological processes, by regulating transmembrane K(+) balance. In the present study, we aimed to clarify the role of TASK-2 in renal fibrosis and explore the underlying mechanism. We found that TASK-2 level w...

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Detalles Bibliográficos
Autores principales: Zhang, Jian, Chen, Jing, Lu, Yufei, Yang, Yan, Chen, Weize, Shen, Bo, Hu, Jiachang, Jia, Ping, Xu, Sujuan, Shi, Yiqin, Ning, Yichun, Wang, Jialin, Fang, Yi, Zhao, Shuan, Li, Yang, Dai, Yan, Zhang, Xiaoyan, Xiang, Meng, Tian, Yang, Liu, Zhichao, Song, Nana, Ding, Xiaoqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9712759/
https://www.ncbi.nlm.nih.gov/pubmed/36465115
http://dx.doi.org/10.1016/j.isci.2022.105620
Descripción
Sumario:TWIK-related acid-sensitive K(+) channel-2 (TASK-2, encoded by Kcnk5) is essential in cell biological processes, by regulating transmembrane K(+) balance. In the present study, we aimed to clarify the role of TASK-2 in renal fibrosis and explore the underlying mechanism. We found that TASK-2 level was elevated in the renal tubular UUO- and UIR-induced renal fibrosis as well as in patients with renal tubulointerstitial fibrosis. Knockout of Kcnk5 or inhibition of TASK-2 in renal tubules attenuated G2/M cell-cycle arrest and alleviated renal fibrosis. Mechanistically, demethylase fat mass and obesity-associated protein (FTO) reduced N6-adenosine methylation (m6A) of Kcnk5 mRNA following renal fibrosis. FTO deficiency attenuated the upregulation of TASK-2 and renal fibrosis. The results demonstrated the crucial role of TASK-2 in renal fibrosis, which is conducive to a better understanding of the pathogenesis of renal fibrosis. TASK-2 may be a potential treatment strategy to alleviate the development of renal fibrosis.