标题:Downregulation of MiR-218 can alleviate high-glucose-induced renal proximal tubule injury by targeting GPRC5A
作者:Su, Shan-Shan; Li, Bao-Peng; Li, Chun-Lin; Xiu, Fang-Rui; Wang, Dong-Yan; Zhang, Fa-Rong
作者机构:[Su, Shan-Shan] Shandong Univ Tradit Chinese Med, Jinan, Peoples R China.; [Su, Shan-Shan; Xiu, Fang-Rui; Wang, Dong-Yan; Zhang, Fa-Rong] Shandong U 更多
通讯作者:Zhang, FR
通讯作者地址:[Zhang, FR]Shandong Univ Tradit Chinese Med, Dept Nephrol, Affiliated Hosp, Jinan, Peoples R China.
来源:BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
DOI:10.1080/09168451.2020.1717330
关键词:miR-218; GPRC5a; diabetic nephropathy; target; high-glucose
摘要:The purpose of this study was to explore the functional implication of microRNA-218 (miR-218) in diabetic nephropathy (DN) through high-glucose-stimulated renal proximal tubule impairment. Biological function experiments showed that miR-218 and inflammatory factors TNF-alpha and IL-1 beta were highly expressed in renal proximal tubule under high-glucose conditions. Inhibiting miR-218 alleviated renal tubular cell injury, which was represented by miR-218 inhibitor facilitating renal tubular cell vitality whilst reducing its apoptosis and levels of inflammation factors. In addition, we confirmed that miR-218 directly targeted GPRC5A and negatively regulated its expression. Co-transfection assay showed that overexpression of GPRC5A accentuated the mitigated action of miR-218 inhibitor on renal proximal tubule cell injury induced by high-glucose. Accordingly, these data indicated that downregulation of miR-218 can assuage high-glucose-resulted renal tubular cell damage, and its ameliorative effect was achieved by negative regulation of GPRC5A, which provides a novel direction for unearthing the pathogenesis and even further biological treatment of DN.
收录类别:SCIE
资源类型:期刊论文
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