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miRNA-34a inhibits cell adhesion by targeting CD44 in human renal epithelial cells: implications for renal stone disease.
Wang, Bohan; He, Gaofei; Xu, Gang; Wen, Jiaming; Yu, Xiao.
Affiliation
  • Wang B; Department of Urology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang University, Hangzhou, China.
  • He G; Department of Urology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang University, Hangzhou, China.
  • Xu G; Department of Urology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang University, Hangzhou, China.
  • Wen J; Department of Urology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang University, Hangzhou, China. wenjiaming@zju.edu.cn.
  • Yu X; Department of Urology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China. yujiuhu8366@126.com.
Urolithiasis ; 48(2): 109-116, 2020 Apr.
Article in En | MEDLINE | ID: mdl-31506763
ABSTRACT
Nephrolithiasis is a very common disease in which cell-crystal adhesion is an essential mechanism for kidney stone formation. This study has explored the anti-adhesion function of the microRNA, miR-34a, by targeting CD44, a cell surface receptor, in human renal epithelial (HK-2) cells. The expression of CD44 was monitored by qPCR and western blot. A luciferase assay validated the target of miR-34a in CD44 3' UTR. Immunofluorescence staining under confocal microscopy was used to detect the cell-crystal adhesion effects in vitro. Pizzolato staining was performed to examine the adhesion role of miR-34a in vivo. In HK-2 cells, miR-34a was down-regulated and CD44 was up-regulated when exposed to calcium oxalate monohydrate crystals. Moreover, miR-34a negatively regulated the expression of CD44. According to the luciferase report assay, miR-34a direct targeted a binding site in the CD44 3'UTR. In vitro experiments, miR-34a overexpression inhibited CD44 expression and cell-crystals adhesion; whereas CD44 overexpression showed reversed results. Furthermore, miR-34a suppressed cell-crystals adhesion and stone formation in vivo. These findings indicate that miR-34a targets CD44 in HK-2 cells and inhibits cell-crystal adhesion both in vitro and in vivo. Based on these results, miR-34a may be a potential therapeutic target for renal stone disease.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kidney Calculi / Cell Adhesion / Hyaluronan Receptors / MicroRNAs / Epithelial Cells Limits: Humans Language: En Journal: Urolithiasis Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kidney Calculi / Cell Adhesion / Hyaluronan Receptors / MicroRNAs / Epithelial Cells Limits: Humans Language: En Journal: Urolithiasis Year: 2020 Document type: Article Affiliation country: