Par-3 is a component of Par complex, which is critical for the integrity of tight junction. We previously reported that TGF-β down-regulated Par-3 expression in rat proximal tubular epithelial cells, but the underlying mechanism remains unknown. In the present study, we demonstrated by a luciferase reporter assay that miR-491-5p down-regulated the luciferase activity through a binding site in the 3' UTR of Par-3. Overexpression of miR-491-5p dramatically decreased the expression of endogenous Par-3, disrupted tight junction, and resulted in decreased transepithelial resistance. Moreover, miR-491-5p expression was induced by TGF-β1 through the MEK/p38 MAPK pathway. Importantly, miR-491-5p levels were increased significantly in a rat model of obstructive nephropathy, in parallel with decreased Par-3 levels. Taken together, we conclude that up-regulation of miR-491-5p contributes to TGF-β-regulated Par-3 expression. Our study uncovered a novel mechanism by which TGF-β disrupts cell junction.
TGF-{beta}-induced MiR-491-5p expression promotes Par-3 degradation in rat proximal tubular epithelial cells.
TGF-β诱导的miR-491-5p表达促进大鼠近端肾小管上皮细胞中Par-3的降解
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作者:Zhou Qin, Fan Jinjin, Ding Xuebing, Peng Wenxing, Yu Xueqing, Chen Yueqin, Nie Jing
| 期刊: | Journal of Biological Chemistry | 影响因子: | 3.900 |
| 时间: | 2010 | 起止号: | 2010 Dec 17; 285(51):40019-27 |
| doi: | 10.1074/jbc.M110.141341 | 种属: | Rat |
| 研究方向: | 细胞生物学 | ||
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