Department of Nephrology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China.
J Biol Chem. 2010 Dec 17;285(51):40019-27. doi: 10.1074/jbc.M110.141341. Epub 2010 Oct 21.
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.
Par-3 是 Par 复合物的一个组成部分,对紧密连接的完整性至关重要。我们之前的研究报道,TGF-β 下调大鼠近端肾小管上皮细胞中 Par-3 的表达,但潜在的机制尚不清楚。在本研究中,我们通过荧光素酶报告基因检测证实,miR-491-5p 通过 Par-3 3'UTR 上的结合位点下调荧光素酶活性。miR-491-5p 的过表达显著降低了内源性 Par-3 的表达,破坏了紧密连接,并导致跨上皮电阻降低。此外,miR-491-5p 的表达可被 TGF-β1 通过 MEK/p38 MAPK 通路诱导。重要的是,在梗阻性肾病大鼠模型中,miR-491-5p 的水平显著升高,与 Par-3 水平降低呈平行关系。总之,我们的研究表明,miR-491-5p 的上调有助于 TGF-β 调节 Par-3 的表达。我们的研究揭示了 TGF-β 破坏细胞连接的一种新机制。