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[摘要]：Transforming growth factor-beta 1 (TGF-beta 1)-induced epithelial-to-mesenchymal transition (EMT) contributes to the pathophysiological development of kidney fibrosis. Although it was reported that TGF-beta 1 enhances beta(1) integrin levels in NMuMG cells, the detailed molecular mechanisms underlying TGF-beta 1-induced beta(1) integrin gene expression and the role of beta(1) integrin during EMT in the renal system are still unclear. In this study, we examined the role of beta(1) integrin in TGF-beta 1-induced EMT both in vitro and in vivo. TGF-beta 1-induced augmentation of beta(1) integrin expression was required for EMT in several epithelial cell lines, and knockdown of Smad3 inhibited TGF-beta 1-induced augmentation of beta(1) integrin. TGF-beta 1 triggered beta(1) integrin gene promoter activity as assessed by luciferase activity assay. Both knockdown of Smad3 and mutation of the Smad-binding element to block binding to the beta(1) integrin promoter markedly reduced TGF-beta 1-induced beta(1) integrin promoter activity. Chromatin immunoprecipitation assay showed that TGF-beta 1 enhanced Smad3 binding to the beta(1) integrin promoter. Furthermore, induction of unilateral ureteral obstruction triggered increases of beta(1), integrin in both renal epithelial and interstitial cells. In human kidney with chronic tubulointerstitial fibrosis, we also found a concomitant increase of beta(1), integrin and a-smooth muscle actin in tubule epithelia. Blockade of beta(1) integrin signaling dampened the progression of fibrosis. Taken together, beta(1) integrin mediates EMT and subsequent tubulointerstitutial fibrosis, suggesting that inhibition of beta(1), integrin is a possible therapeutic target for prevention of renal fibrosis. (Am J Pathol 2010, 177:1743-1754; DOI: 10.2353/ajpath.2010.091183) |
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