A microRNA circuit mediates transforming growth factor-beta 1 autoregulation in renal glomerular mesangial cells

作者：Kato Mitsuo^*; Arce Laura; Wang Mei; Putta Sumanth; Lanting Linda; Natarajan Rama

来源：Kidney International, 2011, 80(4): 358-368.

DOI：10.1038/ki.2011.43

• cell signaling
• diabetic nephropathy
• fibrosis
• gene expression
• TGF-beta

Enhanced transforming growth factor-beta 1 (TGF-beta 1) expression in renal cells promotes fibrosis and hypertrophy during the progression of diabetic nephropathy. The TGF-beta 1 promoter is positively controlled by the E-box regulators, upstream stimulatory factors (USFs), in response to diabetic (high glucose) conditions; however, it is not clear whether TGF-beta 1 is autoregulated by itself. As changes in microRNAs (miRNAs) have been implicated in kidney disease, we tested their involvement in this process. TGF-beta 1 levels were found to be upregulated by microRNA-192 (miR-192) or miR-200b/c in mouse mesangial cells. Amounts of miR-200b/c were increased in glomeruli from type 1 (streptozotocin) and type 2 (db/db) diabetic mice, and in mouse mesangial cells treated with TGF-beta 1 in vitro. Levels of miR-200b/c were also upregulated by miR-192 in the mesangial cells, suggesting that miR-200b/c are downstream of miR-192. Activity of the TGF-beta 1 promoter was upregulated by TGF-beta 1 or miR-192, demonstrating that the miR-192-miR-200 cascade induces TGF-beta 1 expression. TGF-beta 1 increased the occupancy of activators USF1 and Tfe3, and decreased that of the repressor Zeb1 on the TGF-beta 1 promoter E-box binding sites. Inhibitors of miR-192 decreased the expression of miR-200b/c, Col1a2, Col4a1, and TGF-beta 1 in mouse mesangial cells, and in mouse kidney cortex. Thus, miRNA-regulated circuits may amplify TGF-beta 1 signaling, accelerating chronic fibrotic diseases such as diabetic nephropathy. Kidney International (2011) 80, 358-368; doi:10.1038/ki.2011.43; published online 9 March 2011

• 出版日期2011-8