MiR-30c protects diabetic nephropathy by suppressing epithelial-to-mesenchymal transition in db/db mice

Aging Cell. 2017 Apr;16(2):387-400. doi: 10.1111/acel.12563. Epub 2017 Jan 27.

Abstract

Epithelial-to-mesenchymal transition (EMT) plays a significant role in tubulointerstitial fibrosis, which is a hallmark of diabetic nephropathy. Thus, identifying the mechanisms of EMT activation could be meaningful. In this study, loss of miR-30c accompanied with increased EMT was observed in renal tubules of db/db mice and cultured HK2 cells exposed to high glucose. To further explore the roles of miR-30c in EMT and tubulointerstitial fibrosis, recombinant adeno-associated viral vector was applied to manipulate the expression of miR-30c. In vivo study showed that overexpression of miR-30c suppressed EMT, attenuated renal tubulointerstitial fibrosis and reduced proteinuria, serum creatinine, and BUN levels. In addition, Snail1 was identified as a direct target of miR-30c by Ago2 co-immunoprecipitation, luciferase reporter, and Western blot assays. Downregulating Snail1 by siRNA reduced high glucose-induced EMT in HK2 cells, and miR-30c mimicked the effects. Moreover, miR-30c inhibited Snail1-TGF-β1 axis in tubular epithelial cells undergoing EMT and thereby impeded the release of TGF-β1; oppositely, knockdown of miR-30c enhanced the secretion of TGF-β1 from epitheliums and significantly promoted proliferation of fibroblasts and fibrogenesis of myofibroblasts, aggravated tubulointerstitial fibrosis, and dysfunction of diabetic nephropathy. These results suggest a protective role of miR-30c against diabetic nephropathy by suppressing EMT via inhibiting Snail1-TGF-β1 pathway.

Keywords: Snail1; TGF-β1; diabetic nephropathy; epithelial-to-mesenchymal transition; miR-30c.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Diabetic Nephropathies / genetics*
  • Diabetic Nephropathies / pathology*
  • Down-Regulation / drug effects
  • Down-Regulation / genetics*
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Epithelial-Mesenchymal Transition* / drug effects
  • Glucose / toxicity
  • HEK293 Cells
  • Humans
  • Kidney Tubules / drug effects
  • Kidney Tubules / pathology
  • Kidney Tubules / physiopathology
  • Mice, Inbred C57BL
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Protective Agents / metabolism*
  • Snail Family Transcription Factors / metabolism
  • Transforming Growth Factor beta1 / metabolism

Substances

  • MicroRNAs
  • Mirn30d microRNA, mouse
  • Protective Agents
  • Snail Family Transcription Factors
  • Transforming Growth Factor beta1
  • Glucose