MicroRNA-dependent regulation of KLF4 by glucose in vascular smooth muscle

J Cell Physiol. 2018 Sep;233(9):7195-7205. doi: 10.1002/jcp.26549. Epub 2018 Mar 25.

Abstract

Diabetes is a major risk factor for cardiovascular disease and this is in part due to the effects of hyperglycemia on vascular smooth muscle cells. Small non-coding microRNAs are known to control smooth muscle phenotype and arterial contractility and are dysregulated in diabetes. The effect of microRNAs on smooth muscle differentiation is in part mediated by the transcription factor KLF4 but the role of this mechanism in diabetic vascular disease is not fully understood. Herein, we have investigated the importance of hyperglycemia and diabetes for the expression of KLF4 in vascular smooth muscle and the involvement of miRNAs in this regulation. Hyperglycemia down-regulated KLF4 in vascular smooth muscle cells and similar results were found in arteries of diabetic mice and patients. This correlated with a Foxa2-dependent up-regulation of miR-29c, which targeted KLF4 in vascular smooth muscle cells. Importantly, by preventing downregulation of KLF4, the induction of smooth muscle contractile protein markers by glucose was inhibited. In conclusion, miR-29 mediated inhibition of KLF4 in hyperglycemic conditions contributes to increased expression of contractile markers in vascular smooth muscle cells. Further studies are warranted to determine the therapeutic implications of miR-29 inhibition in diabetic vascular disease.

Keywords: contractile differentiation; glucose; microRNA; vascular smooth muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • Biomarkers / metabolism
  • Diabetes Mellitus / genetics
  • Diabetes Mellitus / pathology
  • Gene Expression Regulation / drug effects*
  • Glucose / pharmacology*
  • Hepatocyte Nuclear Factor 3-beta / metabolism
  • Humans
  • Hyperglycemia / genetics
  • Hyperglycemia / pathology
  • Kruppel-Like Factor 4
  • Kruppel-Like Transcription Factors / genetics*
  • Kruppel-Like Transcription Factors / metabolism
  • Mice, Inbred C57BL
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Muscle Contraction / drug effects
  • Muscle, Smooth, Vascular / metabolism*
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • Biomarkers
  • KLF4 protein, human
  • Klf4 protein, mouse
  • Kruppel-Like Factor 4
  • Kruppel-Like Transcription Factors
  • MicroRNAs
  • RNA, Messenger
  • Hepatocyte Nuclear Factor 3-beta
  • Glucose