Overexpression of peroxisome proliferator-activated receptor gamma coactivator-1alpha down-regulates GLUT4 mRNA in skeletal muscles

J Biol Chem. 2003 Aug 15;278(33):31385-90. doi: 10.1074/jbc.M304312200. Epub 2003 May 30.

Abstract

Exercise training increases mitochondria and GLUT4 in skeletal muscles. Recent studies indicate that an increased expression of the transcriptional coactivator peroxisome proliferator-activated receptor gamma coactivator 1alpha (PGC-1alpha) by exercise may promote mitochondrial biogenesis and fatty acid oxidation. To examine whether increased PGC-1alpha expression was also responsible for an increase of GLUT4 expression, transgenic mice that overexpress PGC-1alpha in skeletal muscles driven by a human alpha-skeletal actin promoter were made. PGC-1alpha was overexpresssed in skeletal muscles including type I and II fiber-rich muscles but not in the heart. With an increase of PGC-1alpha mRNA, type II fiber-rich muscles were redder, and genes of mitochondrial oxidative metabolism were up-regulated in skeletal muscles, whereas the expression of GLUT4 mRNA was unexpectedly down-regulated. In parallel with a decrease of GLUT4 mRNA, an impairment of glycemic control after intraperitoneal insulin administration was observed. Thus, an increase of PGC-1alpha plays a role in increasing mitochondrial biogenesis and fatty acid oxidation but not in increasing GLUT4 mRNA in skeletal muscles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Down-Regulation / physiology
  • Electron Transport / genetics
  • Energy Metabolism / physiology
  • Fatty Acids / metabolism
  • Gene Expression / physiology
  • Glucose / metabolism
  • Glucose Transporter Type 4
  • Humans
  • Insulin / metabolism
  • Mice
  • Mice, Transgenic
  • Monosaccharide Transport Proteins / genetics*
  • Muscle Proteins*
  • Muscle, Skeletal / metabolism*
  • Oxidation-Reduction
  • RNA, Messenger / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism*
  • Up-Regulation / physiology

Substances

  • Fatty Acids
  • Glucose Transporter Type 4
  • Insulin
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • RNA, Messenger
  • SLC2A4 protein, human
  • Slc2a4 protein, mouse
  • Transcription Factors
  • peroxisome-proliferator-activated receptor-gamma coactivator-1
  • Glucose