Activation of FoxO1/ PGC-1α prevents mitochondrial dysfunction and ameliorates mesangial cell injury in diabetic rats

Mol Cell Endocrinol. 2015 Sep 15:413:1-12. doi: 10.1016/j.mce.2015.06.007. Epub 2015 Jun 27.

Abstract

The generation of hyperglycemia-induced mitochondrial reactive oxygen species (ROS) is a key event in diabetic nephropathy development. The forkhead-box class O1 (FoxO1) and peroxisome proliferator-activated receptor γ co-activator 1α (PGC-1α) proteins are implicated in oxidative stress. We investigated the in vivo association of FoxO1 and PGC-1α in renal cortices from streptozotocin-induced diabetic rats and in rat kidney mesangial cells (MCs) treated with high glucose, in vitro. High-glucose induced FoxO1 inhibition was associated with decreased PGC-1α expression in MCs. These changes were accompanied by mitochondrial dysfunction and increased ROS generation. However, constitutive FoxO1 activation increased PGC-1α expression and partially reversed these changes, which were significantly decreased by the treatment of PGC-1α-small interfering RNA. We identified PGC-1α as a direct FoxO1 transcriptional target by chromatin immunoprecipitation. In addition, lentiviral-mediated FoxO1 overexpression in diabetic-rat kidneys significantly increased PGC-1α, NRF-1, and Mfn2 expression, and decreased malondialdehyde production and proteinuria. These data suggest that FoxO1/PGC-1α activation protected rats against high-glucose-induced MC injury by attenuating mitochondrial dysfunction and cellular ROS production.

Keywords: Diabetic nephropathy; Forkhead box class O1; Oxidative stress; Peroxisome proliferator-activated receptor γ co-activator 1α.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diabetes Mellitus, Experimental / genetics
  • Diabetes Mellitus, Experimental / metabolism*
  • Diabetes Mellitus, Experimental / pathology
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism*
  • GTP Phosphohydrolases
  • Gene Expression Regulation*
  • Glucose / metabolism
  • Male
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / genetics
  • Mesangial Cells / metabolism*
  • Mesangial Cells / pathology
  • Mitochondria / metabolism*
  • Mitochondria / pathology
  • Mitochondrial Proteins / biosynthesis
  • Mitochondrial Proteins / genetics
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Rats
  • Rats, Sprague-Dawley
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics

Substances

  • Forkhead Transcription Factors
  • Membrane Proteins
  • Mitochondrial Proteins
  • Nerve Tissue Proteins
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Ppargc1a protein, rat
  • Transcription Factors
  • Foxo1 protein, rat
  • GTP Phosphohydrolases
  • Mfn2 protein, rat
  • Glucose