Gene expression profiling in hearts of diabetic mice uncovers a potential role of estrogen-related receptor γ in diabetic cardiomyopathy

Mol Cell Endocrinol. 2016 Jul 15:430:77-88. doi: 10.1016/j.mce.2016.04.004. Epub 2016 Apr 7.

Abstract

Diabetic cardiomyopathy is characterized by an abnormal oxidative metabolism, but the underlying mechanisms remain to be defined. To uncover potential mechanisms involved in the pathophysiology of diabetic cardiomyopathy, we performed a gene expression profiling study in hearts of diabetic db/db mice. Diabetic hearts showed a gene expression pattern characterized by the up-regulation of genes involved in lipid oxidation, together with an abnormal expression of genes related to the cardiac contractile function. A screening for potential regulators of the genes differentially expressed in diabetic mice found that estrogen-related receptor γ (ERRγ) was increased in heart of db/db mice. Overexpression of ERRγ in cultured cardiomyocytes was sufficient to promote the expression of genes involved in lipid oxidation, increase palmitate oxidation and induce cardiomyocyte hypertrophy. Our findings strongly support a role for ERRγ in the metabolic alterations that underlie the development of diabetic cardiomyopathy.

Keywords: Diabetes; Estrogen-related receptors; Fatty acid oxidation; Lipid metabolism; Orphan nuclear receptor; Transcriptional regulation of gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiomegaly / genetics
  • Cardiomegaly / pathology
  • Diabetes Mellitus, Experimental / genetics*
  • Diabetes Mellitus, Experimental / pathology*
  • Diabetes Mellitus, Experimental / physiopathology
  • Diabetic Cardiomyopathies / diagnostic imaging
  • Diabetic Cardiomyopathies / genetics*
  • Diabetic Cardiomyopathies / pathology*
  • Diabetic Cardiomyopathies / physiopathology
  • Gene Expression Profiling*
  • Gene Expression Regulation
  • Gene Regulatory Networks
  • Lipid Metabolism / genetics
  • Male
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Myocytes, Cardiac / metabolism
  • PPAR alpha / metabolism
  • Promoter Regions, Genetic / genetics
  • Receptors, Estrogen / metabolism*

Substances

  • Esrrg protein, mouse
  • PPAR alpha
  • Receptors, Estrogen