Loss of GCN5L1 in cardiac cells limits mitochondrial respiratory capacity under hyperglycemic conditions

Physiol Rep. 2019 Apr;7(8):e14054. doi: 10.14814/phy2.14054.

Abstract

The mitochondrial acetyltransferase-related protein GCN5L1 controls the activity of fuel substrate metabolism enzymes in several tissues. While previous studies have demonstrated that GCN5L1 regulates fatty acid oxidation in the prediabetic heart, our understanding of its role in overt diabetes is not fully developed. In this study, we examined how hyperglycemic conditions regulate GCN5L1 expression in cardiac tissues, and modeled the subsequent effect in cardiac cells in vitro. We show that GCN5L1 abundance is significantly reduced under diabetic conditions in vivo, which correlated with reduced acetylation of known GCN5L1 fuel metabolism substrate enzymes. Treatment of cardiac cells with high glucose reduced Gcn5l1 expression in vitro, while expression of the counteracting deacetylase enzyme, Sirt3, was unchanged. Finally, we show that genetic depletion of GCN5L1 in H9c2 cells leads to reduced mitochondrial oxidative capacity under high glucose conditions. These data suggest that GCN5L1 expression is highly responsive to changes in cellular glucose levels, and that loss of GCN5L1 activity under hyperglycemic conditions impairs cardiac energy metabolism.

Keywords: GCN5L1; SIRT3; bioenergetics; hyperglycemia; mitochondria; respiration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetyltransferases / genetics*
  • Acetyltransferases / metabolism
  • Animals
  • Cell Line
  • Cell Respiration
  • Energy Metabolism*
  • Glucose / metabolism
  • Hyperglycemia / metabolism*
  • Male
  • Mitochondria, Heart / metabolism*
  • Mitochondrial Proteins / genetics*
  • Mitochondrial Proteins / metabolism
  • Oxidative Stress
  • Rats
  • Rats, Zucker
  • Sirtuins / genetics
  • Sirtuins / metabolism

Substances

  • GCN5L1 protein, rat
  • Mitochondrial Proteins
  • SIRT3 protein, rat
  • Acetyltransferases
  • Sirtuins
  • Glucose