IHG-1 increases mitochondrial fusion and bioenergetic function

Diabetes. 2014 Dec;63(12):4314-25. doi: 10.2337/db13-1256. Epub 2014 Jul 9.

Abstract

Induced in high glucose-1 (IHG-1) is a conserved mitochondrial protein associated with diabetic nephropathy (DN) that amplifies profibrotic transforming growth factor (TGF)-β1 signaling and increases mitochondrial biogenesis. Here we report that inhibition of endogenous IHG-1 expression results in reduced mitochondrial respiratory capacity, ATP production, and mitochondrial fusion. Conversely, overexpression of IHG-1 leads to increased mitochondrial fusion and also protects cells from reactive oxygen species-induced apoptosis. IHG-1 forms complexes with known mediators of mitochondrial fusion-mitofusins (Mfns) 1 and 2-and enhances the GTP-binding capacity of Mfn2, suggesting that IHG-1 acts as a guanine nucleotide exchange factor. IHG-1 must be localized to mitochondria to interact with Mfn1 and Mfn2, and this interaction is necessary for increased IHG-1-mediated mitochondrial fusion. Together, these findings indicate that IHG-1 is a novel regulator of both mitochondrial dynamics and bioenergetic function and contributes to cell survival following oxidant stress. We propose that in diabetic kidney disease increased IHG-1 expression protects cell viability and enhances the actions of TGF-β, leading to renal proximal tubule dedifferentiation, an important event in the pathogenesis of this devastating condition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / genetics
  • Cell Respiration / genetics
  • Cell Survival / genetics
  • Diabetic Nephropathies / metabolism*
  • Energy Metabolism / genetics*
  • Fibrosis / genetics
  • Fibrosis / metabolism
  • GTP Phosphohydrolases / metabolism
  • HeLa Cells
  • Humans
  • Mitochondria / metabolism*
  • Mitochondrial Dynamics / genetics*
  • Mitochondrial Membrane Transport Proteins / metabolism
  • Mitochondrial Proteins / metabolism
  • Oxidative Stress
  • Proteins / genetics*
  • Proteins / metabolism
  • Reactive Oxygen Species / metabolism
  • Signal Transduction
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Mitochondrial Membrane Transport Proteins
  • Mitochondrial Proteins
  • Proteins
  • Reactive Oxygen Species
  • THG1L protein, human
  • Transforming Growth Factor beta1
  • GTP Phosphohydrolases
  • MFN2 protein, human
  • Mfn1 protein, human