Glutathione peroxidase-1 regulates mitochondrial function to modulate redox-dependent cellular responses

J Biol Chem. 2009 May 1;284(18):11913-21. doi: 10.1074/jbc.M900392200. Epub 2009 Mar 2.

Abstract

Glutathione peroxidase-1 (GPx-1) is a selenocysteine-containing enzyme that plays a major role in the reductive detoxification of peroxides in cells. In permanently transfected cells with approximate 2-fold overexpression of GPx-1, we found that intracellular accumulation of oxidants in response to exogenous hydrogen peroxide was diminished, as was epidermal growth factor receptor (EGFR)-mediated Akt activation in response to hydrogen peroxide or EGF stimulation. Knockdown of GPx-1 augmented EGFR-mediated Akt activation, whereas overexpression of catalase decreased Akt activation, suggesting that EGFR signaling is regulated by redox mechanisms. To determine whether mitochondrial oxidants played a role in these processes, cells were pretreated with a mitochondrial uncoupler prior to EGF stimulation. Inhibition of mitochondrial function attenuated EGF-mediated activation of Akt in control cells but had no additional effect in GPx-1-overexpressing cells, suggesting that GPx-1 overexpression decreased EGFR signaling by decreasing mitochondrial oxidants. Consistent with this finding, GPx-1 overexpression decreased global protein disulfide bond formation, which is dependent on mitochondrially produced oxidants. GPx-1 overexpression, in permanently transfected or adenovirus-treated cells, also caused overall mitochondrial dysfunction with a decrease in mitochondrial potential and a decrease in ATP production. GPx-1 overexpression also decreased EGF- and serum-mediated [(3)H]thymidine incorporation, indicating that alterations in GPx-1 can attenuate cell proliferation. Taken together, these data suggest that GPx-1 can modulate redox-dependent cellular responses by regulating mitochondrial function.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / biosynthesis
  • Adenosine Triphosphate / genetics
  • Adenoviridae
  • Catalase / genetics
  • Catalase / metabolism
  • Cell Line
  • Cell Proliferation / drug effects
  • Disulfides / metabolism
  • Enzyme Activation / drug effects
  • Enzyme Activation / physiology
  • Epidermal Growth Factor / genetics
  • Epidermal Growth Factor / metabolism
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • Gene Knockdown Techniques
  • Glutathione Peroxidase / genetics
  • Glutathione Peroxidase / metabolism*
  • Glutathione Peroxidase GPX1
  • Humans
  • Hydrogen Peroxide / metabolism*
  • Hydrogen Peroxide / pharmacology
  • Mitochondria, Liver / genetics
  • Mitochondria, Liver / metabolism*
  • Oxidants / metabolism*
  • Oxidants / pharmacology
  • Oxidation-Reduction / drug effects
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Selenocysteine / genetics
  • Selenocysteine / metabolism
  • Selenoproteins / genetics
  • Selenoproteins / metabolism*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • Transduction, Genetic / methods
  • Uncoupling Agents / pharmacology

Substances

  • Disulfides
  • Oxidants
  • Selenoproteins
  • Uncoupling Agents
  • Selenocysteine
  • Epidermal Growth Factor
  • Adenosine Triphosphate
  • Hydrogen Peroxide
  • Catalase
  • Glutathione Peroxidase
  • EGFR protein, human
  • ErbB Receptors
  • Proto-Oncogene Proteins c-akt
  • Glutathione Peroxidase GPX1