A reducing environment stabilizes HIF-2alpha in SH-SY5Y cells under hypoxic conditions

FEBS Lett. 2008 Nov 26;582(28):3899-902. doi: 10.1016/j.febslet.2008.10.031. Epub 2008 Oct 26.

Abstract

Accumulating evidence suggests that hypoxia-inducible factor-2 (HIF-2) is important for the cellular response to hypoxia. However, it is not clear how HIF-2 is regulated under hypoxic conditions. We investigated kinetic changes in redox status and HIF-2alpha accumulation in hypoxic SH-SY5Y cells. Our results demonstrated that hypoxia caused a reducing environment and increased HIF-2alpha protein levels. Experiments with redox modulations (N-acetylcysteine and l-buthionine sulfoximine) confirmed that a reducing environment induced HIF-2alpha accumulation while an oxidizing environment decreased it. In addition, experiments with SOD mimic, catalase, and exogenous H2O2 provided evidence that the presence of H2O2 down-regulated the amount of HIF-2alpha protein. This study offers novel evidence supporting redox status regulation of HIF-2alpha accumulation under hypoxic conditions.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetylcysteine / pharmacology
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Buthionine Sulfoximine / pharmacology
  • Catalase / pharmacology
  • Cell Hypoxia / drug effects
  • Cell Line, Tumor
  • Free Radical Scavengers / pharmacology
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Oxidation-Reduction / drug effects
  • Superoxide Dismutase / pharmacology
  • Superoxide Dismutase-1

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Free Radical Scavengers
  • SOD1 protein, human
  • endothelial PAS domain-containing protein 1
  • Buthionine Sulfoximine
  • Hydrogen Peroxide
  • Catalase
  • Superoxide Dismutase
  • Superoxide Dismutase-1
  • Acetylcysteine