A non-hypoxic, ROS-sensitive pathway mediates TNF-alpha-dependent regulation of HIF-1alpha

FEBS Lett. 2001 Sep 14;505(2):269-74. doi: 10.1016/s0014-5793(01)02833-2.

Abstract

A non-hypoxic, reactive oxygen species (ROS)-sensitive pathway mediating tumor necrosis factor-alpha (TNF-alpha)-dependent regulation of hypoxia-inducible factor-1alpha (HIF-alpha) was investigated in vitro. TNF-alpha mediated the translocation of HIF-1alpha, associated with up-regulating its activity under normoxia. Analysis of the mode of action of TNF-alpha revealed the accumulation of hydrogen peroxide (H2O2), superoxide anion (O(2-.)) and hydroxyl radical (.OH). Antioxidants purported as prototypical scavengers of H2O2 and .OH, attenuated TNF-alpha-induced HIF-1alpha activation, and blockading NADPH-oxidase by scavenging O(2-.) reduced the activity of HIF-1alpha. Inhibition of the mitochondrion complex I abrogated TNF-alpha-dependent activation of HIF-1alpha. Interrupting the respiratory chain reversed the excitatory effect of TNF-alpha on HIF-1alpha. These results indicate a non-hypoxic pathway mediating cytokine-dependent regulation of HIF-1alpha in a ROS-sensitive mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anions
  • Antioxidants / pharmacology
  • Apoptosis
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • DNA / metabolism
  • DNA-Binding Proteins / metabolism*
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • Fibroblasts / metabolism
  • Hydrogen Peroxide / pharmacology
  • Hypoxia
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Inflammation
  • Inhibitory Concentration 50
  • Mice
  • Mitochondria / metabolism
  • Nuclear Proteins / metabolism*
  • Protein Transport
  • Reactive Oxygen Species / metabolism*
  • Recombinant Proteins / metabolism
  • Time Factors
  • Transcription Factors*
  • Tumor Necrosis Factor-alpha / metabolism*
  • Up-Regulation

Substances

  • Anions
  • Antioxidants
  • DNA-Binding Proteins
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Nuclear Proteins
  • Reactive Oxygen Species
  • Recombinant Proteins
  • Transcription Factors
  • Tumor Necrosis Factor-alpha
  • DNA
  • Hydrogen Peroxide