The cellular basis for diverse responses to oxygen

Navdeep S. Chandel, G. R.Scott Budinger*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

191 Scopus citations

Abstract

Mammalian cells have divergent responses to varying oxygen levels. Cells exposed to low oxygen levels (hypoxia) activate the transcription factor hypoxia-inducible factor-1 (HIF-1) as an adaptive response. Cells exposed to hypoxia do not undergo senescence or cell death and do not diminish ATP levels. By contrast, cells exposed to high oxygen levels (hyperoxia) undergo senescence and cell death and decrease their ATP levels, yet do not activate HIF-1. Despite these divergent responses with respect to senescence, cell death, metabolism, and gene expression, the signaling events in both systems are mediated by the generation of mitochondrial-derived reactive oxygen species (ROS). This perspective reviews the role of signaling through mitochondrial ROS in hypoxic and hyperoxic environments.

Original languageEnglish (US)
Pages (from-to)165-174
Number of pages10
JournalFree Radical Biology and Medicine
Volume42
Issue number2
DOIs
StatePublished - Jan 15 2007

Keywords

  • AMPK
  • ATP
  • Aging
  • Apoptosis
  • Bcl-2 proteins
  • Electron transport
  • Free radicals
  • HIF
  • Hyperoxia
  • Hypoxia
  • Metabolism
  • Mitochondria
  • Reactive oxygen species
  • Senescence

ASJC Scopus subject areas

  • Biochemistry
  • Physiology (medical)

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