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Mitochondrial dysfunction resulting from loss of cytochrome c impairs cellular oxygen sensing and hypoxic HIF-alpha activation.

Authors
  • Mansfield, Kyle D
  • Guzy, Robert D
  • Pan, Yi
  • Young, Regina M
  • Cash, Timothy P
  • Schumacker, Paul T
  • Simon, M Celeste
Type
Published Article
Journal
Cell Metabolism
Publisher
Elsevier
Publication Date
Jun 01, 2005
Volume
1
Issue
6
Pages
393–399
Identifiers
PMID: 16054088
Source
Medline
License
Unknown

Abstract

While cellular responses to low oxygen (O(2)) or hypoxia have been studied extensively, the precise identity of mammalian cellular O(2) sensors remains controversial. Using murine embryonic cells lacking cytochrome c, and therefore mitochondrial activity, we show that mitochondrial reactive oxygen species (mtROS) are essential for proper O(2) sensing and subsequent HIF-1 alpha and HIF-2 alpha stabilization at 1.5% O(2). In the absence of this signal, HIF-alpha subunits continue to be degraded. Furthermore, exogenous treatment with H(2)O(2) or severe O(2) deprivation is sufficient to stabilize HIF-alpha even in the absence of cytochrome c and functional mitochondria. These results provide genetic evidence indicating that mtROS act upstream of prolyl hydroxylases in regulating HIF-1 alpha and HIF-2 alpha in this O(2)-sensing pathway.

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