Journal
HYPOXIA AND CONSEQUENCES FROM MOLECULE TO MALADY
Volume 1177, Issue -, Pages 48-56Publisher
BLACKWELL PUBLISHING
DOI: 10.1111/j.1749-6632.2009.05046.x
Keywords
mitochondria; hypoxia; free radicals
Funding
- National Institutes of Health [GM30228]
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM030228] Funding Source: NIH RePORTER
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Eukaryotic cells respond to low oxygen concentrations by upregulating hypoxic and downregulating aerobic nuclear genes (hypoxic signaling). Most of the oxygen-regulated genes in yeast require the mitochondrial respiratory chain for their up- or downregulation when cells experience hypoxia. Although it was shown previously that the mitochondrial respiratory chain is required for the upregulation of some hypoxic genes in both yeast and mammalian cells, its underlying role in this process has been unclear. Recently, we have reported that mitochondria produce nitric oxide (NO center dot) when oxygen becomes limiting. This NO center dot production is nitrite (NO(2)(-))-dependent, requires an electron donor, and is carried out by cytochrome c oxidase in a pH-dependent fashion. We call this activity Cco/NO center dot and incorporate it into a new model for hypoxic signaling. In addition, we have found that some of the NO center dot produced by Cco/NO center dot is released from cells, raising the possibility that mitochondrially generated NO center dot also functions in extracellular hypoxic signaling pathways.
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