TRPA1 underlies a sensing mechanism for O2

Nat Chem Biol. 2011 Aug 28;7(10):701-11. doi: 10.1038/nchembio.640.

Abstract

Oxygen (O(2)) is a prerequisite for cellular respiration in aerobic organisms but also elicits toxicity. To understand how animals cope with the ambivalent physiological nature of O(2), it is critical to elucidate the molecular mechanisms responsible for O(2) sensing. Here our systematic evaluation of transient receptor potential (TRP) cation channels using reactive disulfides with different redox potentials reveals the capability of TRPA1 to sense O(2). O(2) sensing is based upon disparate processes: whereas prolyl hydroxylases (PHDs) exert O(2)-dependent inhibition on TRPA1 activity in normoxia, direct O(2) action overrides the inhibition via the prominent sensitivity of TRPA1 to cysteine-mediated oxidation in hyperoxia. Unexpectedly, TRPA1 is activated through relief from the same PHD-mediated inhibition in hypoxia. In mice, disruption of the Trpa1 gene abolishes hyperoxia- and hypoxia-induced cationic currents in vagal and sensory neurons and thereby impedes enhancement of in vivo vagal discharges induced by hyperoxia and hypoxia. The results suggest a new O(2)-sensing mechanism mediated by TRPA1.

MeSH terms

  • Animals
  • Cells, Cultured
  • Humans
  • Hypoxia
  • Mice
  • Mice, Knockout
  • Molecular Structure
  • Oxygen / chemistry
  • Oxygen / metabolism*
  • Procollagen-Proline Dioxygenase / chemistry
  • Procollagen-Proline Dioxygenase / metabolism
  • Stereoisomerism
  • TRPA1 Cation Channel
  • Transient Receptor Potential Channels / chemistry
  • Transient Receptor Potential Channels / deficiency
  • Transient Receptor Potential Channels / metabolism*

Substances

  • TRPA1 Cation Channel
  • Transient Receptor Potential Channels
  • Trpa1 protein, mouse
  • Procollagen-Proline Dioxygenase
  • Oxygen