| Literature DB >> 14707014 |
Bernd Nilius1, Joris Vriens, Jean Prenen, Guy Droogmans, Thomas Voets.
Abstract
The vanilloid receptor-1 (VR1, now TRPV1) was the founding member of a subgroup of cation channels within the TRP family. The TRPV subgroup contains six mammalian members, which all function as Ca2+ entry channels gated by a variety of physical and chemical stimuli. TRPV4, which displays 45% sequence identity with TRPV1, is characterized by a surprising gating promiscuity: it is activated by hypotonic cell swelling, heat, synthetic 4alpha-phorbols, and several endogenous substances including arachidonic acid (AA), the endocannabinoids anandamide and 2-AG, and cytochrome P-450 metabolites of AA, such as epoxyeicosatrienoic acids. This review summarizes data on TRPV4 as a paradigm of gating diversity in this subfamily of Ca2+ entry channels.Entities:
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Year: 2004 PMID: 14707014 DOI: 10.1152/ajpcell.00365.2003
Source DB: PubMed Journal: Am J Physiol Cell Physiol ISSN: 0363-6143 Impact factor: 4.249