| Literature DB >> 17217079 |
K Kiselyov1, D M Shin, J Y Kim, J P Yuan, S Muallem.
Abstract
TRP channels, in particular the TRPC and TRPV subfamilies, have emerged as important constituents of the receptor-activated Ca2+ influx mechanism triggered by hormones, growth factors, and neurotransmitters through activation ofphospholipase C (PLC). Several TRPC channels are also activated by passive depletion of endoplasmic reticulum (ER) Ca2+. Although in several studies the native TRP channels faithfully reproduce the respective recombinant channels, more often the properties of Ca2+ entry and/or the store-operated current are strikingly different from that of the TRP channels expressed in the same cells. The present review aims to discuss this disparity in the context of interaction of TRPC channels with auxiliary proteins that may alter the permeation and regulation of TRPC channels.Entities:
Mesh：
Substances：
Year: 2007 PMID： 17217079 DOI： 10.1007/978-3-540-34891-7_33
Source DB: PubMed Journal: Handb Exp Pharmacol ISSN： 0171-2004