TRPC channels and store-operated Ca2+ entry

被引:114
作者
Salido, Gines M. [1 ]
Sage, Stewart O. [2 ]
Rosado, Juan A. [1 ]
机构
[1] Univ Extremadura, Cell Physiol Res Grp, Dept Physiol, Caceres 10071, Spain
[2] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3EG, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2009年 / 1793卷 / 02期
关键词
TRPC; Store-operated Ca2+ entry; Type II IP3 receptor; STIM1; Orai1; CAPACITATIVE CALCIUM-ENTRY; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS; CA2+-PERMEABLE CATION CHANNEL; ENDOGENOUSLY EXPRESSED TRP1; SMOOTH-MUSCLE-CELLS; TRANSIENT-RECEPTOR; DROSOPHILA TRP; FUNCTIONAL EXPRESSION; CRAC CHANNELS; HUMAN HOMOLOG;
D O I
10.1016/j.bbamcr.2008.11.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Store-operated calcium entry (SOCE) is a major mechanism for Ca2+ influx. Since SOCE was first proposed two decades ago many techniques have been used in attempting to identify the nature of store-operated Ca2+ (SOC) channels. The first identified and best-characterised store-operated current is I-CRAC, but a number of other currents activated by Ca2+ store depletion have also been described. TRPC proteins have long been proposed as SOC channel candidates; however, whether any of the TRPCs function as SOC channels remains controversial. This review attempts to provide an overview of the arguments in favour and against the role of TRPC proteins in the store-operated mechanisms of agonist-activated Ca2+ entry. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:223 / 230
页数:8
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