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平滑肌细胞中储存操纵性TRPC通道的多种激活机制。

Multiple activation mechanisms of store-operated TRPC channels in smooth muscle cells.

作者信息

Albert A P, Saleh S N, Peppiatt-Wildman C M, Large W A

机构信息

Ion Channel and Cell Signalling, Division of Basic Medical Sciences, St George's, University of London, Cranmer Terrace, London SW17 ORE, UK.

出版信息

J Physiol. 2007 Aug 15;583(Pt 1):25-36. doi: 10.1113/jphysiol.2007.137802. Epub 2007 Jul 5.

Abstract

Store-operated channels (SOCs) are plasma membrane Ca2+-permeable cation channels which are activated by agents that deplete intracellular Ca2+ stores. In smooth muscle SOCs are involved in contraction, gene expression, cell growth and proliferation. Single channel recording has demonstrated that SOCs with different biophysical properties are expressed in smooth muscle indicating diverse molecular identities. Moreover it is apparent that several gating mechanisms including calmodulin, protein kinase C and lysophospholipids are involved in SOC activation. Evidence is accumulating that TRPC proteins are important components of SOCs in smooth muscle. More recently Orai and STIM proteins have been proposed to underlie the well-described calcium-release-activated current (ICRAC) in non-excitable cells but at present there is little information on the role of Orai and STIM proteins in smooth muscle. In addition it is likely that different TRPC subunits coassemble as heterotetrameric structures to form smooth muscle SOCs. In this brief review we summarize the diverse properties and gating mechanisms of SOCs in smooth muscle. We propose that the heterogeneity of the properties of these conductances in smooth muscle results from the formation of heterotetrameric TRPC structures in different smooth muscle preparations.

摘要

储存操纵性通道(SOCs)是质膜上的钙离子通透阳离子通道,可被耗尽细胞内钙离子储存的因子激活。在平滑肌中,SOCs参与收缩、基因表达、细胞生长和增殖。单通道记录表明,具有不同生物物理特性的SOCs在平滑肌中表达,这表明其分子身份多样。此外,很明显,包括钙调蛋白、蛋白激酶C和溶血磷脂在内的几种门控机制参与了SOCs的激活。越来越多的证据表明,瞬时受体电位通道蛋白(TRPC)是平滑肌中SOCs的重要组成部分。最近,有人提出Orai蛋白和基质相互作用分子(STIM)蛋白是不可兴奋细胞中描述详尽的钙释放激活电流(ICRAC)的基础,但目前关于Orai蛋白和STIM蛋白在平滑肌中的作用的信息很少。此外,不同的TRPC亚基可能共同组装成异源四聚体结构,形成平滑肌SOCs。在这篇简短的综述中,我们总结了平滑肌中SOCs的多种特性和门控机制。我们认为,平滑肌中这些电导特性的异质性是由不同平滑肌制剂中异源四聚体TRPC结构的形成导致的。

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