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瞬时受体电位阳离子通道亚家族C成员3(TRPC3):一种多功能转导分子,参与细胞信号的整合与多样化。

TRPC3: a versatile transducer molecule that serves integration and diversification of cellular signals.

作者信息

Groschner Klaus, Rosker Christian

机构信息

Institute of Pharmaceutical Sciences, Pharmacology and Toxicology, Karl-Franzens-University of Graz, Universitätsplatz 2, 8010, Graz, Austria.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2005 Apr;371(4):251-6. doi: 10.1007/s00210-005-1054-6.

DOI:10.1007/s00210-005-1054-6
PMID:15889239
Abstract

Transient receptor potential (TRP) proteins have been recognized as sensors for a wide variety of external and internal signals involved in maintenance of cellular homeostasis and control of physiological functions. Evidence of a striking versatility in terms of signal integration and transduction has been reported for members of the canonical (or classical) TRP subfamily (TRPCs). TRPC species are cation channel subunits and emerge as multifunctional signal transduction molecules that are able to function as components of divergent signalplexes. Results obtained in heterologous expression systems suggest TRPC3 as a paradigm of multifunctional signal transduction by a cation channel protein. TRPC3 serves cellular Ca(2+) signaling by multiple mechanisms and may control a variety of distinct physiological functions. In this review, we summarize current knowledge on the properties and possible signaling partners of TRPC3, and discuss the role of TRPC3 channel proteins in cellular signaling networks.

摘要

瞬时受体电位(TRP)蛋白已被公认为是多种外部和内部信号的传感器,这些信号参与细胞稳态的维持和生理功能的调控。关于典型(或经典)TRP亚家族(TRPCs)成员在信号整合和转导方面具有显著多功能性的证据已有报道。TRPC种类是阳离子通道亚基,作为多功能信号转导分子出现,能够作为不同信号复合体的组成部分发挥作用。在异源表达系统中获得的结果表明,TRPC3是阳离子通道蛋白进行多功能信号转导的一个范例。TRPC3通过多种机制参与细胞钙(Ca2+)信号传导,并可能控制多种不同的生理功能。在本综述中,我们总结了关于TRPC3的特性和可能的信号传导伙伴的当前知识,并讨论了TRPC3通道蛋白在细胞信号网络中的作用。

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Polymodal TRPC signaling: Emerging role in phenotype switching and tissue remodeling.多模式瞬时受体电位通道C(TRPC)信号传导:在表型转换和组织重塑中的新作用
Commun Integr Biol. 2010 Sep;3(5):393-5. doi: 10.4161/cib.3.5.12131.
2
TRPC3 regulates agonist-stimulated Ca2+ mobilization by mediating the interaction between type I inositol 1,4,5-trisphosphate receptor, RACK1, and Orai1.TRPC3 通过介导 I 型肌醇 1,4,5-三磷酸受体、RACK1 和 Orai1 之间的相互作用调节激动剂刺激的 Ca2+ 动员。
J Biol Chem. 2010 Mar 12;285(11):8045-53. doi: 10.1074/jbc.M109.033605. Epub 2009 Dec 18.
3
Complex regulation of the TRPC3, 6 and 7 channel subfamily by diacylglycerol and phosphatidylinositol-4,5-bisphosphate.

本文引用的文献

1
Functional characterization and physiological relevance of the TRPC3/6/7 subfamily of cation channels.阳离子通道TRPC3/6/7亚家族的功能特性及生理相关性
Naunyn Schmiedebergs Arch Pharmacol. 2005 Apr;371(4):257-65. doi: 10.1007/s00210-005-1052-8.
2
Enhanced expression of transient receptor potential channels in idiopathic pulmonary arterial hypertension.瞬时受体电位通道在特发性肺动脉高压中的表达增强
Proc Natl Acad Sci U S A. 2004 Sep 21;101(38):13861-6. doi: 10.1073/pnas.0405908101. Epub 2004 Sep 9.
3
VAMP2-dependent exocytosis regulates plasma membrane insertion of TRPC3 channels and contributes to agonist-stimulated Ca2+ influx.
二酰基甘油和磷脂酰肌醇-4,5-二磷酸对瞬时受体电位通道3、6和7亚家族的复杂调控
Cell Calcium. 2008 May;43(5):506-14. doi: 10.1016/j.ceca.2007.09.001. Epub 2007 Oct 17.
4
Transient receptor potential (TRP) channels as drug targets.
Naunyn Schmiedebergs Arch Pharmacol. 2006 Jul;373(4):271-2. doi: 10.1007/s00210-006-0071-4.
5
Functional characterization and physiological relevance of the TRPC3/6/7 subfamily of cation channels.阳离子通道TRPC3/6/7亚家族的功能特性及生理相关性
Naunyn Schmiedebergs Arch Pharmacol. 2005 Apr;371(4):257-65. doi: 10.1007/s00210-005-1052-8.
6
Structure-function analysis of TRPV channels.瞬时受体电位香草酸亚型(TRPV)通道的结构-功能分析
Naunyn Schmiedebergs Arch Pharmacol. 2005 Apr;371(4):285-94. doi: 10.1007/s00210-005-1053-7.
7
The TRPC2 ion channel and pheromone sensing in the accessory olfactory system.瞬时受体电位通道2(TRPC2)离子通道与副嗅觉系统中的信息素感知
Naunyn Schmiedebergs Arch Pharmacol. 2005 Apr;371(4):245-50. doi: 10.1007/s00210-005-1028-8.
8
Regulation of TRPM2 channels in neutrophil granulocytes by ADP-ribose: a promising pharmacological target.ADP-核糖对中性粒细胞中TRPM2通道的调节:一个有前景的药理学靶点。
Naunyn Schmiedebergs Arch Pharmacol. 2005 Apr;371(4):325-33. doi: 10.1007/s00210-005-1033-y.
9
TRP channels as new pharmacological targets.
Naunyn Schmiedebergs Arch Pharmacol. 2005 Apr;371(4):241-4. doi: 10.1007/s00210-005-1029-7.
VAMP2 依赖性胞吐作用调节 TRPC3 通道的质膜插入,并促进激动剂刺激的 Ca2+ 内流。
Mol Cell. 2004 Aug 27;15(4):635-46. doi: 10.1016/j.molcel.2004.07.010.
4
Junctate is a key element in calcium entry induced by activation of InsP3 receptors and/or calcium store depletion.连接蛋白是由肌醇三磷酸受体激活和/或钙库耗竭诱导的钙内流的关键元件。
J Cell Biol. 2004 Aug 16;166(4):537-48. doi: 10.1083/jcb.200404079. Epub 2004 Aug 9.
5
A TRPC1/TRPC3-mediated increase in store-operated calcium entry is required for differentiation of H19-7 hippocampal neuronal cells.H19-7海马神经元细胞分化需要TRPC1/TRPC3介导的储存式钙内流增加。
J Biol Chem. 2004 Oct 15;279(42):43392-402. doi: 10.1074/jbc.M408959200. Epub 2004 Aug 5.
6
Obligatory role of Src kinase in the signaling mechanism for TRPC3 cation channels.Src激酶在TRPC3阳离子通道信号传导机制中的必要作用。
J Biol Chem. 2004 Sep 24;279(39):40521-8. doi: 10.1074/jbc.M405280200. Epub 2004 Jul 22.
7
Role of TRP channels in oxidative stress.瞬时受体电位通道在氧化应激中的作用。
Novartis Found Symp. 2004;258:222-30; discussion 231-5, 263-6.
8
Ca(2+) signaling by TRPC3 involves Na(+) entry and local coupling to the Na(+)/Ca(2+) exchanger.TRPC3介导的钙离子信号传导涉及钠离子内流以及与钠钙交换体的局部偶联。
J Biol Chem. 2004 Apr 2;279(14):13696-704. doi: 10.1074/jbc.M308108200. Epub 2004 Jan 21.
9
N-linked protein glycosylation is a major determinant for basal TRPC3 and TRPC6 channel activity.N-连接蛋白糖基化是基础TRPC3和TRPC6通道活性的主要决定因素。
J Biol Chem. 2003 Nov 28;278(48):47842-52. doi: 10.1074/jbc.M302983200. Epub 2003 Sep 11.
10
TRPC3-like protein is involved in the capacitative cation entry induced by 1alpha,25-dihydroxy-vitamin D3 in ROS 17/2.8 osteoblastic cells.TRPC3样蛋白参与1α,25-二羟基维生素D3诱导的ROS 17/2.8成骨细胞中的容量性阳离子内流。
J Cell Biochem. 2003 Sep 1;90(1):197-205. doi: 10.1002/jcb.10612.