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CLC氯离子通道家族。

The CLC chloride channel family.

作者信息

Jentsch T J, Friedrich T, Schriever A, Yamada H

机构信息

Zentrum für Molekulare Neurobiologie, (ZMNH) Universität Hamburg, Martinistrasse 85, D-20246 Hamburg, Germany.

出版信息

Pflugers Arch. 1999 May;437(6):783-95. doi: 10.1007/s004240050847.

Abstract

Chloride channels perform important roles in the regulation of cellular excitability, in transepithelial transport, cell volume regulation, and acidification of intracellular organelles. This variety of functions requires a large number of different chloride channels that are encoded by genes belonging to several unrelated gene families. The CLC family of chloride channels has nine known members in mammals that show a differential tissue distribution and function both in plasma membranes and in intracellular organelles. CLC proteins have about 10-12 transmembrane domains. They probably function as dimers and may have two pores. The functional expression of channels altered by site-directed mutagenesis has led to important insights into their structure-function relationship. Their physiological relevance is obvious from three human inherited diseases (myotonia congenita, Dent's disease and Bartter's syndrome) that result from mutations in some of their members and from a knock-out mouse model.

摘要

氯离子通道在调节细胞兴奋性、跨上皮运输、细胞容积调节以及细胞内细胞器酸化过程中发挥着重要作用。这些多样的功能需要大量不同的氯离子通道,它们由属于几个不相关基因家族的基因编码。哺乳动物中已知的氯离子通道CLC家族有九个成员,它们在质膜和细胞内细胞器中表现出不同的组织分布和功能。CLC蛋白有大约10 - 12个跨膜结构域。它们可能以二聚体形式发挥作用,并且可能有两个孔道。通过定点诱变改变通道的功能表达,有助于深入了解其结构与功能的关系。从三种人类遗传性疾病(先天性肌强直、丹特病和巴特综合征)以及一种基因敲除小鼠模型可以明显看出它们的生理相关性,这些疾病是由该家族某些成员的突变引起的。

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