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连接蛋白的异源混合:伙伴兼容性及功能后果

Heteromeric mixing of connexins: compatibility of partners and functional consequences.

作者信息

Beyer E C, Gemel J, Martínez A, Berthoud V M, Valiunas V, Moreno A P, Brink P R

机构信息

Department of Pediatrics, University of Chicago, IL 60637-1470, USA.

出版信息

Cell Commun Adhes. 2001;8(4-6):199-204. doi: 10.3109/15419060109080723.

Abstract

Cx43 is widely expressed in many different cell types, and many of these cells also express other connexins. If these connexins are capable of mixing, the functional properties of channels containing heteromeric connexons may substantially influence intercellular communication between such cells. We used biochemical strategies (sedimentation through sucrose gradients, co-immunoprecipitation, or co-purification by Ni-NTA chromatography) to examine heteromeric mixing of Cx43 with other connexins (including Cx26, Cx37, Cx40, Cx45, and Cx56) in transfected cells. These analyses showed that all of the tested connexins except Cx26 formed heteromeric connexons with Cx43. We used the double whole-cell patch-camp technique to analyze the electrophysiological properties of gap junction channels in pairs of co-expressing cells. Cx37 and Cx45 made a large variety of functional heteromeric combinations with Cx43 based on detection of many different single channel conductances. Most of the channel event sizes observed in cells co-expressing Cx40 and Cx43 were similar to those of homomeric Cx43 or Cx40 hemichannels in homo- or hetero-typic configurations. Our data suggest several different possible consequences of connexin co-expression: (1) some combinations of connexins may form heteromeric connexons with novel proeprties; (2) some connexins may form heteromeric channels that do not have unique properties, and (3) some connexins may be incompatible for heteromeric mixing.

摘要

Cx43在许多不同细胞类型中广泛表达,并且这些细胞中的许多也表达其他连接蛋白。如果这些连接蛋白能够混合,那么包含异源连接子的通道的功能特性可能会显著影响此类细胞之间的细胞间通讯。我们使用生化策略(通过蔗糖梯度沉降、免疫共沉淀或镍-次氮基三乙酸层析共纯化)来检测转染细胞中Cx43与其他连接蛋白(包括Cx26、Cx37、Cx40、Cx45和Cx56)的异源混合情况。这些分析表明,除Cx26外,所有测试的连接蛋白都与Cx43形成了异源连接子。我们使用双全细胞膜片钳技术来分析共表达细胞对中缝隙连接通道的电生理特性。基于对许多不同单通道电导的检测,Cx37和Cx45与Cx43形成了多种功能性异源组合。在共表达Cx40和Cx43的细胞中观察到的大多数通道事件大小与同型或异型配置中的同源Cx43或Cx40半通道相似。我们的数据表明连接蛋白共表达可能有几种不同的后果:(1)某些连接蛋白组合可能形成具有新特性的异源连接子;(2)某些连接蛋白可能形成没有独特特性的异源通道,以及(3)某些连接蛋白可能不适合异源混合。

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