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发育中小鼠心脏传导系统中的间隙连接连接蛋白

Gap junctional connexins in the developing mouse cardiac conduction system.

作者信息

Miquerol L, Dupays L, Théveniau-Ruissy M, Alcoléa S, Jarry-Guichard T, Abran P, Gros D

机构信息

Laboratoire de Génétique at Physiologie du Développement (CNRS UMR 6545), Institut de Biologie du Développement de Marseille, Université de la Méditerranée, Marseille, France.

出版信息

Novartis Found Symp. 2003;250:80-98; discussion 98-109, 276-9. doi: 10.1002/0470868066.ch6.

DOI:10.1002/0470868066.ch6
PMID:12956325
Abstract

Gap junctional channels which couple myocytes mediate conduction phenomena in the heart. These channels are dodecamers of transmembrane proteins belonging to the connexin family (Cx). Three Cxs, Cx43, -40 and -45, have been found to be expressed in cardiomyocytes. Each of them has a distinct spatiotemporal pattern of expression, which is regulated during development. In the adult mouse heart, Cx43 is expressed in all the working myocytes and most of the conductive myocytes; Cx45 is weakly expressed in all conductive myocytes, including those of the nodal tissues; Cx40 expression is restricted to the atria and ventricular conduction system. Analysis of mice with deletions of Cx genes has provided evidence that Cx43, -40 and -45, and consequently the gap junctional channels they form, are involved in both heart function and development. For example, Cx40 deficiency results in sinoatrial conduction impairments, a significant decrease of the conduction velocity in the atria, and a delay of the propagation of impulse in the His bundle. Transgenic mouse lines with modified Cx40 genes are now being used to draw up a detailed map of the conduction system in the adult and developing heart, and to identify the regulatory elements involved in the transcriptional regulation of the Cx40 gene. Some preliminary results of these studies are described.

摘要

连接心肌细胞的缝隙连接通道介导心脏中的传导现象。这些通道是属于连接蛋白家族(Cx)的跨膜蛋白的十二聚体。已发现三种连接蛋白,即Cx43、Cx40和Cx45,在心肌细胞中表达。它们各自具有独特的时空表达模式,在发育过程中受到调控。在成年小鼠心脏中,Cx43在所有工作心肌细胞和大多数传导心肌细胞中表达;Cx45在所有传导心肌细胞中表达较弱,包括节点组织的心肌细胞;Cx40的表达局限于心房和心室传导系统。对Cx基因缺失小鼠的分析提供了证据,表明Cx43、Cx40和Cx45,以及它们形成的缝隙连接通道,都参与心脏功能和发育。例如,Cx40缺乏会导致窦房传导障碍、心房传导速度显著降低以及希氏束中冲动传播延迟。现在正在使用具有修饰Cx40基因的转基因小鼠品系来绘制成年和发育中心脏传导系统的详细图谱,并确定参与Cx40基因转录调控的调控元件。本文描述了这些研究的一些初步结果。

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