到插入椎间盘的贩运高速公路:解锁连接蛋白43定位特异性的新见解。

Q2 Biochemistry, Genetics and Molecular Biology Cell Communication and Adhesion Pub Date : 2014-02-01 DOI:10.3109/15419061.2013.876014
Shan-Shan Zhang, Robin M Shaw
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引用次数: 20

摘要

每次心跳时,数十亿个心肌细胞协同工作,传播有效循环血液所需的电兴奋。连接蛋白的调控表达和及时传递,在特殊的细胞-细胞接触区形成间隙连接,被称为嵌入盘,对心室心肌细胞偶联至关重要。我们将重点回顾最近发现的连接蛋白43 (Cx43)生命周期的几种调控机制,Cx43是心肌中寿命短且表达最丰富的连接蛋白。Cx43的生命周期始于基因表达,随后寡聚化成六聚体通道,然后以细胞骨架为基础向椎间盘区域运输。一旦传递,半通道与驻留的盘蛋白相互作用,并被组织以影响细胞间偶联。我们重点介绍了最近探索Cx43定位到嵌入椎间盘的调控的研究,重点是Cx43异构体的交替翻译和细胞骨架运输机制,它们共同调节心肌细胞之间的Cx43间隙连接偶联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Trafficking highways to the intercalated disc: new insights unlocking the specificity of connexin 43 localization.

With each heartbeat, billions of cardiomyocytes work in concert to propagate the electrical excitation needed to effectively circulate blood. Regulated expression and timely delivery of connexin proteins to form gap junctions at the specialized cell-cell contact region, known as the intercalated disc, is essential to ventricular cardiomyocyte coupling. We focus this review on several regulatory mechanisms that have been recently found to govern the lifecycle of connexin 43 (Cx43), the short-lived and most abundantly expressed connexin in cardiac ventricular muscle. The Cx43 lifecycle begins with gene expression, followed by oligomerization into hexameric channels, and then cytoskeletal-based transport toward the disc region. Once delivered, hemichannels interact with resident disc proteins and are organized to effect intercellular coupling. We highlight recent studies exploring regulation of Cx43 localization to the intercalated disc, with emphasis on alternatively translated Cx43 isoforms and cytoskeletal transport machinery that together regulate Cx43 gap junction coupling between cardiomyocytes.

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来源期刊
Cell Communication and Adhesion
Cell Communication and Adhesion 生物-生化与分子生物学
CiteScore
2.50
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation Cell Communication and Adhesion is an international Open Access journal which provides a central forum for research on mechanisms underlying cellular signalling and adhesion. The journal provides a single source of information concerning all forms of cellular communication, cell junctions, adhesion molecules and families of receptors from diverse biological systems. The journal welcomes submission of original research articles, reviews, short communications and conference reports.
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