Modulation of connexin 43 in viral infections

IF 4.7 Q1 VIROLOGY Tumour Virus Research Pub Date : 2024-11-08 DOI:10.1016/j.tvr.2024.200296
Harry Scott , Patricia E. Martin , Sheila V. Graham
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Abstract

Connexins are essential for intercellular communication through gap junctions and the maintenance of cellular and tissue homeostasis. Connexin 43 (Cx43) is the most ubiquitously expressed connexin. As well as regulating homeostasis, Cx43 hemichannels and gap junctions play important roles in inflammation and the immune response. This, coupled with a range of non-channel functions performed by Cx43 makes it an attractive target for viruses. Recently, several groups have begun to explore the relationship between Cx43 and viral infection, with a diverse array of viruses being found to alter Cx43 hemichannels/gap junctions. Importantly, this includes several small DNA tumour viruses, which may target Cx43 to promote tumorigenesis. This review focuses on the ability of selected RNA/DNA viruses and retroviruses to either positively or negatively regulate Cx43 hemichannels and gap junctions in order to carry out their lifecycles. The role of Cx43 regulation by tumour viruses is also discussed in relation to tumour progression.
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在病毒感染中调节连接蛋白 43
连接蛋白对于通过缝隙连接进行细胞间通信以及维持细胞和组织的平衡至关重要。连接蛋白 43(Cx43)是最普遍表达的连接蛋白。除了调节体内平衡外,Cx43 半通道和间隙连接还在炎症和免疫反应中发挥重要作用。这一点,再加上 Cx43 的一系列非通道功能,使其成为一个有吸引力的病毒靶标。最近,一些研究小组开始探索 Cx43 与病毒感染之间的关系,发现各种病毒都能改变 Cx43 半通道/间隙连接。重要的是,其中包括几种小型 DNA 肿瘤病毒,它们可能以 Cx43 为靶点促进肿瘤发生。本综述将重点讨论某些 RNA 和 DNA 病毒为完成其生命周期而对 Cx43 半通道和间隙连接进行正向或负向调节的能力。此外,还讨论了肿瘤病毒对 Cx43 调节的作用与肿瘤进展的关系。
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来源期刊
Tumour Virus Research
Tumour Virus Research Medicine-Infectious Diseases
CiteScore
6.50
自引率
2.30%
发文量
16
审稿时长
56 days
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