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作为感染因子靶点的紧密连接

Tight junctions as targets of infectious agents.

作者信息

Guttman Julian A, Finlay B Brett

机构信息

Simon Fraser University, Department of Biological Sciences, Shrum Science Centre, Burnaby, BC, Canada V5A 1S6.

出版信息

Biochim Biophys Acta. 2009 Apr;1788(4):832-41. doi: 10.1016/j.bbamem.2008.10.028. Epub 2008 Nov 14.

Abstract

The epithelial barrier is a critical border that segregates luminal material from entering tissues. Essential components of this epithelial fence are physical intercellular structures termed tight junctions. These junctions use a variety of transmembrane proteins coupled with cytoplasmic adaptors, and the actin cytoskeleton, to attach adjacent cells together thereby forming intercellular seals. Breaching of this barrier has profound effects on human health and disease, as barrier deficiencies have been linked with the onset of inflammation, diarrhea generation and pathogenic effects. Although tight junctions efficiently restrict most microbes from penetrating into deeper tissues and contain the microbiota, some pathogens have developed specific strategies to alter or disrupt these structures as part of their pathogenesis, resulting in either pathogen penetration, or other consequences such as diarrhea. Understanding the strategies that microorganisms use to commandeer the functions of tight junctions is an active area of research in microbial pathogenesis. In this review we highlight and overview the tactics bacteria and viruses use to alter tight junctions during disease. Additionally, these studies have identified novel tight junction protein functions by using pathogens and their virulence factors as tools to study the cell biology of junctional structures.

摘要

上皮屏障是一个关键边界,可将管腔物质与进入组织隔离开来。这个上皮屏障的重要组成部分是称为紧密连接的物理细胞间结构。这些连接使用多种跨膜蛋白,结合细胞质衔接子和肌动蛋白细胞骨架,将相邻细胞连接在一起,从而形成细胞间密封。破坏这个屏障会对人类健康和疾病产生深远影响,因为屏障缺陷与炎症发作、腹泻产生和致病作用有关。虽然紧密连接有效地限制了大多数微生物渗透到更深的组织中并容纳微生物群,但一些病原体已经制定了特定策略来改变或破坏这些结构,作为其发病机制的一部分,导致病原体渗透或其他后果,如腹泻。了解微生物用于操纵紧密连接功能的策略是微生物发病机制研究的一个活跃领域。在这篇综述中,我们重点介绍并概述了细菌和病毒在疾病过程中改变紧密连接的策略。此外,这些研究通过使用病原体及其毒力因子作为研究连接结构细胞生物学的工具,确定了紧密连接蛋白的新功能。

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