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理解物理屏障的概念障碍。

Conceptual barriers to understanding physical barriers.

作者信息

Lingaraju Amulya, Long Tiha M, Wang Yitang, Austin Jotham R, Turner Jerrold R

机构信息

Department of Pathology, The University of Chicago, United States.

Advanced Electron Microscopy Facility, Office of Shared Research Facilities, The University of Chicago, United States.

出版信息

Semin Cell Dev Biol. 2015 Jun;42:13-21. doi: 10.1016/j.semcdb.2015.04.008. Epub 2015 May 21.

Abstract

The members of the large family of claudin proteins regulate ion and water flux across the tight junction. Many claudins, e.g. claudins 2 and 15, accomplish this by forming size- and charge-selective paracellular channels. Claudins also appear to be essential for genesis of tight junction strands and recruitment of other proteins to these sites. What is less clear is whether claudins form the paracellular seal. While this seal is defective when claudins are disrupted, some results, including ultrastructural and biochemical data, suggest that lipid structures are an important component of tight junction strands and may be responsible for the paracellular seal. This review highlights current understanding of claudin contributions to barrier function and tight junction structure and suggests a model by which claudins and other tight junction proteins can drive assembly and stabilization of a lipid-based strand structure.

摘要

紧密连接蛋白大家族的成员调节离子和水通过紧密连接的通量。许多紧密连接蛋白,如紧密连接蛋白2和15,通过形成大小和电荷选择性的细胞旁通道来实现这一点。紧密连接蛋白对于紧密连接链的形成以及其他蛋白质募集到这些位点似乎也是必不可少的。尚不清楚的是紧密连接蛋白是否形成细胞旁密封。虽然当紧密连接蛋白被破坏时这种密封有缺陷,但一些结果,包括超微结构和生化数据,表明脂质结构是紧密连接链的重要组成部分,可能负责细胞旁密封。本综述强调了目前对紧密连接蛋白对屏障功能和紧密连接结构贡献的理解,并提出了一个模型,通过该模型紧密连接蛋白和其他紧密连接蛋白可以驱动基于脂质的链结构的组装和稳定。

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