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荷电选择性紧密连接通道

Charge-selective claudin channels.

机构信息

Institute of Clinical Physiology, Charité- Universitätsmedizin Berlin, Freie Universität and Humboldt Universität, Berlin, Germany.

出版信息

Ann N Y Acad Sci. 2012 Jun;1257:20-8. doi: 10.1111/j.1749-6632.2012.06555.x.

Abstract

Claudins are the main determinants of barrier properties of the tight junction. Many claudins have been shown to act by tightening the paracellular pathway, but several function as paracellular channels. While some depend on the endogenous claudin background of the analyzed cell line, for other claudins, a distinct charge-selectivity has been shown. This paper portrays cation-selective (claudin-2, claudin-10b, claudin-15) and anion-selective (claudin-10a, claudin-17) claudins and claudins with debatable channel properties (claudin-4, claudin-7, claudin-16). It also describes molecular properties determining the observed charge-selectivity and pore properties in general. In leaky tissues, they widely determine overall transport characteristics by providing paracellular ion-selective pathways. In small intestine, claudin-2 and claudin-15 replace each other in the developing gut. In kidney proximal tubules, claudin-2, claudin-10, and claudin-17 allow for paracellular reabsorption of sodium, chloride, and water.

摘要

紧密连接的紧密连接是屏障特性的主要决定因素。许多紧密连接蛋白被证明可以通过收紧细胞旁途径来发挥作用,但也有一些作为细胞旁通道发挥作用。虽然一些紧密连接蛋白依赖于分析细胞系中内源性紧密连接蛋白的背景,但对于其他紧密连接蛋白,已经显示出明显的电荷选择性。本文描述了阳离子选择性(claudin-2、claudin-10b、claudin-15)和阴离子选择性(claudin-10a、claudin-17)紧密连接蛋白以及具有争议性通道特性的紧密连接蛋白(claudin-4、claudin-7、claudin-16)。它还描述了决定观察到的电荷选择性和一般孔隙特性的分子特性。在渗漏组织中,它们通过提供细胞旁离子选择性途径广泛决定整体转运特性。在小肠中,claudin-2 和 claudin-15 在发育中的肠道中相互替代。在肾脏近端小管中,claudin-2、claudin-10 和 claudin-17 允许钠、氯和水通过细胞旁重吸收。

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