Electrolyte and Fluid Transport in Mesothelial Cells.

Hong-Long Ji, Hong-Guang Nie
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引用次数: 0

Abstract

Mesothelial cells are specialized epithelial cells, which line the pleural, pericardial, and peritoneal cavities. Accumulating evidence suggests that the monolayer of mesothelial cells is permeable to electrolyte and fluid, and thereby govern both fluid secretion and re-absorption in the serosal cavities. Disorders in these salt and fluid transport systems may be fundamental in the pathogenesis of pleural effusion, pericardial effusion, and ascites. In this review, we discuss the location, physiological function, and regulation of active transport (Na(+)-K(+)-ATPase) systems, cation and anion channels (Na(+), K(+), Cl(-), and Ca(2+) channels), antiport (exchangers) systems, and symport (co-transporters) systems, and water channels (aquaporins). These secretive and absorptive pathways across mesothelial monolayer cells for electrolytes and fluid may provide pivotal therapeutical targets for novel clinical intervention in edematous diseases of serous cavities.

间皮细胞中的电解质和液体运输。
间皮细胞是特化的上皮细胞,排列在胸膜腔、心包腔和腹膜腔内。越来越多的证据表明,单层间皮细胞可渗透电解质和液体,从而控制浆膜腔中的液体分泌和再吸收。这些盐和液体运输系统的紊乱可能是胸腔积液、心包积液和腹水发病的根本原因。在这篇综述中,我们讨论了主动运输(Na(+)-K(+)- atpase)系统,阳离子和阴离子通道(Na(+), K(+), Cl(-)和Ca(2+)通道),反端口(交换体)系统,同向(共转运体)系统和水通道(水通道蛋白)的位置,生理功能和调节。这些通过间皮单层细胞吸收电解质和液体的秘密途径可能为浆液腔水肿疾病的新型临床干预提供关键的治疗靶点。
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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