Chloride in Vesicular Trafficking and Function

被引:173
作者
Stauber, Tobias [1 ]
Jentsch, Thomas J.
机构
[1] Leibniz Inst Mol Pharmakol FMP, D-13125 Berlin, Germany
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 75 | 2013年 / 75卷
关键词
channelopathies; proximal tubular endocytosis; lysosome; neurotransmitter uptake; CLC transporter; CFTR; TRANSMEMBRANE CONDUCTANCE REGULATOR; RECEPTOR-MEDIATED ENDOCYTOSIS; LYSOSOMAL STORAGE DISEASE; CYSTIC-FIBROSIS; ENDOPLASMIC-RETICULUM; PLASMA-MEMBRANE; DENTS-DISEASE; ANION CHANNEL; MICE LACKING; ENDOSOMAL ACIDIFICATION;
D O I
10.1146/annurev-physiol-030212-183702
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Luminal acidification is of pivotal importance for the physiology of the secretory and endocytic pathways and its diverse trafficking events. Acidification by the proton-pumping V-ATPase requires charge compensation by counterion currents that are commonly attributed to chloride. The molecular identification of intracellular chloride transporters and the improvement of methodologies for measuring intraorganellar pH and chloride have facilitated the investigation of the physiology of vesicular chloride transport. New data question the requirement of chloride for pH regulation of various organelles and furthermore ascribe functions to chloride that are beyond merely electrically shunting the proton pump. This review surveys the currently established and proposed intracellular chloride transporters and gives an overview of membrane-trafficking steps that are affected by the perturbation of chloride transport. Finally, potential mechanisms of membrane-trafficking modulation by chloride are discussed and put into the context of organellar ion homeostasis in general.
引用
收藏
页码:453 / 477
页数:25
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