In vivo role of CLC chloride channels in the kidney
- 1 November 2000
- journal article
- review article
- Published by American Physiological Society in American Journal of Physiology-Renal Physiology
- Vol. 279 (5), F802-F808
- https://doi.org/10.1152/ajprenal.2000.279.5.f802
Abstract
Chloride channels in the kidney are involved in important physiological functions such as cell volume regulation, acidification of intracellular vesicles, and transepithelial chloride transport. Among eight mammalian CLC chloride channels expressed in the kidney, three (CLC-K1, CLC-K2, and CLC-5) were identified to be related to kidney diseases in humans or mice. CLC-K1 mediates a transepithelial chloride transport in the thin ascending limb of Henle's loop and is essential for urinary concentrating mechanisms. CLC-K2 is a basolateral chloride channel in distal nephron segments and is necessary for chloride reabsorption. CLC-5 is a chloride channel in intracellular vesicles of proximal tubules and is involved in endocytosis. This review will cover the recent advances in research on the CLC chloride channels of the kidney with a special focus on the issues most necessary to understand their physiological roles in vivo, i.e., their intrarenal and cellular localization and their phenotypes of humans and mice that have their loss-of-function mutations.Keywords
This publication has 53 references indexed in Scilit:
- Disruption of clh-1, a chloride channel gene, results in a wider body of Caenorhabditis elegansJournal of Molecular Biology, 1999
- Molecular Cloning of CLC Chloride Channels inOreochromis Mossambicusand Their Functional Complementation of YeastCLCGene MutantBiochemical and Biophysical Research Communications, 1999
- Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent’sJapan diseaseKidney International, 1998
- Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disordersHuman Molecular Genetics, 1997
- Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).Journal of Clinical Investigation, 1997
- Identification of a New Outwardly Rectifying Cl− Channel That Belongs to a Subfamily of the ClC Cl− ChannelsPublished by Elsevier ,1996
- ClC‐6 and ClC‐7 are two novel broadly expressed members of the CLC chloride channel familyFEBS Letters, 1995
- Cloning and Functional Expression of Rat CLC-5, a Chloride Channel Related to Kidney DiseasePublished by Elsevier ,1995
- Cl- channels in basolateral renal medullary vesicles X. Cloning of a Cl- channel from rabbit outer medullaKidney International, 1995
- A chloride channel widely expressed in epithelial and non-epithelial cellsNature, 1992