SLC13 family of Na+-coupled di- and tri-carboxylate/sulfate transporters

被引:97
作者
Bergeron, M. J. [1 ]
Clemencon, B. [2 ]
Hediger, M. A. [2 ]
Markovich, D. [3 ]
机构
[1] Univ Laval, CRIUSMQ, Axe Neurosci Cellulaires & Mol, Quebec City, PQ G1J 2G3, Canada
[2] Univ Bern, Natl Ctr Competence Res NCCR TransCure, Inst Biochem & Mol Med, CH-3012 Bern, Switzerland
[3] Univ Queensland, Sch Biomed Sci, Mol Physiol Grp, St Lucia, Qld 4072, Australia
基金
瑞士国家科学基金会;
关键词
DEPENDENT DICARBOXYLATE TRANSPORTER; COTRANSPORTER GENE NAS1; ACETYL-L-ASPARTATE; CITRATE TRANSPORTER; HIGH-AFFINITY; GENOMIC ORGANIZATION; SULFATE TRANSPORTER; EXPRESSION CLONING; FUNCTIONAL-CHARACTERIZATION; NA+/DICARBOXYLATE COTRANSPORTER;
D O I
10.1016/j.mam.2012.12.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The SLC13 family comprises five genes (SLC13A1, SLC13A2, SLC13A3, SLC13A4, and SLC13A5) encoding structurally related multi-spanning transporters (8-13 transmembrane domains) with orthologues found in prokaryotes and eukaryotes. Mammalian SLC13 members mediate the electrogenic Na+-coupled anion cotransport at the plasma membrane of epithelial cells (mainly kidney, small intestine, placenta and liver) or cells of the central nervous system. While the two SLC13 cotransporters NaS1 (SLC13A1) and NaS2 (SLC13A4) transport anions such sulfate, selenate and thiosulfate, the three other SLC13 members, NaDC1 (SLC13A2), NaCT (SLC13A5) and NaDC3 (SLC13A3), transport di- and tri-carboxylate Krebs cycle intermediates such as succinate, citrate and alpha-ketoglutarate. All these transporters play a variety of physiological and pathophysiological roles in the different organs. Thus, the purpose of this review is to summarize the roles of SLC13 members in human physiology and pathophysiology and what the therapeutic perspectives are. We have also described the most recent advances on the structure, expression, function and regulation of SLC13 transporters. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:299 / 312
页数:14
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