The SLC3 and SLC7 families of amino acid transporters

被引:526
作者
Fotiadis, Dimitrios [1 ,2 ]
Kanai, Yoshikatsu [3 ]
Palacin, Manuel [4 ,5 ]
机构
[1] Univ Bern, Inst Biochem & Mol Med, CH-3012 Bern, Switzerland
[2] Univ Bern, Swiss Natl Ctr Competence Res NCCR TransCure, CH-3012 Bern, Switzerland
[3] Osaka Univ, Dept Pharmacol, Grad Sch Med, Div Biosyst Pharmacol, Osaka, Japan
[4] Univ Barcelona, Fac Biol, Dept Biochem & Mol Biol, Inst Res Biomed IRB Barcelona, E-08028 Barcelona, Spain
[5] Ctr Invest Biomed Red Enfermedades Raras, E-08028 Barcelona, Spain
基金
瑞士国家科学基金会; 日本学术振兴会;
关键词
Aminoacidurias; Cancer; Cationic amino acid transporter; Heteromeric amino acid transporter; L-Type amino acid transporter; SLC3; SLC7; LYSINURIC PROTEIN INTOLERANCE; CYSTINE/GLUTAMATE EXCHANGE TRANSPORTER; 4F2; HEAVY-CHAIN; GENOTYPE-PHENOTYPE CORRELATION; SYSTEM X(C)(-); OXIDATIVE STRESS; EXTRACELLULAR GLUTAMATE; FUNCTIONAL-ANALYSIS; MEMBRANE-PROTEIN; CD98; EXPRESSION;
D O I
10.1016/j.mam.2012.10.007
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
Amino acids are necessary for all living cells and organisms. Specialized transporters mediate the transfer of amino acids across plasma membranes. Malfunction of these proteins can affect whole-body homoeostasis giving raise to diverse human diseases. Here, we review the main features of the SLC3 and SLC7 families of amino acid transporters. The SLC7 family is divided into two subfamilies, the cationic amino acid transporters (CATs), and the L-type amino acid transporters (LATs). The latter are the light or catalytic subunits of the heteromeric amino acid transporters (HATs), which are associated by a disulfide bridge with the heavy subunits 4F2hc or rBAT. These two subunits are glycoproteins and form the SLC3 family. Most CAT subfamily members were functionally characterized and shown to function as facilitated diffusers mediating the entry and efflux of cationic amino acids. In certain cells, CATs play an important role in the delivery of L-arginine for the synthesis of nitric oxide. HATs are mostly exchangers with a broad spectrum of substrates and are crucial in renal and intestinal re-absorption and cell redox balance. Furthermore, the role of the HAT 4F2hc/LAT1 in tumor growth and the application of LAT1 inhibitors and PET tracers for reduction of tumor progression and imaging of tumors are discussed. Finally, we describe the link between specific mutations in HATs and the primary inherited aminoacidurias, cystinuria and lysinuric protein intolerance. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:139 / 158
页数:20
相关论文
共 189 条
[1]  
[Anonymous], 2001, METABOLIC MOL BASES
[2]   Neuroadaptations in cystine-glutamate exchange underlie cocaine relapse [J].
Baker, DA ;
McFarland, K ;
Lake, RW ;
Shen, H ;
Tang, XC ;
Toda, S ;
Kalivas, PW .
NATURE NEUROSCIENCE, 2003, 6 (07) :743-749
[3]   In Lysinuric Protein Intolerance system y+L activity is defective in monocytes and in GM-CSF-differentiated macrophages [J].
Barilli, Amelia ;
Rotoli, Bianca Maria ;
Visigalli, Rossana ;
Bussolati, Ovidio ;
Gazzola, Gian C. ;
Kadija, Zamir ;
Rodi, Giuseppe ;
Mariani, Francesca ;
Ruzza, Maria Lorena ;
Luisetti, Maurizio ;
Dall'Asta, Valeria .
ORPHANET JOURNAL OF RARE DISEASES, 2010, 5
[4]   Distinct classes of trafficking rBAT mutants cause the type I cystinuria phenotype [J].
Bartoccioni, Paola ;
Rius, Monica ;
Zorzano, Antonio ;
Palacin, Manuel ;
Chillaron, Josep .
HUMAN MOLECULAR GENETICS, 2008, 17 (12) :1845-1854
[5]   Role of Transmembrane Domain 8 in Substrate Selectivity and Translocation of SteT, a Member of the L-Amino Acid Transporter (LAT) Family [J].
Bartoccioni, Paola ;
del Rio, Cesar ;
Ratera, Merce ;
Kowalczyk, Lukasz ;
Baldwin, Jocelyn M. ;
Zorzano, Antonio ;
Quick, Matthias ;
Baldwin, Stephen A. ;
Luis Vazquez-Ibar, Jose ;
Palacin, Manuel .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (37) :28764-28776
[6]   Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system xc- [J].
Bassi, MT ;
Gasol, E ;
Manzoni, M ;
Pineda, M ;
Riboni, M ;
Martín, R ;
Zorzano, A ;
Borsani, G ;
Palacín, M .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2001, 442 (02) :286-296
[7]   Functional cooperation of epithelial heteromeric amino acid transporters expressed in madin-darby canine kidney cells [J].
Bauch, C ;
Forster, N ;
Loffing-Cueni, D ;
Summa, V ;
Verrey, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (02) :1316-1322
[8]   Apical heterodimeric cystine and cationic amino acid transporter expressed in MDCK cells [J].
Bauch, C ;
Verrey, F .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2002, 283 (01) :F181-F189
[9]   TEXtopo:: shaded membrane protein topology plots in LATEX2ε [J].
Beitz, E .
BIOINFORMATICS, 2000, 16 (11) :1050-1051
[10]   EXPRESSION CLONING OF A CDNA FROM RABBIT KIDNEY CORTEX THAT INDUCES A SINGLE TRANSPORT-SYSTEM FOR CYSTINE AND DIBASIC AND NEUTRAL AMINO-ACIDS [J].
BERTRAN, J ;
WERNER, A ;
MOORE, ML ;
STANGE, G ;
MARKOVICH, D ;
BIBER, J ;
TESTAR, X ;
ZORZANO, A ;
PALACIN, M ;
MURER, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) :5601-5605