The solute carrier family SLC10: more than a family of bile acid transporters regarding function and phylogenetic relationships

被引:181
作者
Geyer, J
Wilke, T
Petzinger, E
机构
[1] Univ Giessen, Inst Pharmakol & Toxikol, D-35392 Giessen, Germany
[2] Univ Giessen, Inst Allgemeine & Spezielle Zool, D-35392 Giessen, Germany
关键词
solute carrier family 10; Na+/taurocholate cotransporting polypeptide; apical sodium-dependent bile acid transporter; sodium-dependent organic anion transporter; taurocholate; oestrone-3-sulfate; dehydroepiandrosterone sulfate; phylogeny;
D O I
10.1007/s00210-006-0043-8
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The solute carrier family 10 (SLC10) comprises two sodium-dependent bile acid transporters, i.e. the Na+/ taurocholate cotransporting polypeptide (NTCP ; SLC10A1) and the apical sodium-dependent bile acid transporter ( ASBT; SLC10A2). These carriers are essentially involved in the maintenance of the enterohepatic circulation of bile acids mediating the first step of active bile acid transport through the membrane barriers in the liver ( NTCP) and intestine ( ASBT). Recently, four new members of the SLC10 family were described and referred to as P3 (SLC10A3), P4 (SLC10A4), P5 (SLC10A5) and sodium-dependent organic anion transporter ( SOAT; SLC10A6). Experimental data supporting carrier function of P3, P4, and P5 is currently not available. However, as demonstrated for SOAT, not all members of the SLC10 family are bile acid transporters. SOAT specifically transports steroid sulfates such as oestrone-3-sulfate and dehydroepiandrosterone sulfate in a sodium-dependent manner, and is considered to play an important role for the cellular delivery of these prohormones in testes, placenta, adrenal gland and probably other peripheral tissues. ASBT and SOAT are the most homologous members of the SLC10 family, with high sequence similarity (similar to 70%) and almost identical gene structures. Phylogenetic analyses of the SLC10 family revealed that ASBT and SOAT genes emerged from a common ancestor gene. Structure - activity relationships of NTCP, ASBT and SOAT are discussed at the amino acid sequence level. Based on the high structural homology between ASBT and SOAT, pharmacological inhibitors of the ASBT, which are currently being tested in clinical trials for cholesterol-lowering therapy, should be evaluated for their cross-reactivity with SOAT.
引用
收藏
页码:413 / 431
页数:19
相关论文
共 113 条
[1]
Plastid genome phylogeny and a model of amino acid substitution for proteins encoded by chloroplast DNA [J].
Adachi, J ;
Waddell, PJ ;
Martin, W ;
Hasegawa, M .
JOURNAL OF MOLECULAR EVOLUTION, 2000, 50 (04) :348-358
[2]
CPG ISLANDS OF THE X-CHROMOSOME ARE GENE ASSOCIATED [J].
ALCALAY, M ;
TONIOLO, D .
NUCLEIC ACIDS RESEARCH, 1988, 16 (20) :9527-9543
[3]
Functional expression of the apical Na+-dependent bile acid transporter in large but not small rat cholangiocytes [J].
Alpini, G ;
Glaser, SS ;
Rodgers, R ;
Phinizy, JL ;
Robertson, WE ;
Lasater, J ;
Caligiuri, A ;
Tretjak, Z ;
LeSage, GD .
GASTROENTEROLOGY, 1997, 113 (05) :1734-1740
[4]
CHARACTERIZATION OF CLONED RAT-LIVER NA+-BILE ACID COTRANSPORTER USING PEPTIDE AND FUSION PROTEIN ANTIBODIES [J].
ANANTHANARAYANAN, M ;
NG, OC ;
BOYER, JL ;
SUCHY, FJ .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1994, 267 (04) :G637-G643
[5]
Dephosphorylation of Ser-226 facilitates plasma membrane retention of Ntcp [J].
Anwer, MS ;
Gillin, H ;
Mukhopadhyay, S ;
Balasubramaniyam, N ;
Suchy, FJ ;
Ananthanarayanan, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (39) :33687-33692
[7]
Neither intestinal sequestration of bile acids nor common bile duct ligation modulate the expression and function of the rat ileal bile acid transporter [J].
Arrese, M ;
Trauner, M ;
Sacchiero, RJ ;
Crossman, MW ;
Shneider, BL .
HEPATOLOGY, 1998, 28 (04) :1081-1087
[8]
Site-directed mutagenesis and use of bile acid-MTS conjugates to probe the role of cysteines in the human apical sodium-dependent bile acid transporter (SLC10A2) [J].
Banerjee, A ;
Ray, A ;
Chang, C ;
Swaan, PW .
BIOCHEMISTRY, 2005, 44 (24) :8908-8917
[9]
Baringhaus KH, 1999, J LIPID RES, V40, P2158
[10]
Dehydroepiandrosterone (DHEA): A fountain of youth? [J].
Baulieu, EE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (09) :3147-3151