The SLC10 Carrier Family: Transport Functions and Molecular Structure

被引:101
作者
Doering, Barbara [1 ]
Luetteke, Thomas [2 ]
Geyer, Joachim [1 ]
Petzinger, Ernst [1 ]
机构
[1] Univ Giessen, Biomed Res Ctr BFS, Inst Pharmacol & Toxicol, Family Res Grp SLC10, D-35390 Giessen, Germany
[2] Univ Giessen, Inst Vet Physiol & Biochem, D-35390 Giessen, Germany
来源
CO-TRANSPORT SYSTEMS | 2012年 / 70卷
关键词
BILE-ACID TRANSPORTER; TAUROCHOLATE COTRANSPORTING POLYPEPTIDE; ORGANIC ANION TRANSPORTER; SALT EXPORT PUMP; FARNESOID-X-RECEPTOR; LOWERS PLASMA-CHOLESTEROL; REDUCES SERUM-CHOLESTEROL; HIGH-AFFINITY TRANSPORTER; BORDER MEMBRANE-VESICLES; ISOLATED RAT HEPATOCYTES;
D O I
10.1016/B978-0-12-394316-3.00004-1
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 SLC10 family represents seven genes containing 1-12 exons that encode proteins in humans with sequence lengths of 348-477 amino acids. Although termed solute carriers (SLCs), only three out of seven (i.e. SLC10A1, SLC10A2, and SLC10A6) show sodium-dependent uptake of organic substrates across the cell membrane. These include the uptake of bile salts, sulfated steroids, sulfated thyroidal hormones, and certain statin drugs by SLC10A1 (Na+-taurocholate cotransporting polypeptide (NTCP)), the uptake of bile salts by SLC10A2 (apical sodium-dependent bile acid transporter (ASBT)), and uptake of sulfated steroids and sulfated taurolithocholate by SLC10A6 (sodium-dependent organic anion transporter (SOAT)). The other members of the family are orphan carriers not all localized in the cell membrane. The name "bile acid transporter family" arose because the first two SLC10 members (NTCP and ASBT) are carriers for bile salts that establish their enterohepatic circulation. In recent years, information has been obtained on their 2D and 3D membrane topology, structure transport relationships, and on the ligand and sodium-binding sites. For SLC10A2, the putative 3D morphology was deduced from the crystal structure of a bacterial SLC10A2 analog, ASBT(NM). This information was used in this chapter to calculate the putative 3D structure of NTCP. This review provides first an introduction to recent knowledge about bile acid synthesis and newly found bile acid hormonal functions, and then describes step-by-step each individual member of the family in terms of expression, localization, substrate pattern, as well as protein topology with emphasis on the three functional SLC10 carrier members.
引用
收藏
页码:105 / 168
页数:64
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