Identification of thyroid hormone transporters

被引:128
作者
Friesema, ECH
Docter, R
Moerings, EPCM
Stieger, B
Hagenbuch, B
Meier, PJ
Krenning, EP
Hennemann, G
Visser, TJ [1 ]
机构
[1] Erasmus Univ, Sch Med, Dept Internal Med 3, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus Univ, Sch Med, Dept Nucl Med, NL-3000 DR Rotterdam, Netherlands
[3] Univ Zurich Hosp, Dept Med, Div Clin Pharmacol & Toxicol, CH-8091 Zurich, Switzerland
关键词
D O I
10.1006/bbrc.1998.9974
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
Thyroid hormone action and metabolism are intracellular events that require transport of the hormone across the plasma membrane. We tested the possible involvement of the Na+/taurocholate cotransporting polypeptide (Ntcp) and organic anion transporting polypeptide (oatp1) in the hepatic uptake of the prohormone T4, the active hormone T3, and the metabolites rT3 and 3,3'-T2. Xenopus laevis oocytes were injected with 2.3 ng Ntcp or oatp1 cRNA and, after 2-3 days, incubated for 1 h at 25 degrees C with usually 0.1 mu M I-125-labeled ligand. Uninjected oocytes showed marked uptake of iodothyronines and this was further increased by Ntcp and oatp1 cRNA, i.e., 1.9- and 2.8-fold for T4, 1.7- and 1.7-fold for T3, 1.8- and 6.0-fold for rT3, and 1.3- and 1.4-fold for 3,3'-T2, respectively. Mostly due to much lower uptake by uninjected oocytes, Ntcp and oatp1 cRNA induced larger, 12- to 76-fold increases in uptake of iodothyronine sulfates. The Ntcp cRNA-induced iodothyronine uptake was completely inhibited in Na+-deplete medium, whereas the oatp1 cRNA-induced uptake was not affected. These results suggest that hepatic uptake of thyroid hormones and their metabolites is mediated at least in part by Ntcp and oatp1. (C) 1999 Academic Press.
引用
收藏
页码:497 / 501
页数:5
相关论文
共 36 条
[1]   Molecular characterization and tissue distribution of a new organic anion transporter subtype (oatp3) that transports thyroid hormones and taurocholate and comparison with oatp2 [J].
Abe, T ;
Kakyo, M ;
Sakagami, H ;
Tokui, T ;
Nishio, T ;
Tanemoto, M ;
Nomura, H ;
Hebert, SC ;
Matsuno, S ;
Kondo, H ;
Yawo, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (35) :22395-22401
[2]  
[Anonymous], [No title captured]
[3]  
Bossuyt X, 1996, J PHARMACOL EXP THER, V276, P891
[4]   Multispecific amphipathic substrate transport by an organic anion transporter of human liver [J].
Bossuyt, X ;
Muller, M ;
Meier, PJ .
JOURNAL OF HEPATOLOGY, 1996, 25 (05) :733-738
[5]   Expression and transport properties of the human ileal and renal sodium-dependent bile acid transporter [J].
Craddock, AL ;
Love, MW ;
Daniel, RW ;
Kirby, LC ;
Walters, HC ;
Wong, MH ;
Dawson, PA .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 274 (01) :G157-G169
[6]   Expression of rat liver cell membrane transporters for thyroid hormone in Xenopus laevis oocytes [J].
Docter, R ;
Friesema, ECH ;
VanStralen, PGJ ;
Krenning, EP ;
Everts, ME ;
Visser, TJ ;
Hennemann, G .
ENDOCRINOLOGY, 1997, 138 (05) :1841-1846
[8]   Rapid sulfation of 3,3′,5′-triiodothyronine in native Xenopus laevis oocytes [J].
Friesema, ECH ;
Docter, R ;
Krenning, EP ;
Everts, ME ;
Hennemann, G ;
Visser, TJ .
ENDOCRINOLOGY, 1998, 139 (02) :596-600
[9]  
FRIESEMA ECH, 1998, J ENDOCRINOL INVES S, V21, P77
[10]  
FRIESEMA ECH, 1997, J ENDOCRINOL INVES S, V20, P34