Identification and Characterization of 3-Iodothyronamine Intracellular Transport

被引:28
作者
Ianculescu, Alexandra G. [2 ]
Giacomini, Kathleen M. [3 ]
Scanlan, Thomas S. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Portland, OR 97239 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
关键词
THYROID-HORMONE TRANSPORTERS; STEROID-HORMONES; HUMAN BRAIN; GENE; MUTATIONS; FAMILY;
D O I
10.1210/en.2008-1339
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
3-Iodothyronamine (T(1)AM) is a naturally occurring thyroid hormone metabolite with distinct biological effects that are opposite those of thyroid hormone. The known molecular targets of T(1)AM include both plasma membrane and intracellular proteins, suggesting that intracellular transport of T(1)AM may be an important component of its action, although no uptake mechanism has yet been described. Using various human cell lines, we show that, indeed, cellular uptake of T(1)AM occurs in multiple cell types and that this process involves specific, saturable, and inhibitable transport mechanisms. These mechanisms are sodium and chloride independent, pH dependent, thyronamine specific, and do not involve the likely candidate transporters of other monoamines, organic cations, or thyroid hormones. A large-scale RNA interference screen targeting the entire solute carrier superfamily of transporter genes reveals that the transport of T(1)AM into cells involves multiple transporters, and we identify eight transporters that may contribute to the uptake of T(1)AM in HeLa cells. This type of transporter small interfering RNA screening approach can be used in general to identify the constellation of transporters that participate in the intracellular disposition of compounds. (Endocrinology 150: 1991-1999, 2009)
引用
收藏
页码:1991 / 1999
页数:9
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