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3-碘甲腺原氨酸胺细胞内转运的鉴定与特性分析

Identification and characterization of 3-iodothyronamine intracellular transport.

作者信息

Ianculescu Alexandra G, Giacomini Kathleen M, Scanlan Thomas S

机构信息

Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, California 94143, USA.

出版信息

Endocrinology. 2009 Apr;150(4):1991-9. doi: 10.1210/en.2008-1339. Epub 2008 Dec 12.

Abstract

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.

摘要

3-碘甲腺原氨酸(T(1)AM)是一种天然存在的甲状腺激素代谢产物,具有与甲状腺激素相反的独特生物学效应。T(1)AM已知的分子靶点包括质膜蛋白和细胞内蛋白,这表明T(1)AM的细胞内转运可能是其作用的重要组成部分,尽管尚未描述其摄取机制。使用多种人类细胞系,我们发现,实际上,T(1)AM在多种细胞类型中都存在细胞摄取,且该过程涉及特异性、可饱和且可抑制的转运机制。这些机制不依赖钠和氯,依赖pH,对甲腺原氨酸具有特异性,并且不涉及其他单胺、有机阳离子或甲状腺激素可能的候选转运体。针对整个溶质载体转运蛋白基因超家族进行的大规模RNA干扰筛选表明,T(1)AM进入细胞的转运涉及多种转运蛋白,并且我们鉴定出了八种可能有助于T(1)AM在HeLa细胞中摄取的转运蛋白。这种转运蛋白小干扰RNA筛选方法一般可用于鉴定参与化合物细胞内处置的转运蛋白组合。

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