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使用TSPO配体靶向线粒体能量代谢。

Targeting mitochondrial energy metabolism with TSPO ligands.

作者信息

Gut Philipp

机构信息

Nestlé Institute of Health Sciences, EPFL Innovation Park, Bâtiment H, 1015 Lausanne, Switzerland

出版信息

Biochem Soc Trans. 2015 Aug;43(4):537-42. doi: 10.1042/BST20150019. Epub 2015 Aug 3.

Abstract

The translocator protein (18 kDa) (TSPO) resides on the outer mitochondrial membrane where it is believed to participate in cholesterol transport and steroid hormone synthesis. Although it is almost ubiquitously expressed, what TSPO does in non-steroidogenic tissues is largely unexplored. Recent studies report changes in glucose homoeostasis and cellular energy production when TSPO function is modulated by selective ligands or by genetic loss-of-function. This review summarizes findings that connect TSPO function with the regulation of mitochondrial energy metabolism. The juxtaposition of TSPO at the cytosolic/mitochondrial interface and the existence of endogenous ligands that are regulated by metabolism suggest that TSPO functions to adapt mitochondrial to cellular metabolism. From a pharmacological perspective the specific up-regulation of TSPO in neuro-inflammatory and injury-induced conditions make TSPO an interesting, druggable target of mitochondrial metabolism.

摘要

转位蛋白(18 kDa)(TSPO)位于线粒体外膜,据信它参与胆固醇转运和类固醇激素合成。尽管它几乎在所有组织中都有表达,但TSPO在非类固醇生成组织中的作用在很大程度上尚未得到探索。最近的研究报告称,当TSPO功能通过选择性配体或基因功能丧失进行调节时,葡萄糖稳态和细胞能量产生会发生变化。本综述总结了将TSPO功能与线粒体能量代谢调节联系起来的研究结果。TSPO在胞质/线粒体界面的并列以及受代谢调节的内源性配体的存在表明,TSPO的功能是使线粒体适应细胞代谢。从药理学角度来看,TSPO在神经炎症和损伤诱导条件下的特异性上调使其成为线粒体代谢中一个有趣的、可药物作用的靶点。

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