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胆汁盐输出泵(BSEP/ABCB11):转运和分拣障碍。

Bile salt export pump (BSEP/ABCB11): trafficking and sorting disturbances.

机构信息

Laboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan.

出版信息

Curr Mol Pharmacol. 2013 Jul;6(2):95-103. doi: 10.2174/18744672113069990036.

Abstract

Bile salt export pump (BSEP/ABCB11), a member of the family of ATP-binding cassette transporters, is localized on the canalicular membrane of hepatocytes and mediates the efficient biliary excretion of bile acid. The secretion of bile acid into bile by BSEP provides the primary osmotic driving force for bile flow generation. Intrahepatic cholestasis resulting from dysfunction of BSEP can be caused by a mutation in the gene encoding this protein or by acquired factors, such as the side effects of xenobiotics and drugs. In some pathophysiological states, inhibition of BSEP function is associated with its reduced expression on the canalicular membrane caused by impaired trafficking and sorting of BSEP. This fact has generated interest in better understanding the trafficking and sorting mechanism of BSEP. This review describes the molecular characteristics and physiological roles of BSEP, the trafficking and sorting machinery of BSEP, and the mechanisms responsible for disturbance of BSEP, which causes intrahepatic cholestasis.

摘要

胆盐输出泵(BSEP/ABCB11)是 ATP 结合盒转运蛋白家族的成员,位于肝细胞的胆小管膜上,介导胆汁酸的有效胆汁排泄。BSEP 将胆汁酸分泌到胆汁中,为胆汁流动的产生提供了主要的渗透驱动力。BSEP 编码基因的功能障碍或获得性因素(如外源性物质和药物的副作用)可导致 BSEP 引起的肝内胆汁淤积。在某些病理生理状态下,BSEP 功能的抑制与 BSEP 在胆小管膜上的表达减少有关,这是由于 BSEP 的运输和分拣受损所致。这一事实引起了人们对更好地理解 BSEP 的运输和分拣机制的兴趣。这篇综述描述了 BSEP 的分子特征和生理作用、BSEP 的运输和分拣机制,以及导致肝内胆汁淤积的 BSEP 紊乱的机制。

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