胆盐出口泵
胆汁淤积
胆汁酸
进行性家族性肝内胆汁淤积症
生物
ATP结合盒运输机
化学
运输机
生物化学
细胞生物学
内科学
内分泌学
医学
基因
肝移植
移植
作者
Hisamitsu Hayashi,Yuichi Sugiyama
标识
DOI:10.2174/18744672113069990036
摘要
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. Keywords: ATP-binding cassette (ABC) transporters, bile acid, bile formation, Bile Salt Export Pump (BSEP), cholestasis, protein trafficking, protein degradation.
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