Biosynthesis and trafficking of the bile salt export pump, BSEP: therapeutic implications of BSEP mutations.

Carol J Soroka, James L Boyer

Journal: Molecular aspects of medicine 2014;37():3-14

PMID: 23685087

Abstract

The bile salt export pump (BSEP, ABCB11) is the primary transporter of bile acids from the hepatocyte to the biliary system. This rate-limiting step in bile formation is essential to the formation of bile salt dependent bile flow, the enterohepatic circulation of bile acids, and the digestion of dietary fats. Mutations in BSEP are associated with cholestatic diseases such as progressive familial intrahepatic cholestasis type 2 (PFIC2), benign recurrent intrahepatic cholestasis type 2 (BRIC2), drug-induced cholestasis, and intrahepatic cholestasis of pregnancy. Development of clinical therapies for these conditions necessitates a clear understanding of the cell biology of biosynthesis, trafficking, and transcriptional and translational regulation of BSEP. This chapter will focus on the molecular and cell biological aspects of this critical hepatic membrane transporter.

Copyright © 2013 Elsevier Ltd. All rights reserved.

Address: Yale University School of Medicine, Department of Internal Medicine, New Haven, CT 06520, United States. Electronic address: [email protected].; Yale University School of Medicine, Department of Internal Medicine, New Haven, CT 06520, United States. Electronic address: [email protected].
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