| Literature DB >> 33672718 |
Amel Ben Saad1,2, Alix Bruneau2,3, Elodie Mareux1, Martine Lapalus1, Jean-Louis Delaunay2, Emmanuel Gonzales1,4, Emmanuel Jacquemin1,4, Tounsia Aït-Slimane2, Thomas Falguières1.
Abstract
The ATP-binding cassette (ABC) transporters expressed at the canalicular membrane of hepatocytes mediate the secretion of several compounds into the bile canaliculi and therefore play a key role in bile secretion. Among these transporters, ABCB11 secretes bile acids, ABCB4 translocates phosphatidylcholine and ABCG5/G8 is responsible for cholesterol secretion, while ABCB1 and ABCC2 transport a variety of drugs and other compounds. The dysfunction of these transporters leads to severe, rare, evolutionary biliary diseases. The development of new therapies for patients with these diseases requires a deep understanding of the biology of these transporters. In this review, we report the current knowledge regarding the regulation of canalicular ABC transporters' folding, trafficking, membrane stability and function, and we highlight the role of molecular partners in these regulating mechanisms.Entities:
Keywords: ABCB1; ABCB11; ABCB4; ABCC2; ABCG5/G8; bile secretion; molecular partners
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Year: 2021 PMID: 33672718 PMCID: PMC7924332 DOI: 10.3390/ijms22042113
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923