4.7 Review

Molecular Regulation of Canalicular ABC Transporters

期刊

出版社

MDPI
DOI: 10.3390/ijms22042113

关键词

bile secretion; ABCB1; ABCB4; ABCB11; ABCC2; ABCG5; G8; molecular partners

资金

  1. Ministere de l'Enseignement Superieur, de la Recherche et de l'Innovation
  2. German Research Foundation [403224013, SFB 1382, CRC296]
  3. Agence Nationale de la Recherche [ANR-15-CE14-0008-01]
  4. French Association for the Study of the Liver (AFEF)
  5. Fondation pour la Recherche Medicale [FRM-EQU-2020-03010517]
  6. Association Mucoviscidose-ABCF2
  7. Agence Nationale de la Recherche (ANR) [ANR-15-CE14-0008] Funding Source: Agence Nationale de la Recherche (ANR)

向作者/读者索取更多资源

ABC transporters expressed at the canalicular membrane of hepatocytes are crucial for bile secretion by secreting bile acids, phosphatidylcholine, cholesterol, drugs, and other compounds. Dysfunctions in these transporters lead to rare, severe biliary diseases, emphasizing the importance of studying their biology for developing new therapies.
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.

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