The canalicular multidrug resistance protein, cMRP/MRP2, a novel conjugate export pump expressed in the apical membrane of hepatocytes
- PMID: 9381978
- DOI: 10.1016/s0065-2571(96)00013-1
The canalicular multidrug resistance protein, cMRP/MRP2, a novel conjugate export pump expressed in the apical membrane of hepatocytes
Abstract
The conjugate export pump in the hepatocyte canalicular membrane is, together with the ATP-dependent bile salt export pump, one of the two major pumps determining canalicular anion secretion and bile flow. The so-called bile salt-independent bile flow is largely driven by the cmrp/cmoat gene-encoded conjugate export pump, as indicated by the markedly reduced bile flow in the GY/TR- (11, 13-16) and the EHBR mutant rats (18-20). The importance of conjugation with glutathione (52, 53), glucuronate (11, 21), and sulfate (11, 16) for transfer of endogenous and xenobiotic substances from blood into bile has long been known. The molecular identification (7, 26, 54) and cloning (9, 10, 30) of the ATP-dependent export pump for these conjugates in the canalicular membrane was, at least in part, a consequence of the elucidation of the substrate specificity of the multidrug resistance protein (MRP) which is very similar to that of its canalicular isoform (3-6, 49). The broad substrate specificity of the conjugate export pump enables the terminal excretion of a multitude of conjugates and amphiphilic anions which are formed by a large number of relatively specific monooxygenases and transferases in phase I and phase II metabolism of endogenous and xenobiotic substances in the hepatocyte. The predominant expression of the conjugate export pump encoded by the cmrp/cmoat gene in the canalicular membrane does not exclude overexpression of this transporter in other cells and tissues when exposed to drugs and toxins that can be excreted by this pump. The apical conjugate export pump (8-10) may thus confer multidrug resistance to tumor cells in a similar manner as MRP1 (55). The observation that mRNA encoding rat cMrp/cMoat (10, 12) and its rabbit homolog (35) is not only detected in hepatocytes but also in small intestine and the kidneys suggests that the cmrp/cmoat gene-encoded conjugate export pump may function in the apical membrane domain of various epithelial cells.
Similar articles
-
The function of the multidrug resistance proteins (MRP and cMRP) in drug conjugate transport and hepatobiliary excretion.Adv Enzyme Regul. 1996;36:17-29. doi: 10.1016/0065-2571(95)00011-9. Adv Enzyme Regul. 1996. PMID: 8869738
-
Hepatic canalicular membrane 5: Expression and localization of the conjugate export pump encoded by the MRP2 (cMRP/cMOAT) gene in liver.FASEB J. 1997 Jun;11(7):509-16. doi: 10.1096/fasebj.11.7.9212074. FASEB J. 1997. PMID: 9212074 Review.
-
cDNA cloning of the hepatocyte canalicular isoform of the multidrug resistance protein, cMrp, reveals a novel conjugate export pump deficient in hyperbilirubinemic mutant rats.J Biol Chem. 1996 Jun 21;271(25):15091-8. doi: 10.1074/jbc.271.25.15091. J Biol Chem. 1996. PMID: 8662992
-
Expression of the MRP gene-encoded conjugate export pump in liver and its selective absence from the canalicular membrane in transport-deficient mutant hepatocytes.J Cell Biol. 1995 Oct;131(1):137-50. doi: 10.1083/jcb.131.1.137. J Cell Biol. 1995. PMID: 7559771 Free PMC article.
-
ATP-dependent transport of glutathione S-conjugates by the multidrug resistance protein MRP1 and its apical isoform MRP2.Chem Biol Interact. 1998 Apr 24;111-112:153-61. doi: 10.1016/s0009-2797(97)00158-0. Chem Biol Interact. 1998. PMID: 9679551 Review.
Cited by
-
In Vitro Stimulation of Multidrug Resistance-Associated Protein 2 Function Is Not Reproduced In Vivo in Rats.Pharmaceutics. 2018 Aug 8;10(3):125. doi: 10.3390/pharmaceutics10030125. Pharmaceutics. 2018. PMID: 30096834 Free PMC article.
-
Role of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia.Toxicol Appl Pharmacol. 2015 Nov 15;289(1):124-32. doi: 10.1016/j.taap.2015.08.018. Epub 2015 Sep 2. Toxicol Appl Pharmacol. 2015. PMID: 26342858 Free PMC article. Review.
-
Effect of adenovirus-mediated RNA interference on endogenous microRNAs in a mouse model of multidrug resistance protein 2 gene silencing.J Virol. 2006 Dec;80(24):12236-47. doi: 10.1128/JVI.01205-06. Epub 2006 Oct 4. J Virol. 2006. PMID: 17020948 Free PMC article.
-
Vinblastine pharmacokinetics in mouse, dog, and human in the context of a physiologically based model incorporating tissue-specific drug binding, transport, and metabolism.Pharmacol Res Perspect. 2023 Feb;11(1):e01052. doi: 10.1002/prp2.1052. Pharmacol Res Perspect. 2023. PMID: 36631976 Free PMC article.
-
Bile Acid-Drug Interaction via Organic Anion-Transporting Polypeptide 4C1 Is a Potential Mechanism of Altered Pharmacokinetics of Renally Excreted Drugs.Int J Mol Sci. 2022 Jul 31;23(15):8508. doi: 10.3390/ijms23158508. Int J Mol Sci. 2022. PMID: 35955643 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources