Multidrug resistance protein 4 (MRP4/ABCC4) mediates efflux of bimane-glutathione.

Article Details

Citation

Bai J, Lai L, Yeo HC, Goh BC, Tan TM

Multidrug resistance protein 4 (MRP4/ABCC4) mediates efflux of bimane-glutathione.

Int J Biochem Cell Biol. 2004 Feb;36(2):247-57.

PubMed ID
14643890 [ View in PubMed
]
Abstract

Multidrug resistance proteins (MRPs) are ATP-dependent export pumps that mediate the export of organic anions. ABCC1 (MRP1), ABCC2 (MRP2) and ABCC3 (MRP3) are all able to facilitate the efflux of anionic conjugates including glutathione (GSH), glucuronide and sulfate conjugates of xenobiotics and endogenous molecules. Earlier studies showed that ABCC4 functions as an ATP-driven export pump for cyclic AMP and cyclic GMP, as well as estradiol-17-beta-D-glucuronide. However, it was unclear if other conjugated metabolites can be transported by ABCC4. Hence in this study, a fluorescent substrate, bimane-glutathione (bimane-GS) was used to further examine the transport activity of ABCC4. Using cells stably overexpressing ABCC4, this study shows that ABCC4 can facilitate the efflux of the glutathione conjugate, bimane-glutathione. Bimane-glutathione efflux increased with time and >85% of the conjugate was exported after 15min. This transport was abolished in the presence of 2.5microM carbonylcyanide m-chlorophenylhydrasone (CCCP), an uncoupler of oxidative phosphorylation. Inhibition was also observed with known inhibitors of MRP transporters including benzbromarone, verapamil and indomethacin. In addition, 100microM methotrexate, an ABCC4 substrate or 100microM 6-thioguanine (6-TG), a compound whose monophosphate metabolite is an ABCC4 substrate, reduced efflux by >40%. A concentration-dependent inhibition of bimane-glutathione efflux was observed with 1-chloro-2,4-dinitrobenzene (CDNB) which is metabolized intracellularly to the glutathione conjugate, 2,4-dinitrophenyl-glutathione (DNP-GS). The determination that ABCC4 can mediate the transport of glucuronide and glutathione conjugates indicates that ABCC4 may play a role in the cellular extrusion of Phase II detoxification metabolites.

DrugBank Data that Cites this Article

Drug Transporters
DrugTransporterKindOrganismPharmacological ActionActions
Cholic AcidMultidrug resistance-associated protein 4ProteinHumans
Unknown
Inhibitor
Details
IndomethacinMultidrug resistance-associated protein 4ProteinHumans
Unknown
Inhibitor
Details
MethotrexateMultidrug resistance-associated protein 4ProteinHumans
Unknown
Substrate
Inhibitor
Details
TioguanineMultidrug resistance-associated protein 4ProteinHumans
Unknown
Inhibitor
Details
VerapamilMultidrug resistance-associated protein 4ProteinHumans
Unknown
Inhibitor
Details