The 190-kDa multidrug resistance protein (MRP) has recently been associated with the transport of cysteinyl leukotrienes and several glutathione (GSH) S-conjugates. In the present study, we have examined the transport of leukotriene C-4 (LTC(4)) in membrane vesicles from MRP-transfected HeLa cells (T14), as well as drug-selected H69AR lung cancer cells which express high levels of MRP. V-max and K-m values for LTC(4) transport by membrane vesicles from T14 cells were 529 +/- 176 pmol mg(-1) min(-1) and 105 +/- 31 nM, respectively, At 50 nM LTC(4), the K-m (ATP) was 70 mu M. Transport in T14 vesicles was osmotically-sensitive and was supported by various nucleoside triphosphates but not by non- or slowly-hydrolyzable ATP analogs, LTC, transport rates in membrane vesicles derived from H69AR cells and their parental and revertant variants were consistent with their relative levels of MRP expression. A 190-kDa protein in T14 membrane vesicles was photolabeled by [H-3]LTC(4) and immunoprecipitation with MRP-specific monoclonal antibodies (mAbs) confirmed that this protein was MRP, LTC, transport was inhibited by an MRP-specific mAb (QCRL-3) directed against an intracellular conformational epitope of MRP, but not by a mAb (QCRL-1) which recognizes a linear epitope, Photolabeling with [H-3]LTC(4) was also inhibitable by mAb QCRL-3 but not mAb &CRL-I, GSH did not inhibit LTC, transport, However, the ability of alkylated GSH derivatives to inhibit transport increased markedly with the length of the alkyl group, S-Decylglutathione was a potent competitive inhibitor of [H-3]LTC(4) transport (K-i(app) 116 nM), suggesting that the two compounds bind to the same, or closely related, site(s) on MRP. Chemotherapeutic agents including colchicine, doxorubicin, and daunoru bicin were poor inhibitors of [H-3]LTC, transport, Taxol, VP-16, vincristine, and vinblastine were also poor inhibitors of LTC, transport but inhibition by these compounds was enhanced by GSH. Uptake of[H-3]vincristine into T14 membrane vesicles in the absence of GSB was low and not dependent on ATP, However, in the presence of GSH, ATP-dependent vincristine transport was observed, Levels of transport increased with concentrations of GSH up to 5 mM. The identification of an MRP-specific mAb that inhibits LTC, transport and prevents photolabeling of MRP by LTC(4), provides conclusive evidence of the ability of MRP to transport cysteinyl leukotrienes, Our studies also demonstrate that MRP is capable of mediating ATP-dependent transport of vincristine and that transport is GSH-dependent.
