Zaman G J, Lankelma J, van Tellingen O, Beijnen J, Dekker H, Paulusma C, Oude Elferink R P, Baas F, Borst P
Division of Molecular Biology, Netherlands Cancer Institute, Amsterdam.
Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7690-4. doi: 10.1073/pnas.92.17.7690.
Multidrug-resistance-associated protein (MRP) is a plasma membrane glycoprotein that can confer multidrug resistance (MDR) by lowering intracellular drug concentration. Here we demonstrate that depletion of intracellular glutathione by DL-buthionine (S,R)-sulfoximine results in a complete reversal of resistance to doxorubicin, daunorubicin, vincristine, and VP-16 in lung carcinoma cells transfected with a MRP cDNA expression vector. Glutathione depletion had less effect on MDR in cells transfected with MDR1 cDNA encoding P-glycoprotein and did not increase the passive uptake of daunorubicin by cells, indicating that the decrease of MRP-mediated MDR was not due to nonspecific membrane damage. Glutathione depletion resulted in a decreased efflux of daunorubicin from MRP-transfected cells, but not from MDR1-transfected cells, suggesting that glutathione is specifically required for the export of drugs from cells by MRP. We also show that MRP increases the export of glutathione from the cell and this increased export is further elevated in the presence of arsenite. Our results support the hypothesis that MRP functions as a glutathione S-conjugate carrier.
多药耐药相关蛋白(MRP)是一种质膜糖蛋白,可通过降低细胞内药物浓度赋予多药耐药性(MDR)。在此我们证明,用DL-丁硫氨酸(S,R)-亚砜亚胺消耗细胞内谷胱甘肽会导致转染了MRP cDNA表达载体的肺癌细胞对阿霉素、柔红霉素、长春新碱和依托泊苷的耐药性完全逆转。谷胱甘肽消耗对转染了编码P-糖蛋白的MDR1 cDNA的细胞中的MDR影响较小,且不会增加细胞对柔红霉素的被动摄取,这表明MRP介导的MDR降低并非由于非特异性膜损伤。谷胱甘肽消耗导致柔红霉素从转染了MRP的细胞中的外排减少,但从转染了MDR1的细胞中未减少,这表明谷胱甘肽是MRP将药物从细胞中输出所特需的。我们还表明,MRP增加了谷胱甘肽从细胞中的输出,并且在亚砷酸盐存在下这种增加的输出会进一步升高。我们的结果支持MRP作为谷胱甘肽S-共轭载体发挥作用的假说。