Castillo G, Vera J C, Yang C P, Horwitz S B, Rosen O M
Program in Molecular Biology, Memorial Sloan-Kettering Cancer Research Center, New York, NY 10021.
Proc Natl Acad Sci U S A. 1990 Jun;87(12):4737-41. doi: 10.1073/pnas.87.12.4737.
The development of multidrug resistance (MDR) is associated with the overproduction of a plasma membrane glycoprotein, P glycoprotein. Here we report the functional expression of a member of the murine mdr family of proteins and show that Xenopus oocytes injected with RNA encoding the mouse mdr1b P glycoprotein develop a MDR-like phenotype. Immunological analysis indicated that oocytes injected with the mdr1b RNA synthesized a protein with the size and immunological characteristics of the mouse mdr1b P glycoprotein. These oocytes exhibited a decreased accumulation of [3H]vinblastine and showed an increased capacity to extrude the drug compared to control oocytes not expressing the P glycoprotein. In addition, competition experiments indicated that verapamil, vincristine, daunomycin, and quinidine, but not colchicine, can overcome the rapid drug efflux conferred by the expression of the mouse P glycoprotein.
多药耐药性(MDR)的产生与一种质膜糖蛋白P糖蛋白的过量表达有关。在此,我们报道了鼠源mdr蛋白家族中一个成员的功能性表达,并表明注射编码小鼠mdr1b P糖蛋白RNA的非洲爪蟾卵母细胞呈现出类似MDR的表型。免疫分析表明,注射mdr1b RNA的卵母细胞合成了一种具有小鼠mdr1b P糖蛋白大小和免疫特性的蛋白质。与未表达P糖蛋白的对照卵母细胞相比,这些卵母细胞中[3H]长春碱的积累减少,且药物外排能力增强。此外,竞争实验表明,维拉帕米、长春新碱、柔红霉素和奎尼丁(但秋水仙碱不能)能够克服小鼠P糖蛋白表达所赋予的快速药物外排。