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多药耐药蛋白(MRP)介导的钙黄绿素ATP依赖性外排:细胞内谷胱甘肽耗竭无抑制作用。

ATP-dependent efflux of calcein by the multidrug resistance protein (MRP): no inhibition by intracellular glutathione depletion.

作者信息

Feller N, Broxterman H J, Währer D C, Pinedo H M

机构信息

Department of Medical Oncology, Free University Hospital, Amsterdam, The Netherlands.

出版信息

FEBS Lett. 1995 Jul 17;368(2):385-8. doi: 10.1016/0014-5793(95)00677-2.

Abstract

In this study we report that the multidrug resistance protein (MRP) transports calcein from the cytoplasmic compartment of tumor cells, in contrast to P-glycoprotein which transports calcein acetoxymethyl ester from the plasmamembrane. The transport of calcein by MRP is ATP-dependent and is inhibited by probenecid and vincristine. Intracellular glutathione (GSH) depletion which occurred when cells were exposed to buthionine sulfoximine had no effect on the efflux of calcein, whereas it reversed the daunorubicin accumulation deficit in MRP overexpressing tumor cells. In conclusion, ATP-dependent transport of calcein and possibly other organic anions by MRP is not inhibited by a large decrease of the intracellular GSH concentration, that inhibits daunorubicin efflux by MRP.

摘要

在本研究中,我们报告多药耐药蛋白(MRP)从肿瘤细胞的细胞质区室转运钙黄绿素,这与从质膜转运钙黄绿素乙酰氧甲酯的P-糖蛋白相反。MRP介导的钙黄绿素转运是ATP依赖性的,并受丙磺舒和长春新碱抑制。当细胞暴露于丁硫氨酸亚砜胺时发生的细胞内谷胱甘肽(GSH)耗竭对钙黄绿素外流没有影响,而它可逆转MRP过表达肿瘤细胞中柔红霉素蓄积不足的情况。总之,MRP介导的ATP依赖性钙黄绿素以及可能其他有机阴离子的转运不受细胞内GSH浓度大幅降低的抑制,而细胞内GSH浓度大幅降低会抑制MRP介导的柔红霉素外流。

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