多药耐药相关蛋白:谷胱甘肽、葡萄糖醛酸或硫酸盐结合物的外排泵。

Multidrug resistance-associated proteins: Export pumps for conjugates with glutathione, glucuronate or sulfate.

作者信息

Homolya László, Váradi András, Sarkadi Balázs

机构信息

Membrane Research Group, Hungarian Academy of Sciences, Budapest, Hungary.

出版信息

Biofactors. 2003;17(1-4):103-14. doi: 10.1002/biof.5520170111.

Abstract

Many endogenous or xenobiotic lipophilic substances are eliminated from the cells by the sequence of oxidation, conjugation to an anionic group (glutathione, glucuronate or sulfate) and transport across the plasma membrane into the extracellular space. The latter step is mediated by integral membrane glycoproteins belonging to the superfamily of ATP-Binding Cassette (ABC) transporters. A subfamily, referred as ABCC, includes the famous/infamous cystic fibrosis transmembrane regulator (CFTR), the sulfonylurea receptors (SUR 1 and 2), and the multidrug resistance-associated proteins (MRPs). The name of the MRPs refers to their potential role in clinical multidrug resistance, a phenomenon that hinders the effective chemotherapy of tumors. The MRPs that have been functionally characterized so far share the property of ATP-dependent export pumps for conjugates with glutathione (GSH), glucuronate or sulfate. MRP1 and MRP2 are also mediating the cotransport of unconjugated amphiphilic compounds together with free GSH. MRP3 preferentially transports glucuronides but not glutathione S-conjugates or free GSH. MRP1 and MRP2 also contribute to the control of the intracellular glutathione disulfide (GSSG) level. Although these proteins are low affinity GSSG transporters, they can play essential role in response to oxidative stress when the activity of GSSG reductase becomes rate limiting. The human MRP4, MRP5 and MRP6 have only partially been characterized. However, it has been revealed that MRP4 can function as an efflux pump for cyclic nucleotides and nucleoside analogues, used as anti-HIV drugs. MRP5 also transports GSH conjugates, nucleoside analogues, and possibly heavy metal complexes. Transport of glutathione S-conjugates mediated by MRP6, the mutation of which causes pseudoxantoma elasticum, has recently been shown. In summary, numerous members of the multidrug resistance-associated protein family serve as export pumps that prevent the accumulation of anionic conjugates and GSSG in the cytoplasm, and play, therefore, an essential role in detoxification and defense against oxidative stress.

摘要

许多内源性或外源性亲脂性物质通过氧化、与阴离子基团(谷胱甘肽、葡萄糖醛酸或硫酸盐)结合以及穿过质膜转运到细胞外空间的序列从细胞中清除。后一步由属于ATP结合盒(ABC)转运蛋白超家族的整合膜糖蛋白介导。一个亚家族,称为ABCC,包括著名的/声名狼藉的囊性纤维化跨膜调节因子(CFTR)、磺脲类受体(SUR 1和2)以及多药耐药相关蛋白(MRP)。MRP这个名称指的是它们在临床多药耐药中的潜在作用,这是一种阻碍肿瘤有效化疗的现象。迄今为止已在功能上得到表征的MRP具有作为与谷胱甘肽(GSH)、葡萄糖醛酸或硫酸盐结合物的ATP依赖性输出泵的特性。MRP1和MRP2还介导未结合的两亲性化合物与游离GSH的共转运。MRP3优先转运葡萄糖醛酸苷,但不转运谷胱甘肽S结合物或游离GSH。MRP1和MRP2也有助于控制细胞内谷胱甘肽二硫化物(GSSG)水平。尽管这些蛋白是低亲和力的GSSG转运蛋白,但当GSSG还原酶的活性成为限速因素时,它们在应对氧化应激中可发挥重要作用。人类MRP4、MRP5和MRP6仅得到部分表征。然而,已揭示MRP4可作为环核苷酸和核苷类似物(用作抗HIV药物)的外排泵发挥作用。MRP5也转运GSH结合物、核苷类似物以及可能的重金属复合物。最近已表明由MRP6介导的谷胱甘肽S结合物的转运,其突变会导致弹性假黄瘤。总之,多药耐药相关蛋白家族的众多成员作为输出泵,可防止阴离子结合物和GSSG在细胞质中积累,因此在解毒和抗氧化应激防御中发挥重要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索