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pH敏感探针5-(及-6)-羧基萘并罗丹明荧光染料是多药耐药相关蛋白MRP1的一种底物。

The pH sensitive probe 5-(and-6)-carboxyl seminaphthorhodafluor is a substrate for the multidrug resistance-related protein MRP1.

作者信息

Jin Jing, Jones Arwyn T

机构信息

Welsh School of Pharmacy, Cardiff University, Cardiff, Wales, United Kingdom.

出版信息

Int J Cancer. 2009 Jan 1;124(1):233-8. doi: 10.1002/ijc.23892.

DOI:10.1002/ijc.23892
PMID:18924151
Abstract

Cellular function is dependent on tight regulation of intracellular pH and numerous reports show cancer cells have abnormal pH values in the cytosol and organelles, such as lysosomes. 5-(and-6)-carboxyl seminaphthorhodafluor (SNARF-1) is a commonly used pH sensitive probe and was used here to determine cytosolic pH of HL-60 leukemia cells and a drug-resistant variant overexpressing multidrug-resistance related protein 1 (MRP1). Resistant cells accumulated significantly less SNARF-1 compared to parental cells but near control levels of probe accumulation were observed by preincubating cells with the specific MRP1 inhibitor MK571. Two new drug-resistant cell lines were generated following exposure to doxorubicin or daunorubicin and these upregulated MRP1 or P-glycoprotein expression, respectively. Experiments in these cells showed that reduced SNARF-1 accumulation was specific to MRP1 overexpression, as cells upregulating P-glycoprotein accumulated control levels of the probe. Confirmation that SNARF-1 is a MRP1 substrate was obtained using K562 and KG1a cells that have been shown to, respectively, constitutively express MRP1 and P-glycoprotein. Together, the data suggest that SNARF-1 is a substrate for MRP1 but not P-glycoprotein, and could therefore be used as a probe to distinguish between expression and activity of these 2 efflux proteins. Finally, we confirm that doxorubicin but not daunorubicin challenged MRP1 overexpressing HL-60 cells have elevated cytosolic pH.

摘要

细胞功能依赖于细胞内pH值的严格调控,大量报告显示癌细胞的细胞质和细胞器(如溶酶体)具有异常的pH值。5-(及-6)-羧基 seminaphthorhodafluor(SNARF-1)是一种常用的pH敏感探针,在此用于测定HL-60白血病细胞和过表达多药耐药相关蛋白1(MRP1)的耐药变体的细胞质pH值。与亲代细胞相比,耐药细胞积累的SNARF-1明显减少,但通过用特异性MRP1抑制剂MK571预孵育细胞,观察到探针积累接近对照水平。在暴露于阿霉素或柔红霉素后产生了两种新的耐药细胞系,它们分别上调了MRP1或P-糖蛋白的表达。在这些细胞中的实验表明,SNARF-1积累减少是MRP1过表达所特有的,因为上调P-糖蛋白的细胞积累了对照水平的探针。使用已显示分别组成性表达MRP1和P-糖蛋白的K562和KG1a细胞,证实了SNARF-1是MRP1的底物。总之,数据表明SNARF-1是MRP1而非P-糖蛋白的底物,因此可用作区分这两种外排蛋白的表达和活性的探针。最后,我们证实阿霉素而非柔红霉素刺激过表达MRP1的HL-60细胞会使细胞质pH值升高。

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