Mannermaa Eliisa, Vellonen Kati-Sisko, Ryhänen Tuomas, Kokkonen Katriina, Ranta Veli-Pekka, Kaarniranta Kai, Urtti Arto
Department of Pharmaceutics, University of Kuopio, Yliopistonranta 1C, 70210 Kuopio, Finland.
Pharm Res. 2009 Jul;26(7):1785-91. doi: 10.1007/s11095-009-9890-6. Epub 2009 Apr 21.
The objective of this study was to characterize efflux proteins (P-glycoprotein (P-gp), multidrug resistance proteins (MRP1-6) and breast cancer resistance protein (BCRP)) of retinal pigment epithelium (RPE) cell lines.
Expression of efflux proteins in two secondary (ARPE-19, D407) and two primary (HRPEpiC and bovine) RPE cell lines was measured by quantitative RT-PCR and western blotting. Furthermore, activity of MRP1 and MRP5 of ARPE-19 cell line was assessed with calcein-AM and carboxydichlorofluorescein (CDCF) probes.
Similar efflux protein profile was shared between ARPE-19 and primary RPE cells, whereas D407 cell line was notably different. D407 cells expressed MRP2 and BCRP, which were absent in other cell lines and furthermore higher MRP3 transcript expression was found. MRP1, MRP4 and MRP5 were identified from all human RPE cell lines and MRP6 was not expressed in any cell lines. The pattern of efflux protein expression did not change when ARPE-19 cells were differentiated on filters. The calcein-AM and CDCF efflux tests provided evidence supporting MRP1 and MRP5 activity in ARPE-19 cells.
MRP1, MRP4 and MRP5 are the main efflux transporters in RPE cell lines. There are differences in efflux protein expression between RPE cell lines.
本研究的目的是对视网膜色素上皮(RPE)细胞系的外排蛋白(P-糖蛋白(P-gp)、多药耐药蛋白(MRP1-6)和乳腺癌耐药蛋白(BCRP))进行表征。
通过定量逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测两种传代(ARPE-19、D407)和两种原代(HRPEpiC和牛)RPE细胞系中外排蛋白的表达。此外,用钙黄绿素-AM和羧基二氯荧光素(CDCF)探针评估ARPE-19细胞系中MRP1和MRP5的活性。
ARPE-19细胞系和原代RPE细胞具有相似的外排蛋白谱,而D407细胞系明显不同。D407细胞表达MRP2和BCRP,这在其他细胞系中不存在,并且还发现其MRP3转录本表达更高。在所有人类RPE细胞系中均鉴定出MRP1、MRP4和MRP5,而MRP6在任何细胞系中均未表达。当ARPE-19细胞在滤器上分化时,外排蛋白表达模式没有改变。钙黄绿素-AM和CDCF外排试验提供了支持ARPE-19细胞中MRP1和MRP5活性的证据。
MRP1、MRP4和MRP5是RPE细胞系中的主要外排转运蛋白。RPE细胞系之间外排蛋白表达存在差异。