The breast cancer resistance protein transporter ABCG2 is expressed in the human kidney proximal tubule apical membrane

被引:212
作者
Huls, M. [1 ]
Brown, C. D. A. [2 ]
Windass, A. S. [2 ]
Sayer, R. [2 ]
van den Heuvel, J. J. M. W. [1 ]
Heemskerk, S. [1 ]
Russel, F. G. M. [1 ]
Masereeuw, R. [1 ]
机构
[1] Radboud Univ Nijmegen Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Pharmacol & Toxicol, NL-6500 HB Nijmegen, Netherlands
[2] Univ Newcastle, Sch Med, Inst Cell & Mol Biosci, Newcastle Upon Tyne, Tyne & Wear, England
关键词
ABC transporter; cell and transport physiology; drug excretion; immunostaining;
D O I
10.1038/sj.ki.5002645
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The Breast Cancer Resistance Protein (BCRP/ABCG2) is a transporter restricting absorption and enhancing excretion of many compounds including anticancer drugs. This transporter is highly expressed in many tissues; however, in human kidney, only the mRNA was found in contrast to the mouse kidney, where the transporter is abundant. In bcrp/abcg2((-/-)) mice, the expression of two sterol transporter genes, abcg5 and abcg8, was strongly increased in the kidney, perhaps as a compensatory mechanism to upregulate efflux. We found using immunohistochemical analysis clear localization of BCRP/ABCG2 to the proximal tubule brush border membrane of the human kidney comparable to that of other ABC transporters such as P-glycoprotein/ABCB1, MRP2/ABCC2, and MRP4/ABCC4. Hoechst 33342 dye efflux from primary human proximal tubule cells was significantly reduced by the BCRP/ABCG2 inhibitors fumitremorgin C and nelfinavir. Our study shows that in addition to other apical ABC transporters, BCRP/ABCG2 may be important in renal drug excretion.
引用
收藏
页码:220 / 225
页数:6
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