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

Autor: Suzanne Heemskerk, Rachel Sayer, Colin D.A. Brown, Miriam Huls, Amy S. Windass, Rosalinde Masereeuw, Frans G. M. Russel, J. J. M. W. van den Heuvel
Rok vydání: 2008
Předmět:
medicine.medical_specialty
animal structures
Abcg2
Membrane transport and intracellular motility [NCMLS 5]
cell and transport physiology
ATP-binding cassette transporter
Synthetic Organic Chemistry
ABCC4
Polymerase Chain Reaction
Kidney Tubules
Proximal

Metabolism
transport and motion [NCMLS 2]

Mice
Internal medicine
medicine
ATP Binding Cassette Transporter
Subfamily G
Member 2

Animals
Humans
RNA
Messenger

Renal disorder [IGMD 9]
immunostaining
Kidney
biology
Multidrug resistance-associated protein 2
Cell Membrane
Transporter
Apical membrane
Immunohistochemistry
Molecular biology
Multidrug Resistance-Associated Protein 2
Neoplasm Proteins
Rats
Renal disorders [UMCN 5.4]
medicine.anatomical_structure
Endocrinology
drug excretion
Nephrology
biology.protein
ATP-Binding Cassette Transporters
ABC transporter
Efflux
Zdroj: Kidney International. Supplement, 73, 220-5
Kidney International. Supplement, 73, 2, pp. 220-5
ISSN: 0085-2538
2157-1724
DOI: 10.1038/sj.ki.5002645
Popis: Contains fulltext : 70782.pdf (Publisher’s version ) (Closed access) 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.
Databáze: OpenAIRE