Co-localization and interaction of organic anion transporter 1 with caveolin-2 in rat kidney.
- Author:
Jin Oh KWAK
1
;
Hyun Woo KIM
;
Kwang Jin OH
;
Dong Su KIM
;
Ki Ok HAN
;
Seok Ho CHA
Author Information
1. Department of Pharmacology and Toxicology College of Medicine, Inha University Incheon 400-712, Korea. shcha@inha.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
antisense oligodeoxynucleotide (ODN);
caveolin-2 (Cav-2);
organic anion transporter 1 (OAT1);
renal proximal tubule
- MeSH:
Animals;
Biological Transport, Active/*physiology;
CHO Cells;
Caveolins/*metabolism;
Cell Membrane/*metabolism;
Cells, Cultured;
Hamsters;
Immunoprecipitation;
Kidney Tubules, Proximal/*metabolism;
Methotrexate/metabolism;
Microscopy, Confocal;
Oligonucleotides, Antisense/pharmacology;
Oocytes/metabolism;
Organic Anion Transport Protein 1/antagonists & inhibitors/genetics/*metabolism;
RNA, Complementary/metabolism;
RNA, Messenger/genetics/metabolism;
Rats;
Research Support, Non-U.S. Gov't;
Xenopus laevis/metabolism;
p-Aminohippuric Acid/metabolism
- From:Experimental & Molecular Medicine
2005;37(3):204-212
- CountryRepublic of Korea
- Language:English
-
Abstract:
The organic anion transporters (OAT) have recently been identified. Although the some transport properties of OATs in the kidney have been verified, the regulatory mechanisms for OAT's functions are still not fully understood. The rat OAT1 (rOAT1) transports a number of negatively charged organic compounds between the cells and their extracellular milieu. Caveolin (Cav) also plays a role in membrane transport. Therefore, we investigated the protein-protein interactions between rOAT1 and caveolin-2. In the rat kidney, the expressions of rOAT1 mRNA and protein were observed in both the cortex and the outer medulla. With respect to Cav-2, the expressions of mRNA and protein were observed in all portions of the kidney (cortex < outer medulla = inner medulla). The results of Western blot analysis using the isolated caveolae-enriched membrane fractions or the immunoprecipitates by respective antibodies from the rat kidney showed that rOAT1 and Cav-2 co-localized in the same fractions and they formed complexes each other. These results were confirmed by performing confocal microscopy with immunocytochemistry using the primary cultured renal proximal tubular cells. When the synthesized cRNA of rOAT1 along with the antisense oligodeoxynucleotides of Xenopus Cav-2 were co-injected into Xenopus oocytes, the [14C]p-aminohippurate and [3H]methotrexate uptake was slightly, but significantly decreased. The similar results were also observed in rOAT1 over-expressed Chinese hamster ovary cells. These findings suggest that rOAT1 and caveolin-2 are co-expressed in the plasma membrane and rOAT1's function for organic compound transport is upregulated by Cav-2 in the normal physiological condition.
