Localization of organic cation transporters OCT1 and OCT2 in rat kidney

2000 ◽  
Vol 279 (4) ◽  
pp. F679-F687 ◽  
Author(s):  
Ulrich Karbach ◽  
Jörn Kricke ◽  
Friederike Meyer-Wentrup ◽  
Valentin Gorboulev ◽  
Christopher Volk ◽  
...  

Renal excretion and reabsorption of organic cations are mediated by electrogenic and electroneutral organic cation transporters, which belong to a recently discovered family of polyspecific transporters. These transporters are electrogenic and exhibit differences in substrate specificity. In rat, the renal expression of the polyspecific cation transporters rOCT1 and rOCT2 was investigated. By in situ hybridization, significant amounts of both rOCT1 and rOCT2 mRNA were detected in S1, S2, and S3 segments of proximal tubules. By immunohistochemistry, expression of the rOCT1 protein was mainly observed in S1 and S2 segments of proximal tubules, with lower expression levels in the S3 segments. At variance, rOCT2 protein was mainly expressed in the S2 and S3 segments. Both transporters were localized to the basolateral cell membrane. Neither rOCT1 nor rOCT2 was detected in the vasculature, the glomeruli, and nephron segments other than proximal tubules. The data suggest that rOCT1 and rOCT2 are responsible for basolateral cation uptake in the proximal tubule, which represents the first step in cation secretion.

2009 ◽  
Vol 296 (6) ◽  
pp. F1504-F1513 ◽  
Author(s):  
Wing-Kee Lee ◽  
Markus Reichold ◽  
Bayram Edemir ◽  
Giuliano Ciarimboli ◽  
Richard Warth ◽  
...  

The positively charged fluorescent dyes ethidium (Et+) and propidium (Pr2+) are widely used as DNA and necrosis markers. Et+is cytotoxic and mutagenic. The polyspecific organic cation transporters OCT1 (SLC22A1), OCT2 (SLC22A2), and OCT3 (SLC22A3) mediate electrogenic facilitated diffusion of small (≤500 Da) organic cations with broad specificities. In humans, OCT2 mediates basolateral uptake by kidney proximal tubules (PT), whereas in rodents OCT1/2 are involved. In mouse kidney, perfused Et+accumulated predominantly in the S2/S3 segments of the PT, but not Pr2+. In cells stably overexpressing human OCTs (hOCTs), Et+uptake was observed with Kmvalues of 0.8 ± 0.2 μM (hOCT1), 1.7 ± 0.5 μM (hOCT2), and 2.0 ± 0.5 μM (hOCT3), whereas Pr2+was not transported. Accumulation of Et+was inhibited by OCT substrates quinine, 3-methyl-4-phenylpyridinium (MPP+), cimetidine, and tetraethylammonium (TEA+). For hOCT1 and hOCT2, the IC50values for MPP+, TEA+, and cimetidine were higher than for inhibition of previously tested transported substrates. For hOCT2, the inhibition of Et+uptake by MPP+and cimetidine was shown to be competitive. Et+also inhibited transport of 0.1 μM [3H]MPP+by all hOCT isoforms with IC50values between 0.4 and 1.3 μM, and the inhibition of hOCT1-mediated uptake of MPP+by Et+was competitive. In Oct1/2−/−mice, Et+uptake in the PT was almost abolished. The data demonstrate that Et+is taken up avidly by the PT, which is mediated by OCT1 and/or OCT2. Considering the high affinity of OCTs for Et+and their strong expression in various organs, strict safety guidelines for Et+handling should be reinforced.


2008 ◽  
Vol 584 (2-3) ◽  
pp. 390-397 ◽  
Author(s):  
Suzanne Heemskerk ◽  
Alfons C. Wouterse ◽  
Frans G.M. Russel ◽  
Rosalinde Masereeuw

2008 ◽  
Vol 37 (2) ◽  
pp. 424-430 ◽  
Author(s):  
Xin Ming ◽  
Wujian Ju ◽  
Huali Wu ◽  
Richard R. Tidwell ◽  
James E. Hall ◽  
...  

2013 ◽  
Vol 116 ◽  
pp. 27-35 ◽  
Author(s):  
Jayabalan Nirmal ◽  
Anju Sirohiwal ◽  
Sundararajan Baskar Singh ◽  
Nihar Ranjan Biswas ◽  
Vasantha Thavaraj ◽  
...  

2010 ◽  
Vol 39 (1-3) ◽  
pp. 76-81 ◽  
Author(s):  
Kristiina Tertti ◽  
Ulla Ekblad ◽  
Tuija Heikkinen ◽  
Melissa Rahi ◽  
Tapani Rönnemaa ◽  
...  

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