Distribution of organic anion transporters NaDC3 and OAT1-3 along the human nephron

• Published in: American journal of physiology. Renal physiology 2016-07, Vol.311 (1), p.F227-F238
• Main Authors: Breljak, Davorka, Ljubojević, Marija, Hagos, Yohannes, Micek, Vedran, Balen Eror, Daniela, Vrhovac Madunić, Ivana, Brzica, Hrvoje, Karaica, Dean, Radović, Nikola, Kraus, Ognjen, Anzai, Naohiko, Koepsell, Hermann, Burckhardt, Gerhard, Burckhardt, Birgitta C, Sabolić, Ivan
• Format: Article
• Language: English
• Subjects: Adenosine triphosphatase; Adult; Dicarboxylic Acid Transporters - metabolism; Female; HEK293 Cells; Humans; Immunoglobulins; Immunology; Kidney Medulla - metabolism; Kidney Tubules, Collecting - metabolism; Kidney Tubules, Distal - metabolism; Kidneys; Male; Membranes - metabolism; Middle Aged; Nephrology; Nephrons - metabolism; Organic Anion Transport Protein 1 - metabolism; Organic Anion Transporters - metabolism; Organic Anion Transporters, Sodium-Dependent - metabolism; Organic Anion Transporters, Sodium-Independent - metabolism; Physiology; Protein expression; Sex Characteristics; Sodium-Potassium-Exchanging ATPase - metabolism; Symporters - metabolism
• ISSN: 1931-857X; 1522-1466
• DOI: 10.1152/ajprenal.00113.2016

The initial step in renal secretion of organic anions (OAs) is mediated by transporters in the basolateral membrane (BLM). Contributors to this process are primary active Na(+)-K(+)-ATPase (EC 3.6.3.9), secondary active Na(+)-dicarboxylate cotransporter 3 (NaDC3/SLC13A3), and tertiary active OA transporters (OATs) OAT1/SLC22A6, OAT2/SLC22A7, and OAT3/SLC22A8. In human kidneys, we analyzed the localization of these transporters by immunochemical methods in tissue cryosections and isolated membranes. The specificity of antibodies was validated with human embryonic kidney-293 cells stably transfected with functional OATs. Na(+)-K(+)-ATPase was immunolocalized to the BLM along the entire human nephron. NaDC3-related immunostaining was detected in the BLM of proximal tubules and in the BLM and/or luminal membrane of principal cells in connecting segments and collecting ducts. The thin and thick ascending limbs, macula densa, and distal tubules exhibited no reactivity with the anti-NaDC3 antibody. OAT1-OAT3-related immunostaining in human kidneys was detected only in the BLM of cortical proximal tubules; all three OATs were stained more intensely in S1/S2 segments compared with S3 segment in medullary rays, whereas the S3 segment in the outer stripe remained unstained. Expression of NaDC3, OAT1, OAT2, and OAT3 proteins exhibited considerable interindividual variability in both male and female kidneys, and sex differences in their expression could not be detected. Our experiments provide a side-by-side comparison of basolateral transporters cooperating in renal OA secretion in the human kidney.