Literature DB >> 11912243

Immunolocalization of multispecific organic anion transporters, OAT1, OAT2, and OAT3, in rat kidney.

Ryoji Kojima1, Takashi Sekine1, Masanao Kawachi1, Seok Ho Cha1, Yoshio Suzuki1, Hitoshi Endou1.   

Abstract

Recently, a family of multispecific organic anion transporters has been identified, and several isoforms have been reported. However, the physiologic and pharmacologic roles of each isoform, except OAT1, in the transepithelial transport of organic anions in the kidney remain to be elucidated. To address this issue, it is essential to determine the intrarenal distribution and membrane localization of each OAT isoform along the nephron. In this study, the intrarenal distributions of rOAT1, rOAT2, and rOAT3 were investigated by an immunofluorescence method that used frozen rat serial kidney sections. Confocal microscopic analysis showed that immunoreactivity for rOAT1 was detected exclusively in the proximal tubules (S1, S2, S3) in the cortex with basolateral membrane staining. rOAT2 was detected in the apical surface of the tubules in the medullary thick ascending limb of Henle's loop (MTAL) and cortical and medullary collecting ducts (CD). rOAT3 was localized in the basolateral digitation of the cell membrane in all the segments (S1, S2, and S3) of the proximal tubules, MTAL, cortical TAL, connecting tubules, and cortical and medullary CD. These results on the distribution of each OAT isoform will facilitate the understanding of the role of OATs in the renal processing of organic anions.

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Year:  2002        PMID: 11912243     DOI: 10.1681/ASN.V134848

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  45 in total

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2.  Prominin-2 is a novel marker of distal tubules and collecting ducts of the human and murine kidney.

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Review 3.  Organic anion transporters of the SLC22 family: biopharmaceutical, physiological, and pathological roles.

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Journal:  Pharm Res       Date:  2007-03       Impact factor: 4.200

Review 4.  Global analysis of gene expression in mammalian kidney.

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Journal:  Pflugers Arch       Date:  2004-12-21       Impact factor: 3.657

5.  Functional maturation of drug transporters in the developing, neonatal, and postnatal kidney.

Authors:  Derina E Sweeney; Volker Vallon; Timo Rieg; Wei Wu; Thomas F Gallegos; Sanjay K Nigam
Journal:  Mol Pharmacol       Date:  2011-04-14       Impact factor: 4.436

6.  Renal elimination of organic anions in cholestasis.

Authors:  Adriana Monica Torres
Journal:  World J Gastroenterol       Date:  2008-11-21       Impact factor: 5.742

Review 7.  The organic anion transporter (OAT) family: a systems biology perspective.

Authors:  Sanjay K Nigam; Kevin T Bush; Gleb Martovetsky; Sun-Young Ahn; Henry C Liu; Erin Richard; Vibha Bhatnagar; Wei Wu
Journal:  Physiol Rev       Date:  2015-01       Impact factor: 37.312

8.  Sex-dependent expression of Oat3 (Slc22a8) and Oat1 (Slc22a6) proteins in murine kidneys.

Authors:  Davorka Breljak; Hrvoje Brzica; Douglas H Sweet; Naohiko Anzai; Ivan Sabolic
Journal:  Am J Physiol Renal Physiol       Date:  2013-02-06

Review 9.  Toward a systems level understanding of organic anion and other multispecific drug transporters: a remote sensing and signaling hypothesis.

Authors:  Sun-Young Ahn; Sanjay K Nigam
Journal:  Mol Pharmacol       Date:  2009-06-10       Impact factor: 4.436

10.  Regulation of renal organic anion transporter 3 (SLC22A8) expression and function by the integrity of lipid raft domains and their associated cytoskeleton.

Authors:  Chutima Srimaroeng; Jennifer Perry Cecile; Ramsey Walden; John B Pritchard
Journal:  Cell Physiol Biochem       Date:  2013-04-26
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