Literature DB >> 8444418

Accumulation of organic anion in intracellular vesicles of cultured rat hepatocytes is mediated by the canalicular multispecific organic anion transporter.

R P Oude Elferink1, C T Bakker, H Roelofsen, E Middelkoop, R Ottenhoff, M Heijn, P L Jansen.   

Abstract

Transport of organic anions within hepatocytes and the possible involvement of intracellular vesicles were studied with fluorescence microscopy. For this purpose monochlorobimane, a nonfluorescent hydrophobic compound that readily permeates into cells and is conjugated with glutathione to form the fluorescent glutathione bimane, was used. In the isolated perfused livers of normal rats, glutathione bimane is rapidly secreted into bile. In contrast, in our study of livers from mutant TR- rats, a 100-fold reduction in glutathione bimane secretion into bile occurred. Mutant TR- rats have an inherited defect in the canalicular multispecific organic anion transporter, which mediates the ATP-dependent secretion of a wide range of organic anions over the canalicular membrane into bile. When cultured Wistar and TR- hepatocytes were loaded with glutathione bimane, both cell types displayed a strong cytosolic fluorescence. Wistar cells completely lost this cytosolic fluorescence at incubation on monochlorobimane-free medium because of secretion of glutathione bimane. A clear punctate fluorescence remained, however, which was scattered through the cell with some perinuclear concentration. In some cells vesicular fluorescence was also concentrated around a canaliculus. In contrast, TR- cells lost their cytosolic fluorescence more slowly and completely lacked the vesicular fluorescence. Making cells selectively permeable with digitonin directly after loading them with glutathione bimane to remove cytosolic fluorescence again revealed the presence of fluorescent vesicles in Wistar cells and their absence in TR- cells. In Wistar cells vesicular fluorescence could be increased by preincubation with monensin or methylamine, compounds that have been shown to interfere with plasma membrane recycling. In conclusion, these results suggest that apart from secretion over the plasma membrane, the canalicular multispecific organic anion transporter may be involved in accumulation of organic anion in intracellular vesicles. It is hypothesized that this intracellular localization of the canalicular multispecific organic anion transporter is caused by recycling of the transporter between the plasma membrane and intracellular membranes.

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Year:  1993        PMID: 8444418

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  9 in total

1.  Transfected rat cMOAT is functionally expressed on the apical membrane in Madin-Darby canine kidney (MDCK) cells.

Authors:  S Kinoshita; H Suzuki; K Ito; K Kume; T Shimizu; Y Sugiyama
Journal:  Pharm Res       Date:  1998-12       Impact factor: 4.200

2.  Modifying hepatic phospholipid synthesis associates with biliary phospholipid secretion rate in a transporter-independent manner in rats: relation to canalicular membrane fluidity.

Authors:  S Yasumiba; S Tazuma; H Ochi; G Kajiyama
Journal:  Dig Dis Sci       Date:  2001-06       Impact factor: 3.199

3.  Role of multidrug resistance protein 2 (MRP2) in glutathione-bimane efflux from Caco-2 and rat renal proximal tubule cells.

Authors:  S A Terlouw; R Masereeuw; P H van den Broek; S Notenboom; F G Russel
Journal:  Br J Pharmacol       Date:  2001-11       Impact factor: 8.739

4.  Regulation of multidrug resistance-associated protein 2 by calcium signaling in mouse liver.

Authors:  Laura N Cruz; Mateus T Guerra; Emma Kruglov; Albert Mennone; Celia R S Garcia; Ju Chen; Michael H Nathanson
Journal:  Hepatology       Date:  2010-07       Impact factor: 17.425

5.  Localization of P-gp (Abcb1) and Mrp2 (Abcc2) in freshly isolated rat hepatocytes.

Authors:  Daniel A J Bow; Jennifer L Perry; David S Miller; John B Pritchard; Kim L R Brouwer
Journal:  Drug Metab Dispos       Date:  2007-10-22       Impact factor: 3.922

6.  Partial characterization of mechanisms of cytoprotective action of hydrophilic bile salts against hydrophobic bile salts in rats: relation to canalicular membrane fluidity and packing density.

Authors:  H Miyake; S Tazuma; H Miura; G Yamashita; G Kajiyama
Journal:  Dig Dis Sci       Date:  1999-01       Impact factor: 3.199

Review 7.  The complexities of hepatic drug transport: current knowledge and emerging concepts.

Authors:  Priyamvada Chandra; Kim L R Brouwer
Journal:  Pharm Res       Date:  2004-05       Impact factor: 4.580

8.  In vivo cisplatin resistance depending upon canalicular multispecific organic anion transporter (cMOAT).

Authors:  T Minamino; M Tamai; Y Itoh; Y Tatsumi; M Nomura; K Yokogawa; H Suzuki; Y Sugiyama; T Ohshima; K Miyamoto
Journal:  Jpn J Cancer Res       Date:  1999-10

Review 9.  Regulation of organic anion transport in the liver.

Authors:  H Roelofsen; M Müller; P L Jansen
Journal:  Yale J Biol Med       Date:  1997 Jul-Aug
  9 in total

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