Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
Enhanced secretion of glycocholic acid in a specially adapted cell line is associated with overexpression of apparently novel ATP-binding cassette proteins.
Brown RS
,
Lomri N
,
De Voss J
,
Rahmaoui CM
,
Xie MH
,
Hua T
,
Lidofsky SD
,
Scharschmidt BF
.
???displayArticle.abstract???
Secretion of anionic endo- and xenobiotics is essential for the survival of animal and plant cells; however, the underlying molecular mechanisms remain uncertain. To better understand one such model system--i.e., secretion of bile acids by the liver--we utilized a strategy analogous to that employed to identify the multidrug resistance (mdr) genes. We synthesized the methyl ester of glycocholic acid (GCE), which readily enters cells, where it is hydrolyzed to yield glycocholic acid, a naturally occurring bile acid. The rat hepatoma-derived HTC cell line gradually acquired resistance to GCE concentrations 20-fold higher than those which inhibited growth of naive cells, yet intracellular accumulation of radiolabel in resistant cells exposed to [14C]GCE averaged approximately 25% of that in nonresistant cells. As compared with nonresistant cells, resistant cells also exhibited (i) cross-resistance to colchicine, a known mdr substrate, but not to other noxious substances transported by hepatocytes; (ii) increased abundance on Northern blot of mRNA species up to 7-10 kb recognized by a probe for highly conserved nucleotide-binding domain (NBD) sequences of ATP-binding cassette (ABC) proteins; (iii) increased abundance, as measured by RNase protection assay, of mRNA fragments homologous to a NBD cRNA probe; and (iv) dramatic overexpression, as measured by Western blotting and immunofluorescence, of a group of 150- to 200-kDa plasma membrane proteins recognized by a monoclonal antibody against a region flanking the highly conserved NBD of mdr/P-glycoproteins. Finally, Xenopus laevis oocytes injected with mRNA from resistant cells and incubated with [14C]GCE secreted radiolabel more rapidly than did control oocytes. Enhanced secretion of glycocholic acid in this cell line is associated with overexpression of ABC/mdr-related proteins, some of which are apparently novel and are likely to include a bile acid transport protein.
Arias,
The biology of the bile canaliculus, 1993.
1993, Pubmed
Arias,
The biology of the bile canaliculus, 1993.
1993,
Pubmed
Becker,
Characterisation of the ATP-dependent taurocholate-carrier protein (gp110) of the hepatocyte canalicular membrane.
1993,
Pubmed
Buschman,
mdr2 encodes P-glycoprotein expressed in the bile canalicular membrane as determined by isoform-specific antibodies.
1992,
Pubmed
Cao,
J774 macrophages secrete antibiotics via organic anion transporters.
1992,
Pubmed
Chin,
Regulation of mdr RNA levels in response to cytotoxic drugs in rodent cells.
1990,
Pubmed
Chomczynski,
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.
1987,
Pubmed
Georges,
Detection of P-glycoprotein isoforms by gene-specific monoclonal antibodies.
1990,
Pubmed
Gottesman,
Biochemistry of multidrug resistance mediated by the multidrug transporter.
1993,
Pubmed
Hediger,
Expression cloning and cDNA sequencing of the Na+/glucose co-transporter.
,
Pubmed
,
Xenbase
Homolya,
Fluorescent cellular indicators are extruded by the multidrug resistance protein.
1993,
Pubmed
Hörtensteiner,
Direct energization of bile acid transport into plant vacuoles.
1993,
Pubmed
Kast,
Hepatocellular transport of bile acids. Evidence for distinct subcellular localizations of electrogenic and ATP-dependent taurocholate transport in rat hepatocytes.
1994,
Pubmed
Kioka,
Heat-shock responsive elements in the induction of the multidrug resistance gene (MDR1).
1992,
Pubmed
Laemmli,
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
1970,
Pubmed
Lin,
Cloning and expression of a cDNA coding for a rat liver plasma membrane ecto-ATPase. The primary structure of the ecto-ATPase is similar to that of the human biliary glycoprotein I.
1989,
Pubmed
LOWRY,
Protein measurement with the Folin phenol reagent.
1951,
Pubmed
Müller,
ATP-dependent transport of taurocholate across the hepatocyte canalicular membrane mediated by a 110-kDa glycoprotein binding ATP and bile salt.
1991,
Pubmed
Rigby,
Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.
1977,
Pubmed
Ruetz,
Phosphatidylcholine translocase: a physiological role for the mdr2 gene.
1994,
Pubmed
Schinkel,
Characterization of the human MDR3 P-glycoprotein and its recognition by P-glycoprotein-specific monoclonal antibodies.
1991,
Pubmed
Shen,
Multiple drug-resistant human KB carcinoma cells independently selected for high-level resistance to colchicine, adriamycin, or vinblastine show changes in expression of specific proteins.
1986,
Pubmed
Shneider,
Characterization of endogenous carrier-mediated taurocholate efflux from Xenopus laevis oocytes.
1993,
Pubmed
,
Xenbase
Sippel,
The rat liver ecto-ATPase is also a canalicular bile acid transport protein.
1993,
Pubmed
Smit,
Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease.
1993,
Pubmed
Tanzi,
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene.
1993,
Pubmed
Towbin,
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
1979,
Pubmed