Evidence for carrier-mediated chloride/bicarbonate exchange in canalicular rat liver plasma membrane vesicles.
Open Access
- 1 April 1985
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 75 (4) , 1256-1263
- https://doi.org/10.1172/jci111824
Abstract
To determine whether anion exchangers might play a role in hepatic bile formation, we looked for the presence of Cl-:OH- and Cl-:HCO3- exchange in highly purified canalicular (c) and basolateral (bl) rat liver plasma membrane (LPM) vesicles. In cLPM vesicles, a pH gradient (7.7 in/6.0 out) stimulated 36Cl- uptake twofold above values obtained during pH-equilibrated conditions (7.7 in = out). When 50 mM HCO3- was also present inside the vesicles, the same pH gradient (7.7 in/6.0 out) resulted in Cl- uptake to levels fourfold above pH- and HCO3--equilibrated controls and two- to threefold above Cl- equilibrium (overshoot). Initial rates of both pH and HCO3- gradient-stimulated Cl- uptake were completely inhibited by 4,4'-diisothiocyano-2,2'-disulfonic acid stilbene (DIDS). A valinomycin-induced K+ diffusion potential (inside positive) also stimulated Cl- uptake in cLPM, but this conductive Cl- pathway was insensitive to DIDS. The DIDS-sensitive, pH and HCO3- gradient-stimulated Cl- uptake demonstrated: saturation with Cl- (Km approximately 6.3 mM; Vmax approximately 51 nmol X mg-1 X min-1); partial inhibition by bumetanide (26%), furosemide (33%), probenecid (37%), and 4-acetamido-4'-isothiocyano-2,2'-disulfonic acid stilbene (49%); cis-inhibition by chloride and nitrate but not by sulfate and various organic anions, and independence from the membrane potential. These data demonstrate the presence of an electroneutral Cl-:OH- and Cl-:HCO3- exchanger in rat liver canalicular membranes that favors Cl-:HCO3- exchange. In contrast, no evidence was found for the presence of a Cl-:HCO3- (OH-) exchange system in blLPM vesicles. Furthermore, neither blLPM nor cLPM vesicles exhibited Na+-stimulatable Cl- uptake, indicating the absence of a NaCl co-transport system in either LPM subfraction. These findings are consistent with a functional role for a Cl-:HCO3- (OH-) exchanger in canalicular bile formation.This publication has 44 references indexed in Scilit:
- Taurocholate transport by rat liver canalicular membrane vesicles. Evidence for the presence of an Na+-independent transport system.Journal of Clinical Investigation, 1984
- Structural and functional polarity of canalicular and basolateral plasma membrane vesicles isolated in high yield from rat liver.The Journal of cell biology, 1984
- Requirement of Cl− and Na+ for the ouabain-resistant control of cell volume in slices of rat liverThe Journal of Membrane Biology, 1984
- Proton transport and cell function.Journal of Clinical Investigation, 1984
- The Activity of Sulfonamides and Anions Against the Carbonic Anhydrases of Animals, Plants, and BacteriaAnnual Review of Pharmacology and Toxicology, 1983
- Membrane transport of anions across epithelia of mammalian small intestine and kidney proximal tubulePublished by Springer Nature ,1983
- Effects of ion substitution on bile acid-dependent and -independent bile formation by rat liver.Journal of Clinical Investigation, 1982
- The anion transport system of the red blood cell The role of membrane protein evaluated by the use of ‘probes’Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1978
- Furosemide inhibition of chloride transport in human red blood cells.The Journal of general physiology, 1976
- The inhibitor effect of probenecid and structural analogues on organic anions and chloride permeabilities in ox erythrocytesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1976