The stoichiometry of the electrogenic sodium bicarbonate cotransporter NBC1 is cell‐type dependent
- 1 March 2001
- journal article
- Published by Wiley in The Journal of Physiology
- Vol. 531 (3) , 597-603
- https://doi.org/10.1111/j.1469-7793.2001.0597h.x
Abstract
1. The pancreatic variant of the sodium bicarbonate cotransporter, pNBC1, mediates basolateral bicarbonate influx in the exocrine pancreas by coupling the transport of bicarbonate to that of sodium, with a 2 HCO3-:1 Na+ stoichiometry. The kidney variant, kNBC1, mediates basolateral bicarbonate efflux in the proximal tubule by coupling the transport of 3 HCO3- to 1 Na+. The molecular basis underlying the different stoichiometries is not known. 2. pNBC1 and kNBC1 are 93 % identical to each other with 41 N-terminal amino acids of kNBC1 replaced by 85 distinct amino acids in pNBC1. In this study we tested the hypothesis that the differences in stoichiometry are related to the difference between the N-termini of the two proteins. 3. Mouse renal proximal tubule and collecting duct cells, deficient in both pNBC1- and kNBC1-mediated electrogenic sodium bicarbonate cotransport function were transfected with either pNBC1 or kNBC1. Cells were grown on a permeable support to confluence, mounted in an Ussing chamber and permeabilized apically with amphotericin B. Current through the cotransporter was isolated as the difference current due to the reversible inhibitor dinitrostilbene disulfonate. The stoichiometry was calculated from the reversal potential by measuring the current-voltage relationships of the cotransporter at different Na+ concentration gradients. 4. Our data indicate that both kNBC1 and pNBC1 can exhibit either a 2:1 or 3:1 stoichiometry depending on the cell type in which each is expressed. In proximal tubule cells, both pNBC1 and kNBC1 exhibit a 3 HCO3-:1 Na+ stoichiometry, whereas in collecting duct cells, they have a 2:1 stoichiometry. These data argue against the hypothesis that the stoichiometric differences are related to the difference between the N-termini of the two proteins. Moreover, the results suggest that as yet unidentified cellular factor(s) may modify the stoichiometry of these cotransporters.Keywords
This publication has 21 references indexed in Scilit:
- The stoichiometry of the electrogenic sodium bicarbonate cotransporter pNBC1 in mouse pancreatic duct cells is 2 HCO3−:1 Na+The Journal of Physiology, 2001
- Dopamine inhibits renal Na+:HCO3- cotransporter in rabbits and normotensive rats but not in spontaneously hypertensive ratsKidney International, 2000
- Effects of pH on Kinetic Parameters of the Na-HCO3 Cotransporter in Renal Proximal TubuleBiophysical Journal, 1999
- Partial recovery of in vivo function by improved incubation conditions of isolated renal proximal tubulePflügers Archiv - European Journal of Physiology, 1997
- Expression cloning and characterization of a renal electrogenic Na+ /HCO3− cotransporterNature, 1997
- Accumulation of intracellular HCO3‐ by Na(+)‐HCO3‐ cotransport in interlobular ducts from guinea‐pig pancreas.The Journal of Physiology, 1996
- Immortalization and characterization of proximal tubule cells derived from kidneys of spontaneously hypertensive and normotensive ratsKidney International, 1996
- Secretin causes H+/HCO3− secretion from pig pancreatic ductules by vacuolar-type H+-adenosine triphosphataseGastroenterology, 1995
- Membrane localization of H+ and HCO3- transporters in the rat pancreatic duct.The Journal of general physiology, 1994
- Direct derivation of conditionally immortal cell lines from an H-2Kb-tsA58 transgenic mouse.Proceedings of the National Academy of Sciences, 1991