Literature DB >> 11230510

The stoichiometry of the electrogenic sodium bicarbonate cotransporter pNBC1 in mouse pancreatic duct cells is 2 HCO(3)(-):1 Na(+).

E Gross1, N Abuladze, A Pushkin, I Kurtz, C U Cotton.   

Abstract

The electrogenic sodium bicarbonate cotransporter pNBC1 is believed to play a major role in the secretion of bicarbonate by pancreatic duct cells, by transporting bicarbonate into the cell across the basolateral membrane. Thermodynamics predict that this function can be achieved only if the reversal potential of the cotransporter is negative to the cell's membrane potential, or equivalently that the HCO3-:Na+ stoichiometry is not larger then 2:However, there are no data available on either the reversal potential or the HCO3-:Na+ stoichiometry of pNBC1 in pancreatic cells. We studied pNBC1 function in mouse pancreatic duct cells. RT-PCR analysis of total RNA revealed that these cells contain the message for pNBC1, but not for kNBC1, NBC2 or NBC3. To measure cotransporter activity, mouse pancreatic duct cells were grown to confluence on a porous substrate, mounted in an Ussing chamber, and the apical plasma membrane permeabilized with amphotericin B. Ion flux through pNBC1 was achieved by applying Na+ concentration gradients across the basolateral plasma membrane. The current through the cotransporter was isolated as the difference current due to the reversible inhibitor dinitrostilbene disulfonate (DNDS). Current-voltage relationships for the cotransporter, measured at three different Na+ concentration gradients, were linear over a range of about 100 mV. The reversal potential data, obtained from these current-voltage relationships, all corresponded to a 2 HCO3-:1 Na+ stoichiometry. The data indicate that pNBC1 is functionally expressed in mouse pancreatic duct cells. The cotransporter operates with a 2 HCO3-:1 Na+ stoichiometry in these cells, and mediates the transport of bicarbonate into the cell across the basolateral membrane.

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Year:  2001        PMID: 11230510      PMCID: PMC2278477          DOI: 10.1111/j.1469-7793.2001.0375i.x

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  42 in total

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4.  Activity and stoichiometry of Na+:HCO3- cotransport in immortalized renal proximal tubule cells.

Authors:  E Gross; U Hopfer
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5.  Secretin causes H+/HCO3- secretion from pig pancreatic ductules by vacuolar-type H(+)-adenosine triphosphatase.

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6.  Effect of secretin and inhibitors of HCO3-/H+ transport on the membrane voltage of rat pancreatic duct cells.

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Journal:  Pflugers Arch       Date:  1993-11       Impact factor: 3.657

7.  Micropuncture study of pancreatic secretion in the cat.

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9.  Effect of acetyl choline on ion transport in sheep tracheal epithelium.

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10.  Membrane localization of H+ and HCO3- transporters in the rat pancreatic duct.

Authors:  H Zhao; R A Star; S Muallem
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  23 in total

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Review 2.  Molecular mechanisms of electrogenic sodium bicarbonate cotransport: structural and equilibrium thermodynamic considerations.

Authors:  I Kurtz; D Petrasek; S Tatishchev
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3.  Entry to "formula tunnel" revealed by SLC4A4 human mutation and structural model.

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4.  Role of an extracellular loop in determining the stoichiometry of Na+-HCO₃⁻ cotransporters.

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Journal:  J Physiol       Date:  2011-01-04       Impact factor: 5.182

Review 5.  The divergence, actions, roles, and relatives of sodium-coupled bicarbonate transporters.

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Journal:  Physiol Rev       Date:  2013-04       Impact factor: 37.312

Review 6.  NBCe1 as a model carrier for understanding the structure-function properties of Na⁺ -coupled SLC4 transporters in health and disease.

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7.  Phosphorylation-induced modulation of pNBC1 function: distinct roles for the amino- and carboxy-termini.

Authors:  E Gross; O Fedotoff; A Pushkin; N Abuladze; D Newman; I Kurtz
Journal:  J Physiol       Date:  2003-05-02       Impact factor: 5.182

Review 8.  Modular structure of sodium-coupled bicarbonate transporters.

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9.  PKC{alpha}{beta}{gamma}- and PKC{delta}-dependent endocytosis of NBCe1-A and NBCe1-B in salivary parotid acinar cells.

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