Slc26a9—Anion Exchanger, Channel and Na+ Transporter
- 14 April 2009
- journal article
- research article
- Published by Springer Nature in The Journal of Membrane Biology
- Vol. 228 (3), 125-140
- https://doi.org/10.1007/s00232-009-9165-5
Abstract
The SLC26 gene family encodes anion transporters with diverse functional attributes: (a) anion exchanger, (b) anion sensor, and (c) anion conductance (likely channel). We have cloned and studied Slc26a9, a paralogue expressed mostly in lung and stomach. Immunohistochemistry shows that Slc26a9 is present at apical and intracellular membranes of lung and stomach epithelia. Using expression in Xenopus laevis oocytes and ion-sensitive microelectrodes, we discovered that Slc26a9 has a novel function not found in any other Slc26 proteins: cation coupling. Intracellular pH and voltage measurements show that Slc26a9 is a nCl−-HCO −3 exchanger, suggesting roles in gastric HCl secretion or pulmonary HCO −3 secretion; Na+ electrodes and uptakes reveal that Slc26a9 has a cation dependence. Single-channel measurements indicate that Slc26a9 displays discrete open and closed states. These experiments show that Slc26a9 has three discrete physiological modes: nCl−-HCO −3 exchanger, Cl− channel, and Na+-anion cotransporter. Thus, the Slc26a9 transporter channel is uniquely suited for dynamic and tissue-specific physiology or regulation in epithelial tissues.Keywords
This publication has 61 references indexed in Scilit:
- Deletion of the chloride transporter Slc26a9 causes loss of tubulovesicles in parietal cells and impairs acid secretion in the stomachProceedings of the National Academy of Sciences, 2008
- SLC26A9 is a Cl− channel regulated by the WNK kinasesThe Journal of Physiology, 2007
- Coupling Modes and Stoichiometry of Cl−/HCO3− Exchange by slc26a3 and slc26a6The Journal of general physiology, 2006
- Secondary active transport mediated by a prokaryotic homologue of ClC Cl- channelsNature, 2004
- Molecular characterization of the murine Slc26a6 anion exchanger: functional comparison with Slc26a1American Journal of Physiology-Renal Physiology, 2002
- Regulatory Interaction between the Cystic Fibrosis Transmembrane Conductance Regulator and HCO Salvage Mechanisms in Model Systems and the Mouse Pancreatic DuctJournal of Biological Chemistry, 2001
- Cloning, Characterization, and Chromosomal Mapping of a Human Electroneutral Na+-driven Cl-HCO3ExchangerPublished by Elsevier ,2001
- Cloning and Characterization of a Na+-driven Anion Exchanger (NDAE1)Journal of Biological Chemistry, 2000
- Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)Nature Genetics, 1997
- Sulfate Transport in Chondrodysplasia,aAnnals of the New York Academy of Sciences, 1996