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Am J Physiol Cell Physiol 293: C738-C748, 2007. First published July 25, 2007; doi:10.1152/ajpcell.00157.2007
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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS

Interactions of transmembrane carbonic anhydrase, CAIX, with bicarbonate transporters

Patricio E. Morgan,1 Silvia Pastoreková,2 Alan K. Stuart-Tilley,3 Seth L. Alper,3 and Joseph R. Casey1

1Membrane Protein Research Group, Department of Physiology and Department of Biochemistry, University of Alberta, Edmonton, Alberta, Canada; 2Centre of Molecular Medicine, Institute of Virology, Slovak Academy of Sciences, Bratislava, Slovak Republic; and 3Molecular and Vascular Medicine and Renal Units, Beth Israel Deaconess Medical Center, and the Department of Medicine, Harvard Medical School, Boston, Massachusetts

Submitted 16 April 2007 ; accepted in final form 29 May 2007

Association of some plasma membrane bicarbonate transporters with carbonic anhydrase enzymes forms a bicarbonate transport metabolon to facilitate metabolic CO2-HCO3 conversions and coupled HCO3 transport. The transmembrane carbonic anhydrase, CAIX, with its extracellular catalytic site, is highly expressed in parietal and other cells of gastric mucosa, suggesting a role in acid secretion. We examined in transfected HEK293 cells the functional and physical interactions between CAIX and the parietal cell Cl/HCO3 exchanger AE2 or the putative Cl/HCO3 exchanger SLC26A7. Coexpression of CAIX increased AE2 transport activity by 28 ± 7% and also activated transport mediated by AE1 and AE3 (32 ± 10 and 37 ± 9%, respectively). In contrast, despite a transport rate comparable to that of AE3, coexpressed CAIX did not alter transport associated with SLC26A7. The CAIX-associated increase of AE2 activity did not result from altered AE2 expression or cell surface processing. CAIX was coimmunoprecipitated with the coexpressed SLC4 polypeptides AE1, AE2, and AE3, but not with SLC26A7. GST pull-down assays with a series of domain-deleted forms of CAIX revealed that the catalytic domain of CAIX mediated interaction with AE2. AE2 and CAIX colocalized in human gastric mucosa, as indicated by coimmunofluorescence. This is the first example of a functional and physical interaction between a bicarbonate transporter and a transmembrane carbonic anhydrase. We conclude that CAIX can bind to some Cl/HCO3 exchangers to form a bicarbonate transport metabolon.

SLC4; SLC26; bicarbonate transport metabolon



Address for reprint requests and other correspondence: J. R. Casey, Dept. of Physiology, Univ. of Alberta, Edmonton, Alberta, Canada T6G 2H7 (e-mail: joe.casey{at}ualberta.ca)




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