Journal of Biological Chemistry
Volume 275, Issue 45, 10 November 2000, Pages 35486-35490
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MEMBRANE TRANSPORT STRUCTURE FUNCTION AND BIOGENESIS
The Na+-driven Cl/HCO3Exchanger: CLONING, TISSUE DISTRIBUTION, AND FUNCTIONAL CHARACTERIZATION*210

https://doi.org/10.1074/jbc.C000456200Get rights and content
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The Na+-driven Cl/HCO3exchanger is an important regulator of intracellular pH in various cells, but its molecular basis has not been determined. We show here the primary structure, tissue distribution, and functional characterization of Na+-drivenchloride/bicarbonate exchanger (designated NCBE ) cloned from the insulin-secreting cell line MIN6 cDNA library. The NCBE protein consists of 1088 amino acids having 74, 72, and 55% amino acid identity to the human skeletal muscle, rat smooth muscle, and human kidney sodium bicarbonate cotransporter, respectively. The protein has 10 putative membrane-spanning regions. NCBE mRNA is expressed at high levels in the brain and the mouse insulinoma cell line MIN6 and at low levels in the pituitary, testis, kidney, and ileum. Functional analyses of the NCBE protein expressed inXenopus laevis oocytes and HEK293 cells demonstrate that it transports extracellular Na+ and HCO3 into cells in exchange for intracellular Cl and H+, thus raising the intracellular pH. Thus, we conclude that NCBE is a Na+-driven Cl/HC O3exchanger that regulates intracellular pH in native cells.

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Published, JBC Papers in Press, September 18, 2000, DOI 10.1074/jbc.C000456200

AB033759

*

This work was supported by Grant-in-aid 10NP0201 for Creative Basic Research from the Ministry of Education, Science, Sports and Culture and by grants from the Ministry of Health and Welfare, Japan, Novo Nordisk Pharma Ltd., Yamanouchi Foundation for Research on Metabolic Disorders, and Suzuken Memorial Foundation.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

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The on-line version of this article (available athttp://www.jbc.org) contains Fig. 1S and Table IIS.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBank™/EMBL Data Bank with accession number(s) (for NCBE).

Supported by a Japan Society for the Promotion of Science (JSPS) postdoctoral fellowship for foreign researchers.

Supported by a JSPS research fellowship for young scientists.