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Binding of carbonic anhydrase IX to extracellular loop 4 of the NBCe1 Na + /HCO 3 − cotransporter enhances NBCe1-mediated HCO 3 − influx in the rat heart

Orlowski, Alejandro et al · American Physiological Society · 2012

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Na(+)/HCO(3)(-) cotransporter (NBC)e1 catalyze the electrogenic movement of 1 Na(+):2 HCO(3)(-) into cardiomyocytes cytosol. NBC proteins associate with carbonic anhydrases (CA), CAII, and CAIV, forming a HCO(3)(-) transport metabolon. Herein, we examined the physical/functional interaction of NBCe1 and transmembrane CAIX in cardiac muscle. NBCe1 and CAIX physical association was examined by coimmunoprecipitation, using rat ventricular lysates. NBCe1 coimmunoprecipitated with anti-CAIX antibody, indicating NBCe1 and CAIX interaction in the myocardium. Glutathione-S-transferase (GST) pull-down assays with predicted extracellular loops (EC) of NBCe1 revealed that NBCe1-EC4 mediated interaction with CAIX. Functional NBCe1/CAIX interaction was examined using fluorescence measurements of BCECF in rat cardiomyocytes to monitor cytosolic pH. NBCe1 transport activity was evaluated after membrane depolarization with high extracellular K(+) in the presence or absence of the CA inhibitors, benzolamide (BZ; 100 μM) or 6-ethoxyzolamide (ETZ; 100 μM) (*P < 0.05). This depolarization protocol produced an intracellular pH (pH(i)) increase of 0.17 ± 0.01 (n = 11), which was inhibited by BZ (0.11 ± 0.02; n = 7) or ETZ (0.06 ± 0.01; n = 6). NBCe1 activity was also measured by changes of pH(i) in NBCe1-transfected human embryonic kidney 293 cells subjected to acid loads. Cotransfection of CAIX with NBCe1 increased the rate of pH(i) recovery (in mM/min) by about fourfold (12.1 ± 0.8; n = 9) compared with cells expressing NBCe1 alone (3.1 ± 0.5; n = 7), which was inhibited by BZ (7.5 ± 0.3; n = 9). We demonstrated that CAIX forms a complex with EC4 of NBCe1, which activates NBCe1-mediated HCO(3)(-) influx in the myocardium. CAIX and NBCe1 have been linked to tumorigenesis and cardiac cell growth, respectively. Thus inhibition of CA activity might be useful to prevent activation of NBCe1 under these pathological conditions. Fil: Orlowski, Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigaciones Cardiovasculares "Dr. Horacio Eugenio Cingolani". Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Centro de Investigaciones Cardiovasculares "Dr. Horacio Eugenio Cingolani"; Argentina Fil: de Giusti, Verónica Celeste. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigaciones Cardiovasculares "Dr. Horacio Eugenio Cingolani". Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Centro de Investigaciones Cardiovasculares "Dr. Horacio Eugenio Cingolani"; Argentina

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APA 7

Orlowski, A. E. A. (2012). Binding of carbonic anhydrase IX to extracellular loop 4 of the NBCe1 Na + /HCO 3 − cotransporter enhances NBCe1-mediated HCO 3 − influx in the rat heart. http://hdl.handle.net/11336/270483

MLA

Orlowski, Alejandro et al. "Binding of carbonic anhydrase IX to extracellular loop 4 of the NBCe1 Na + /HCO 3 − cotransporter enhances NBCe1-mediated HCO 3 − influx in the rat heart." 2012. http://hdl.handle.net/11336/270483.

Chicago

Orlowski, Alejandro et al. 2012. "Binding of carbonic anhydrase IX to extracellular loop 4 of the NBCe1 Na + /HCO 3 − cotransporter enhances NBCe1-mediated HCO 3 − influx in the rat heart.". http://hdl.handle.net/11336/270483.

Harvard

Orlowski, A. E. A. 2012, Binding of carbonic anhydrase IX to extracellular loop 4 of the NBCe1 Na + /HCO 3 − cotransporter enhances NBCe1-mediated HCO 3 − influx in the rat heart, American Physiological Society, available at: http://hdl.handle.net/11336/270483 [Accessed 29 Jun. 2026].

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Título
Binding of carbonic anhydrase IX to extracellular loop 4 of the NBCe1 Na + /HCO 3 − cotransporter enhances NBCe1-mediated HCO 3 − influx in the rat heart
Autor / colaboradores
Orlowski, Alejandro et al
Editorial
American Physiological Society
Año de publicación
2012
ISSN
0363-6143
ISSN
0363-6143
Idioma
eng

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