Bicarbonate homeostasis in excitable tissues: role of AE3 Cl⁻/HCO⁻₃ exchanger and carbonic anhydrase XIV interaction

Bicarbonate transport and metabolism are key elements of normal cellular function. Two alternate transcripts of anion exchanger 3 (AE3), full-length (AE3fl) and cardiac (AE3c), are expressed in central nervous system (CNS), where AE3 catalyzes electroneutral Cl⁻/HCO3− exchange across the plasma memb...

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Autores principales: Casey, Joseph R., Sly, William S., Shah, Gul N., Álvarez, Bernardo Víctor
Formato: Articulo
Lenguaje:Inglés
Publicado: 2009
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Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/123697
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id I19-R120-10915-123697
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Bioquímica
Bicarbonate transport metabolon
AE3/CAXIV complex
Central nervous system
spellingShingle Bioquímica
Bicarbonate transport metabolon
AE3/CAXIV complex
Central nervous system
Casey, Joseph R.
Sly, William S.
Shah, Gul N.
Álvarez, Bernardo Víctor
Bicarbonate homeostasis in excitable tissues: role of AE3 Cl⁻/HCO⁻₃ exchanger and carbonic anhydrase XIV interaction
topic_facet Bioquímica
Bicarbonate transport metabolon
AE3/CAXIV complex
Central nervous system
description Bicarbonate transport and metabolism are key elements of normal cellular function. Two alternate transcripts of anion exchanger 3 (AE3), full-length (AE3fl) and cardiac (AE3c), are expressed in central nervous system (CNS), where AE3 catalyzes electroneutral Cl⁻/HCO3− exchange across the plasma membrane of neuronal and glial cells of CNS. Anion exchanger isoforms, AE3fl and AE3c, associate with the carbonic anhydrases (CA) CAII and CAIV, forming a HCO3− transport metabolon, to maximize HCO3− flux across the plasma membrane. CAXIV, with catalytic domain anchored to the extracellular surface, is also expressed in CNS. Here physical association of AE3 and CAXIV was examined by coimmunoprecipitation experiments, using mouse brain and retinal lysates. CAXIV immunoprecipitated with anti-AE3 antibody, and both AE3 isoforms were immunoprecipitated using anti-CAXIV antibody, indicating CAXIV and AE3 interaction in the CNS. Confocal images revealed colocalization of CAXIV and AE3 in Muller and horizontal cells, in the mouse retina. Cl⁻/HCO3− exchange activity of AE3fl was investigated in transiently transfected human embryonic kidney 293 cells, using intracellular fluorescence measurements of BCECF, to monitor intracellular pH. CAXIV increased the rate of AE3fl-mediated HCO3− transport by up to 120%, which was suppressed by the CA inhibitor acetazolamide. Association of AE3 and CAXIV may represent a mechanism to enhance disposal of waste CO₂ and to balance pH in excitable tissues.
format Articulo
Articulo
author Casey, Joseph R.
Sly, William S.
Shah, Gul N.
Álvarez, Bernardo Víctor
author_facet Casey, Joseph R.
Sly, William S.
Shah, Gul N.
Álvarez, Bernardo Víctor
author_sort Casey, Joseph R.
title Bicarbonate homeostasis in excitable tissues: role of AE3 Cl⁻/HCO⁻₃ exchanger and carbonic anhydrase XIV interaction
title_short Bicarbonate homeostasis in excitable tissues: role of AE3 Cl⁻/HCO⁻₃ exchanger and carbonic anhydrase XIV interaction
title_full Bicarbonate homeostasis in excitable tissues: role of AE3 Cl⁻/HCO⁻₃ exchanger and carbonic anhydrase XIV interaction
title_fullStr Bicarbonate homeostasis in excitable tissues: role of AE3 Cl⁻/HCO⁻₃ exchanger and carbonic anhydrase XIV interaction
title_full_unstemmed Bicarbonate homeostasis in excitable tissues: role of AE3 Cl⁻/HCO⁻₃ exchanger and carbonic anhydrase XIV interaction
title_sort bicarbonate homeostasis in excitable tissues: role of ae3 cl⁻/hco⁻₃ exchanger and carbonic anhydrase xiv interaction
publishDate 2009
url http://sedici.unlp.edu.ar/handle/10915/123697
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