Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools

Autores
De Giusti, Verónica Celeste; Orlowski, Alejandro; Villa Abrille, María Celeste; Chiappe de Cingolani, Gladys Ethel; Casey, Joseph R.; Álvarez, Bernardo Víctor; Aiello, Ernesto Alejandro
Año de publicación
2011
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Background and purpose: Na⁺/HCO3⁻ co-transport (NBC) regulates intracellular pH (pHi) in the heart. We have studied the electrogenic NBC isoform NBCe1 by examining the effect of functional antibodies to this protein. Experimental approach: We generated two antibodies against putative extracellular loop domains 3 (a-L3) and 4 (a-L4) of NBCe1 which recognized NBCe1 on immunoblots and immunostaining experiments. pHi was monitored using epi-fluorescence measurements in cat ventricular myocytes. Transport activity of total NBC and of NBCe1 in isolation were evaluated after an ammonium ion-induced acidosis (expressed as H⁺ flux, JH, in mmol·L-1 min-1 at pHi 6.8) and during membrane depolarization with high extracellular potassium (potassium pulse, expressed as ΔpHi) respectively. Key results: The potassium pulse produced a pHi increase of 0.18 ± 0.006 (n= 5), which was reduced by the a-L3 antibody (0.016 ± 0.019). The a-L-3 also decreased JH by 50%. Surprisingly, during the potassium pulse, a-L4 induced a higher pHi increase than control,(0.25 ± 0.018) whereas the recovery of pHi from acidosis was faster (JH was almost double the control value). In perforated-patch experiments, a-L3 prolonged and a-L4 shortened action potential duration, consistent with blockade and stimulation of NBCe1-carried anionic current respectively. Conclusions and implications: Both antibodies recognized NBCe1, but they had opposing effects on the function of this transporter, as the a-L3 was inhibitory and the a-L4 was excitatory. These antibodies could be valuable in studies on the pathophysiology of NBCe1 in cardiac tissue, opening a path for their potential clinical use.
Facultad de Ciencias Médicas
Centro de Investigaciones Cardiovasculares
Materia
Medicina
Cardiac myocytes
Functional antibodies
Na⁺/HCO3⁻ co-transporter
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/97962

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network_name_str SEDICI (UNLP)
spelling Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological toolsDe Giusti, Verónica CelesteOrlowski, AlejandroVilla Abrille, María CelesteChiappe de Cingolani, Gladys EthelCasey, Joseph R.Álvarez, Bernardo VíctorAiello, Ernesto AlejandroMedicinaCardiac myocytesFunctional antibodiesNa⁺/HCO3⁻ co-transporterBackground and purpose: Na⁺/HCO<sub>3</sub>⁻ co-transport (NBC) regulates intracellular pH (pH<sub>i</sub>) in the heart. We have studied the electrogenic NBC isoform NBCe1 by examining the effect of functional antibodies to this protein. Experimental approach: We generated two antibodies against putative extracellular loop domains 3 (a-L3) and 4 (a-L4) of NBCe1 which recognized NBCe1 on immunoblots and immunostaining experiments. pH<sub>i</sub> was monitored using epi-fluorescence measurements in cat ventricular myocytes. Transport activity of total NBC and of NBCe1 in isolation were evaluated after an ammonium ion-induced acidosis (expressed as H⁺ flux, J<sub>H</sub>, in mmol·L<sup>-1</sup> min<sup>-1</sup> at pH<sub>i</sub> 6.8) and during membrane depolarization with high extracellular potassium (potassium pulse, expressed as ΔpH<sub>i</sub>) respectively. Key results: The potassium pulse produced a pH<sub>i</sub> increase of 0.18 ± 0.006 (n= 5), which was reduced by the a-L3 antibody (0.016 ± 0.019). The a-L-3 also decreased J<sub>H</sub> by 50%. Surprisingly, during the potassium pulse, a-L4 induced a higher pH<sub>i</sub> increase than control,(0.25 ± 0.018) whereas the recovery of pH<sub>i</sub> from acidosis was faster (J<sub>H</sub> was almost double the control value). In perforated-patch experiments, a-L3 prolonged and a-L4 shortened action potential duration, consistent with blockade and stimulation of NBCe1-carried anionic current respectively. Conclusions and implications: Both antibodies recognized NBCe1, but they had opposing effects on the function of this transporter, as the a-L3 was inhibitory and the a-L4 was excitatory. These antibodies could be valuable in studies on the pathophysiology of NBCe1 in cardiac tissue, opening a path for their potential clinical use.Facultad de Ciencias MédicasCentro de Investigaciones Cardiovasculares2011-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1976-1989http://sedici.unlp.edu.ar/handle/10915/97962enginfo:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/61760info:eu-repo/semantics/altIdentifier/url/https://bpspubs.onlinelibrary.wiley.com/doi/abs/10.1111/j.1476-5381.2011.01496.xinfo:eu-repo/semantics/altIdentifier/issn/0007-1188info:eu-repo/semantics/altIdentifier/doi/10.1111/j.1476-5381.2011.01496.xinfo:eu-repo/semantics/altIdentifier/hdl/11336/61760info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T10:52:31Zoai:sedici.unlp.edu.ar:10915/97962Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 10:52:31.548SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
title Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
spellingShingle Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
De Giusti, Verónica Celeste
Medicina
Cardiac myocytes
Functional antibodies
Na⁺/HCO3⁻ co-transporter
title_short Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
title_full Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
title_fullStr Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
title_full_unstemmed Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
title_sort Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
dc.creator.none.fl_str_mv De Giusti, Verónica Celeste
Orlowski, Alejandro
Villa Abrille, María Celeste
Chiappe de Cingolani, Gladys Ethel
Casey, Joseph R.
Álvarez, Bernardo Víctor
Aiello, Ernesto Alejandro
author De Giusti, Verónica Celeste
author_facet De Giusti, Verónica Celeste
Orlowski, Alejandro
Villa Abrille, María Celeste
Chiappe de Cingolani, Gladys Ethel
Casey, Joseph R.
Álvarez, Bernardo Víctor
Aiello, Ernesto Alejandro
author_role author
author2 Orlowski, Alejandro
Villa Abrille, María Celeste
Chiappe de Cingolani, Gladys Ethel
Casey, Joseph R.
Álvarez, Bernardo Víctor
Aiello, Ernesto Alejandro
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv Medicina
Cardiac myocytes
Functional antibodies
Na⁺/HCO3⁻ co-transporter
topic Medicina
Cardiac myocytes
Functional antibodies
Na⁺/HCO3⁻ co-transporter
dc.description.none.fl_txt_mv Background and purpose: Na⁺/HCO<sub>3</sub>⁻ co-transport (NBC) regulates intracellular pH (pH<sub>i</sub>) in the heart. We have studied the electrogenic NBC isoform NBCe1 by examining the effect of functional antibodies to this protein. Experimental approach: We generated two antibodies against putative extracellular loop domains 3 (a-L3) and 4 (a-L4) of NBCe1 which recognized NBCe1 on immunoblots and immunostaining experiments. pH<sub>i</sub> was monitored using epi-fluorescence measurements in cat ventricular myocytes. Transport activity of total NBC and of NBCe1 in isolation were evaluated after an ammonium ion-induced acidosis (expressed as H⁺ flux, J<sub>H</sub>, in mmol·L<sup>-1</sup> min<sup>-1</sup> at pH<sub>i</sub> 6.8) and during membrane depolarization with high extracellular potassium (potassium pulse, expressed as ΔpH<sub>i</sub>) respectively. Key results: The potassium pulse produced a pH<sub>i</sub> increase of 0.18 ± 0.006 (n= 5), which was reduced by the a-L3 antibody (0.016 ± 0.019). The a-L-3 also decreased J<sub>H</sub> by 50%. Surprisingly, during the potassium pulse, a-L4 induced a higher pH<sub>i</sub> increase than control,(0.25 ± 0.018) whereas the recovery of pH<sub>i</sub> from acidosis was faster (J<sub>H</sub> was almost double the control value). In perforated-patch experiments, a-L3 prolonged and a-L4 shortened action potential duration, consistent with blockade and stimulation of NBCe1-carried anionic current respectively. Conclusions and implications: Both antibodies recognized NBCe1, but they had opposing effects on the function of this transporter, as the a-L3 was inhibitory and the a-L4 was excitatory. These antibodies could be valuable in studies on the pathophysiology of NBCe1 in cardiac tissue, opening a path for their potential clinical use.
Facultad de Ciencias Médicas
Centro de Investigaciones Cardiovasculares
description Background and purpose: Na⁺/HCO<sub>3</sub>⁻ co-transport (NBC) regulates intracellular pH (pH<sub>i</sub>) in the heart. We have studied the electrogenic NBC isoform NBCe1 by examining the effect of functional antibodies to this protein. Experimental approach: We generated two antibodies against putative extracellular loop domains 3 (a-L3) and 4 (a-L4) of NBCe1 which recognized NBCe1 on immunoblots and immunostaining experiments. pH<sub>i</sub> was monitored using epi-fluorescence measurements in cat ventricular myocytes. Transport activity of total NBC and of NBCe1 in isolation were evaluated after an ammonium ion-induced acidosis (expressed as H⁺ flux, J<sub>H</sub>, in mmol·L<sup>-1</sup> min<sup>-1</sup> at pH<sub>i</sub> 6.8) and during membrane depolarization with high extracellular potassium (potassium pulse, expressed as ΔpH<sub>i</sub>) respectively. Key results: The potassium pulse produced a pH<sub>i</sub> increase of 0.18 ± 0.006 (n= 5), which was reduced by the a-L3 antibody (0.016 ± 0.019). The a-L-3 also decreased J<sub>H</sub> by 50%. Surprisingly, during the potassium pulse, a-L4 induced a higher pH<sub>i</sub> increase than control,(0.25 ± 0.018) whereas the recovery of pH<sub>i</sub> from acidosis was faster (J<sub>H</sub> was almost double the control value). In perforated-patch experiments, a-L3 prolonged and a-L4 shortened action potential duration, consistent with blockade and stimulation of NBCe1-carried anionic current respectively. Conclusions and implications: Both antibodies recognized NBCe1, but they had opposing effects on the function of this transporter, as the a-L3 was inhibitory and the a-L4 was excitatory. These antibodies could be valuable in studies on the pathophysiology of NBCe1 in cardiac tissue, opening a path for their potential clinical use.
publishDate 2011
dc.date.none.fl_str_mv 2011-12
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info:eu-repo/semantics/publishedVersion
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url http://sedici.unlp.edu.ar/handle/10915/97962
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/61760
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info:eu-repo/semantics/altIdentifier/issn/0007-1188
info:eu-repo/semantics/altIdentifier/doi/10.1111/j.1476-5381.2011.01496.x
info:eu-repo/semantics/altIdentifier/hdl/11336/61760
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
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