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
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/97962
Ver los metadatos del registro completo
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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 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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http://sedici.unlp.edu.ar/handle/10915/97962 |
url |
http://sedici.unlp.edu.ar/handle/10915/97962 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
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info:eu-repo/semantics/openAccess 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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openAccess |
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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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