Modulation of extracellular ph in cystic fibrosis cells by egfr
- Autores
- Massip Copiz, María Macarena; Valdivieso, Ángel Gabriel; Asensio, Cristian Jorge Alejandro; Santa Coloma, Tomás Antonio
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- Cystic fibrosis (CF) is an inherited disease caused by mutations inthe CFTR (CF transmembrane conductance regulator) gene. It isprincipally characterized by chronic infections and persistent inflammation in lungs. One of the hypotheses that tried to explain the increased susceptibility to lung infections is the reduction in the airwaysurface liquid (ASL) pH. The changes observed in the extracellularpH (pHe) could be a consequence of a reduced bicarbonate transport through CFTR and also an increase in lactic acid secretion.Considering that the EGFR pathway is affected in the CF phenotype, the aim of the present work was to determine if the EGFRpathway is involved in the extracellular pH regulation in CF cells.Two cellular models were used: IB3-1 cells (CF cells) and C38 cells(IB3-1 ?corrected? cells). Together with the extracellular pH and lacticacid (lactate) secretion measurements, LDH expression and activitywere performed by RT-PCR, Western Blot, flow cytometry, confocalmicroscopy and spectrophotometric techniques. The results reported a decrease in pH in the extracellular medium culture (p<0.05) inIB3-1 cells concomitantly with an increased in lactate secretion andboth LDH expression and activity (p<0.05) compared with C38 cells.Studying the role of EGFR in pH regulation, we observed that inhibition of EGFR restores the pH in the extracellular medium (p<0.05),the lactate secretion (p<0.05) and the LDH expression and activity (p<0.05) in CF cells. In conclusion, our results confirmed that aconstitutive EGFR activation is partially involved in the regulationof pHe, lactic acid secretion and LDH expression and activity bythe CFTR channel. The low pH microenvironment observed in CFcells could interfere with immunological functions and promote theestablishment of infections in patients with CF.
Fil: Massip Copiz, María Macarena. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; Argentina
Fil: Valdivieso, Ángel Gabriel. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; Argentina
Fil: Asensio, Cristian Jorge Alejandro. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; Argentina
Fil: Santa Coloma, Tomás Antonio. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; Argentina
LXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión anual de la Sociedad Argentina de Immunología; LIII Reunión anual de la Asociación Argentina de Farmacología Experimental y XI Reunión anual de la Asociación Argentina de Nanomedicinas
Argentina
Sociedad Argentina de Inmunología
Asociación Argentina de Farmacología Experimental
Sociedad Argentina de Investigación Clínica
Asociación Argentina de Nanomedicinas - Materia
-
PH
CYSTIC FIBROSIS
CFTR
EGFR - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/280749
Ver los metadatos del registro completo
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Modulation of extracellular ph in cystic fibrosis cells by egfrMassip Copiz, María MacarenaValdivieso, Ángel GabrielAsensio, Cristian Jorge AlejandroSanta Coloma, Tomás AntonioPHCYSTIC FIBROSISCFTREGFRhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Cystic fibrosis (CF) is an inherited disease caused by mutations inthe CFTR (CF transmembrane conductance regulator) gene. It isprincipally characterized by chronic infections and persistent inflammation in lungs. One of the hypotheses that tried to explain the increased susceptibility to lung infections is the reduction in the airwaysurface liquid (ASL) pH. The changes observed in the extracellularpH (pHe) could be a consequence of a reduced bicarbonate transport through CFTR and also an increase in lactic acid secretion.Considering that the EGFR pathway is affected in the CF phenotype, the aim of the present work was to determine if the EGFRpathway is involved in the extracellular pH regulation in CF cells.Two cellular models were used: IB3-1 cells (CF cells) and C38 cells(IB3-1 ?corrected? cells). Together with the extracellular pH and lacticacid (lactate) secretion measurements, LDH expression and activitywere performed by RT-PCR, Western Blot, flow cytometry, confocalmicroscopy and spectrophotometric techniques. The results reported a decrease in pH in the extracellular medium culture (p<0.05) inIB3-1 cells concomitantly with an increased in lactate secretion andboth LDH expression and activity (p<0.05) compared with C38 cells.Studying the role of EGFR in pH regulation, we observed that inhibition of EGFR restores the pH in the extracellular medium (p<0.05),the lactate secretion (p<0.05) and the LDH expression and activity (p<0.05) in CF cells. In conclusion, our results confirmed that aconstitutive EGFR activation is partially involved in the regulationof pHe, lactic acid secretion and LDH expression and activity bythe CFTR channel. The low pH microenvironment observed in CFcells could interfere with immunological functions and promote theestablishment of infections in patients with CF.Fil: Massip Copiz, María Macarena. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; ArgentinaFil: Valdivieso, Ángel Gabriel. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; ArgentinaFil: Asensio, Cristian Jorge Alejandro. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; ArgentinaFil: Santa Coloma, Tomás Antonio. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; ArgentinaLXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión anual de la Sociedad Argentina de Immunología; LIII Reunión anual de la Asociación Argentina de Farmacología Experimental y XI Reunión anual de la Asociación Argentina de NanomedicinasArgentinaSociedad Argentina de InmunologíaAsociación Argentina de Farmacología ExperimentalSociedad Argentina de Investigación ClínicaAsociación Argentina de NanomedicinasFundación Revista Medicina2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/280749Modulation of extracellular ph in cystic fibrosis cells by egfr; LXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión anual de la Sociedad Argentina de Immunología; LIII Reunión anual de la Asociación Argentina de Farmacología Experimental y XI Reunión anual de la Asociación Argentina de Nanomedicinas; Argentina; 2021; 250-2501669-9106CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.reunionbiociencias.com.ar/wp-content/uploads/2021/11/Revista-Medicina-2021.pdfNacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-02-26T10:28:42Zoai:ri.conicet.gov.ar:11336/280749instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982026-02-26 10:28:43.259CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Modulation of extracellular ph in cystic fibrosis cells by egfr |
| title |
Modulation of extracellular ph in cystic fibrosis cells by egfr |
| spellingShingle |
Modulation of extracellular ph in cystic fibrosis cells by egfr Massip Copiz, María Macarena PH CYSTIC FIBROSIS CFTR EGFR |
| title_short |
Modulation of extracellular ph in cystic fibrosis cells by egfr |
| title_full |
Modulation of extracellular ph in cystic fibrosis cells by egfr |
| title_fullStr |
Modulation of extracellular ph in cystic fibrosis cells by egfr |
| title_full_unstemmed |
Modulation of extracellular ph in cystic fibrosis cells by egfr |
| title_sort |
Modulation of extracellular ph in cystic fibrosis cells by egfr |
| dc.creator.none.fl_str_mv |
Massip Copiz, María Macarena Valdivieso, Ángel Gabriel Asensio, Cristian Jorge Alejandro Santa Coloma, Tomás Antonio |
| author |
Massip Copiz, María Macarena |
| author_facet |
Massip Copiz, María Macarena Valdivieso, Ángel Gabriel Asensio, Cristian Jorge Alejandro Santa Coloma, Tomás Antonio |
| author_role |
author |
| author2 |
Valdivieso, Ángel Gabriel Asensio, Cristian Jorge Alejandro Santa Coloma, Tomás Antonio |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
PH CYSTIC FIBROSIS CFTR EGFR |
| topic |
PH CYSTIC FIBROSIS CFTR EGFR |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
Cystic fibrosis (CF) is an inherited disease caused by mutations inthe CFTR (CF transmembrane conductance regulator) gene. It isprincipally characterized by chronic infections and persistent inflammation in lungs. One of the hypotheses that tried to explain the increased susceptibility to lung infections is the reduction in the airwaysurface liquid (ASL) pH. The changes observed in the extracellularpH (pHe) could be a consequence of a reduced bicarbonate transport through CFTR and also an increase in lactic acid secretion.Considering that the EGFR pathway is affected in the CF phenotype, the aim of the present work was to determine if the EGFRpathway is involved in the extracellular pH regulation in CF cells.Two cellular models were used: IB3-1 cells (CF cells) and C38 cells(IB3-1 ?corrected? cells). Together with the extracellular pH and lacticacid (lactate) secretion measurements, LDH expression and activitywere performed by RT-PCR, Western Blot, flow cytometry, confocalmicroscopy and spectrophotometric techniques. The results reported a decrease in pH in the extracellular medium culture (p<0.05) inIB3-1 cells concomitantly with an increased in lactate secretion andboth LDH expression and activity (p<0.05) compared with C38 cells.Studying the role of EGFR in pH regulation, we observed that inhibition of EGFR restores the pH in the extracellular medium (p<0.05),the lactate secretion (p<0.05) and the LDH expression and activity (p<0.05) in CF cells. In conclusion, our results confirmed that aconstitutive EGFR activation is partially involved in the regulationof pHe, lactic acid secretion and LDH expression and activity bythe CFTR channel. The low pH microenvironment observed in CFcells could interfere with immunological functions and promote theestablishment of infections in patients with CF. Fil: Massip Copiz, María Macarena. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; Argentina Fil: Valdivieso, Ángel Gabriel. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; Argentina Fil: Asensio, Cristian Jorge Alejandro. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; Argentina Fil: Santa Coloma, Tomás Antonio. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; Argentina LXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; LXIX Reunión anual de la Sociedad Argentina de Immunología; LIII Reunión anual de la Asociación Argentina de Farmacología Experimental y XI Reunión anual de la Asociación Argentina de Nanomedicinas Argentina Sociedad Argentina de Inmunología Asociación Argentina de Farmacología Experimental Sociedad Argentina de Investigación Clínica Asociación Argentina de Nanomedicinas |
| description |
Cystic fibrosis (CF) is an inherited disease caused by mutations inthe CFTR (CF transmembrane conductance regulator) gene. It isprincipally characterized by chronic infections and persistent inflammation in lungs. One of the hypotheses that tried to explain the increased susceptibility to lung infections is the reduction in the airwaysurface liquid (ASL) pH. The changes observed in the extracellularpH (pHe) could be a consequence of a reduced bicarbonate transport through CFTR and also an increase in lactic acid secretion.Considering that the EGFR pathway is affected in the CF phenotype, the aim of the present work was to determine if the EGFRpathway is involved in the extracellular pH regulation in CF cells.Two cellular models were used: IB3-1 cells (CF cells) and C38 cells(IB3-1 ?corrected? cells). Together with the extracellular pH and lacticacid (lactate) secretion measurements, LDH expression and activitywere performed by RT-PCR, Western Blot, flow cytometry, confocalmicroscopy and spectrophotometric techniques. The results reported a decrease in pH in the extracellular medium culture (p<0.05) inIB3-1 cells concomitantly with an increased in lactate secretion andboth LDH expression and activity (p<0.05) compared with C38 cells.Studying the role of EGFR in pH regulation, we observed that inhibition of EGFR restores the pH in the extracellular medium (p<0.05),the lactate secretion (p<0.05) and the LDH expression and activity (p<0.05) in CF cells. In conclusion, our results confirmed that aconstitutive EGFR activation is partially involved in the regulationof pHe, lactic acid secretion and LDH expression and activity bythe CFTR channel. The low pH microenvironment observed in CFcells could interfere with immunological functions and promote theestablishment of infections in patients with CF. |
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2021 |
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2021 |
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