Molecular mechanisms of cell death in a mouse model of progressive hearing loss
- Autores
- Carignano, Camila; Vera, Marcela Sonia; Dionisio, Leonardo Raul; Aztiria, Eugenio Manuel; Rias, Ezequiel Ignacio; Spitzmaul, Guillermo Federico
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- KCNQ4 is a voltage-gated K+ channel whose dysfunction in the inner ear is the main cause of the progressive hearing loss (HL) DFNA2. It develops in 2 phases: first, a mild HL (40-60 dB) and later, it progresses to a profound HL (> 90 dB). Previously, using a knock out mouse model of the human DFNA2 (Kcnq4-/-), we reported that outer hair cell (OHC) degeneration may explain the first phase of HL and inner hair cell (IHC) and spiral ganglion neuron (SGN) degeneration occur in the second phase of HL. Now, we performed a functional hearing test, correlating these results with the molecular events leading to cell death and ultrastructural changes in the Organ of Corti’s surface in both phases. We observed a profound HL starting at middle-aged (40-week-old (W)) Kcnq4-/- mice, as revealed by Preyer´s reflex test. By immunofluorescence, we found caspase 3- mediated apoptosis (Cas-3) in SGNs and OHCs of Kcnq4-/- mice at different time points: in SGNs it was found late, at 54W and 68W, which correlates with our functional studies elucidating the profound HL of the last phase. On the other hand, OHCs showed a Cas-3 positive signal in 4W and 10W Kcnq4-/- mice, which could explain the mild HL of the first phase of DFNA2. IHCs did not show Cas-3 signal but they exhibited remarkable stereocilia defects by scanning microscopy, such as fusion and giant stereocilia in old mice. Collectively, these results are useful to understand the mechanisms involved in the human DFNA2.
Fil: Carignano, Camila. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Vera, Marcela Sonia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Dionisio, Leonardo Raul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Aztiria, Eugenio Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Rias, Ezequiel Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Spitzmaul, Guillermo Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
XXXV Annual Meeting of the Argentinian Society for Neuroscience Research
Buenos Aires
Argentina
Sociedad Argentina de Investigación en Neurociencias - Materia
-
HEARING LOSS
KCNQ4
DFNA2
APOPTOSIS - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/155864
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Molecular mechanisms of cell death in a mouse model of progressive hearing lossCarignano, CamilaVera, Marcela SoniaDionisio, Leonardo RaulAztiria, Eugenio ManuelRias, Ezequiel IgnacioSpitzmaul, Guillermo FedericoHEARING LOSSKCNQ4DFNA2APOPTOSIShttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3KCNQ4 is a voltage-gated K+ channel whose dysfunction in the inner ear is the main cause of the progressive hearing loss (HL) DFNA2. It develops in 2 phases: first, a mild HL (40-60 dB) and later, it progresses to a profound HL (> 90 dB). Previously, using a knock out mouse model of the human DFNA2 (Kcnq4-/-), we reported that outer hair cell (OHC) degeneration may explain the first phase of HL and inner hair cell (IHC) and spiral ganglion neuron (SGN) degeneration occur in the second phase of HL. Now, we performed a functional hearing test, correlating these results with the molecular events leading to cell death and ultrastructural changes in the Organ of Corti’s surface in both phases. We observed a profound HL starting at middle-aged (40-week-old (W)) Kcnq4-/- mice, as revealed by Preyer´s reflex test. By immunofluorescence, we found caspase 3- mediated apoptosis (Cas-3) in SGNs and OHCs of Kcnq4-/- mice at different time points: in SGNs it was found late, at 54W and 68W, which correlates with our functional studies elucidating the profound HL of the last phase. On the other hand, OHCs showed a Cas-3 positive signal in 4W and 10W Kcnq4-/- mice, which could explain the mild HL of the first phase of DFNA2. IHCs did not show Cas-3 signal but they exhibited remarkable stereocilia defects by scanning microscopy, such as fusion and giant stereocilia in old mice. Collectively, these results are useful to understand the mechanisms involved in the human DFNA2.Fil: Carignano, Camila. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Vera, Marcela Sonia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Dionisio, Leonardo Raul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Aztiria, Eugenio Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Rias, Ezequiel Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Spitzmaul, Guillermo Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaXXXV Annual Meeting of the Argentinian Society for Neuroscience ResearchBuenos AiresArgentinaSociedad Argentina de Investigación en NeurocienciasSociedad Argentina de Investigación en Neurociencias2020info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/155864Molecular mechanisms of cell death in a mouse model of progressive hearing loss; XXXV Annual Meeting of the Argentinian Society for Neuroscience Research; Buenos Aires; Argentina; 2020; 320-320CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://san2020.saneurociencias.org.ar/Nacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:53:31Zoai:ri.conicet.gov.ar:11336/155864instacron: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:34982025-09-03 09:53:31.823CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Molecular mechanisms of cell death in a mouse model of progressive hearing loss |
title |
Molecular mechanisms of cell death in a mouse model of progressive hearing loss |
spellingShingle |
Molecular mechanisms of cell death in a mouse model of progressive hearing loss Carignano, Camila HEARING LOSS KCNQ4 DFNA2 APOPTOSIS |
title_short |
Molecular mechanisms of cell death in a mouse model of progressive hearing loss |
title_full |
Molecular mechanisms of cell death in a mouse model of progressive hearing loss |
title_fullStr |
Molecular mechanisms of cell death in a mouse model of progressive hearing loss |
title_full_unstemmed |
Molecular mechanisms of cell death in a mouse model of progressive hearing loss |
title_sort |
Molecular mechanisms of cell death in a mouse model of progressive hearing loss |
dc.creator.none.fl_str_mv |
Carignano, Camila Vera, Marcela Sonia Dionisio, Leonardo Raul Aztiria, Eugenio Manuel Rias, Ezequiel Ignacio Spitzmaul, Guillermo Federico |
author |
Carignano, Camila |
author_facet |
Carignano, Camila Vera, Marcela Sonia Dionisio, Leonardo Raul Aztiria, Eugenio Manuel Rias, Ezequiel Ignacio Spitzmaul, Guillermo Federico |
author_role |
author |
author2 |
Vera, Marcela Sonia Dionisio, Leonardo Raul Aztiria, Eugenio Manuel Rias, Ezequiel Ignacio Spitzmaul, Guillermo Federico |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
HEARING LOSS KCNQ4 DFNA2 APOPTOSIS |
topic |
HEARING LOSS KCNQ4 DFNA2 APOPTOSIS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
KCNQ4 is a voltage-gated K+ channel whose dysfunction in the inner ear is the main cause of the progressive hearing loss (HL) DFNA2. It develops in 2 phases: first, a mild HL (40-60 dB) and later, it progresses to a profound HL (> 90 dB). Previously, using a knock out mouse model of the human DFNA2 (Kcnq4-/-), we reported that outer hair cell (OHC) degeneration may explain the first phase of HL and inner hair cell (IHC) and spiral ganglion neuron (SGN) degeneration occur in the second phase of HL. Now, we performed a functional hearing test, correlating these results with the molecular events leading to cell death and ultrastructural changes in the Organ of Corti’s surface in both phases. We observed a profound HL starting at middle-aged (40-week-old (W)) Kcnq4-/- mice, as revealed by Preyer´s reflex test. By immunofluorescence, we found caspase 3- mediated apoptosis (Cas-3) in SGNs and OHCs of Kcnq4-/- mice at different time points: in SGNs it was found late, at 54W and 68W, which correlates with our functional studies elucidating the profound HL of the last phase. On the other hand, OHCs showed a Cas-3 positive signal in 4W and 10W Kcnq4-/- mice, which could explain the mild HL of the first phase of DFNA2. IHCs did not show Cas-3 signal but they exhibited remarkable stereocilia defects by scanning microscopy, such as fusion and giant stereocilia in old mice. Collectively, these results are useful to understand the mechanisms involved in the human DFNA2. Fil: Carignano, Camila. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Vera, Marcela Sonia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Dionisio, Leonardo Raul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Aztiria, Eugenio Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Rias, Ezequiel Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Spitzmaul, Guillermo Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina XXXV Annual Meeting of the Argentinian Society for Neuroscience Research Buenos Aires Argentina Sociedad Argentina de Investigación en Neurociencias |
description |
KCNQ4 is a voltage-gated K+ channel whose dysfunction in the inner ear is the main cause of the progressive hearing loss (HL) DFNA2. It develops in 2 phases: first, a mild HL (40-60 dB) and later, it progresses to a profound HL (> 90 dB). Previously, using a knock out mouse model of the human DFNA2 (Kcnq4-/-), we reported that outer hair cell (OHC) degeneration may explain the first phase of HL and inner hair cell (IHC) and spiral ganglion neuron (SGN) degeneration occur in the second phase of HL. Now, we performed a functional hearing test, correlating these results with the molecular events leading to cell death and ultrastructural changes in the Organ of Corti’s surface in both phases. We observed a profound HL starting at middle-aged (40-week-old (W)) Kcnq4-/- mice, as revealed by Preyer´s reflex test. By immunofluorescence, we found caspase 3- mediated apoptosis (Cas-3) in SGNs and OHCs of Kcnq4-/- mice at different time points: in SGNs it was found late, at 54W and 68W, which correlates with our functional studies elucidating the profound HL of the last phase. On the other hand, OHCs showed a Cas-3 positive signal in 4W and 10W Kcnq4-/- mice, which could explain the mild HL of the first phase of DFNA2. IHCs did not show Cas-3 signal but they exhibited remarkable stereocilia defects by scanning microscopy, such as fusion and giant stereocilia in old mice. Collectively, these results are useful to understand the mechanisms involved in the human DFNA2. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/conferenceObject Reunión Book http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
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http://hdl.handle.net/11336/155864 Molecular mechanisms of cell death in a mouse model of progressive hearing loss; XXXV Annual Meeting of the Argentinian Society for Neuroscience Research; Buenos Aires; Argentina; 2020; 320-320 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/155864 |
identifier_str_mv |
Molecular mechanisms of cell death in a mouse model of progressive hearing loss; XXXV Annual Meeting of the Argentinian Society for Neuroscience Research; Buenos Aires; Argentina; 2020; 320-320 CONICET Digital CONICET |
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eng |
language |
eng |
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Sociedad Argentina de Investigación en Neurociencias |
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Sociedad Argentina de Investigación en Neurociencias |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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