Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development

Autores
Castagnola, Tais; Katz, Eleonora; Elgoyhen, Ana Belen; Goutman, Juan Diego; Wedemeyer, Carolina
Año de publicación
2023
Idioma
inglés
Tipo de recurso
documento de conferencia
Estado
versión publicada
Descripción
During development, inner hair cells (IHCs) in the mammalian cochlea are unresponsive to acoustic stimuli but instead present intrinsic electrical activity, crucial for the normal development of the auditory pathway. During this same period, neurons originating from the medial olivocochlear complex (MOC) transiently innervate the soma of IHCs. This synapse is mediated by acetylcholine (ACh), activating nicotinic receptors assembled by alpha9 and alpha10 subunits and ultimately controlling IHC excitability. Although it is a cholinergic synapse, previous evidence indicated the presence of abundant GABA and presynaptic GABAB receptors (GABAB-R). Moreover, application of GABAB-R agonists generated a reduction in ACh release. Transgenic Chat tm2(crc)Lowl/J-Cre (ChAT-cre) and Gad2 tm1(cre/ERT2)Zjh/J-Cre (GAD2-cre) mice of either sex were mated with a floxed channel rhodopsin 2 (ChR2) line, Ai32, to drive specific ChR2 expression. Whole cell patch clamp was performed in P9-11 IHCs while either cholinergic (ChATCre/ ChR2) or GABAergic (GAD2-Cre/ChR2) fibers were optogenetically stimulated. Additionally, immunohistochemistry techniques were used to characterize cholinergic and GABAergic expression in B6.Cg-Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/J (tdTomato) crossed with GAD2-Cre. Furthermore, we performed calcium imaging experiments at the same age range on Balb-C mice. For this, IHCs were dialyzed with a fluorescent calcium indicator (Fluo 4) and MOC electrically stimulated during the application of a GABAB-R antagonist (CGP 36216, 200 μM). Firstly, eIPSCs were optogenetically triggered in ChAT-cre/ChR2 mice, and these responses could be partially blocked with alpha-bungarotoxin (60.8 ± 4.4%, N=5). Optogenetic experiments were also performed in GAD2-cre/ChR2 mice producing eIPSC that could also be blocked by alpha-bungarotoxin (82.3 ± 7.2%, N=4). This result strongly suggests that a cholinergic response could be elicited in IHC in GAD-expressing neurons. Also, immunohistochemistry experiments done at the base of IHCs showed approximately 30% co-localization of GABAergic and cholinergic labelling. Finally, calcium imaging experiments were performed with stimulation of MOC fibers, allowing us to resolve the activation of single synaptic sites. The application of the GABAB-R antagonist, CGP 36216, produced an increase in the activation probability of individual calcium hotspots in the context of heterogeneous responses in different sites of a single IHC. In conclusion, here we provide evidence suggesting that GABA and ACh could be co-released from MOC terminals. Whereas ACh acts postsynaptically activating α9α10 receptors, the role of GABA is presynaptic, as a negative feedback signal to locally regulate cholinergic inhibition of IHCs. Calcium imaging experiments suggest that GABA modulation operates differently at each synaptic site.
Fil: Castagnola, Tais. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Katz, Eleonora. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Elgoyhen, Ana Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Farmacologia; Argentina
Fil: Goutman, Juan Diego. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Wedemeyer, Carolina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
ARO 46th Annual Midwinter Meeting
Orlando
Estados Unidos
Association for Research in Otorrinolaringology
Materia
COCHLEA
OPTOGENETIC
CALCIUM IMAGING
OLIVOCOCHLEAR
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/231945

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oai_identifier_str oai:ri.conicet.gov.ar:11336/231945
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During DevelopmentCastagnola, TaisKatz, EleonoraElgoyhen, Ana BelenGoutman, Juan DiegoWedemeyer, CarolinaCOCHLEAOPTOGENETICCALCIUM IMAGINGOLIVOCOCHLEARhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1During development, inner hair cells (IHCs) in the mammalian cochlea are unresponsive to acoustic stimuli but instead present intrinsic electrical activity, crucial for the normal development of the auditory pathway. During this same period, neurons originating from the medial olivocochlear complex (MOC) transiently innervate the soma of IHCs. This synapse is mediated by acetylcholine (ACh), activating nicotinic receptors assembled by alpha9 and alpha10 subunits and ultimately controlling IHC excitability. Although it is a cholinergic synapse, previous evidence indicated the presence of abundant GABA and presynaptic GABAB receptors (GABAB-R). Moreover, application of GABAB-R agonists generated a reduction in ACh release. Transgenic Chat tm2(crc)Lowl/J-Cre (ChAT-cre) and Gad2 tm1(cre/ERT2)Zjh/J-Cre (GAD2-cre) mice of either sex were mated with a floxed channel rhodopsin 2 (ChR2) line, Ai32, to drive specific ChR2 expression. Whole cell patch clamp was performed in P9-11 IHCs while either cholinergic (ChATCre/ ChR2) or GABAergic (GAD2-Cre/ChR2) fibers were optogenetically stimulated. Additionally, immunohistochemistry techniques were used to characterize cholinergic and GABAergic expression in B6.Cg-Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/J (tdTomato) crossed with GAD2-Cre. Furthermore, we performed calcium imaging experiments at the same age range on Balb-C mice. For this, IHCs were dialyzed with a fluorescent calcium indicator (Fluo 4) and MOC electrically stimulated during the application of a GABAB-R antagonist (CGP 36216, 200 μM). Firstly, eIPSCs were optogenetically triggered in ChAT-cre/ChR2 mice, and these responses could be partially blocked with alpha-bungarotoxin (60.8 ± 4.4%, N=5). Optogenetic experiments were also performed in GAD2-cre/ChR2 mice producing eIPSC that could also be blocked by alpha-bungarotoxin (82.3 ± 7.2%, N=4). This result strongly suggests that a cholinergic response could be elicited in IHC in GAD-expressing neurons. Also, immunohistochemistry experiments done at the base of IHCs showed approximately 30% co-localization of GABAergic and cholinergic labelling. Finally, calcium imaging experiments were performed with stimulation of MOC fibers, allowing us to resolve the activation of single synaptic sites. The application of the GABAB-R antagonist, CGP 36216, produced an increase in the activation probability of individual calcium hotspots in the context of heterogeneous responses in different sites of a single IHC. In conclusion, here we provide evidence suggesting that GABA and ACh could be co-released from MOC terminals. Whereas ACh acts postsynaptically activating α9α10 receptors, the role of GABA is presynaptic, as a negative feedback signal to locally regulate cholinergic inhibition of IHCs. Calcium imaging experiments suggest that GABA modulation operates differently at each synaptic site.Fil: Castagnola, Tais. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Katz, Eleonora. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Elgoyhen, Ana Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Farmacologia; ArgentinaFil: Goutman, Juan Diego. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Wedemeyer, Carolina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaARO 46th Annual Midwinter MeetingOrlandoEstados UnidosAssociation for Research in OtorrinolaringologyAssociation for Research in Otorrinolaringology2023info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectCongresoBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/231945Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development; ARO 46th Annual Midwinter Meeting; Orlando; Estados Unidos; 2023; 1-1CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://aro.org/wp-content/uploads/2023/02/Abstract_Book_COMBINED_2.20.23.pdfInternacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:44:34Zoai:ri.conicet.gov.ar:11336/231945instacron: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:34982025-09-29 09:44:34.533CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development
title Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development
spellingShingle Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development
Castagnola, Tais
COCHLEA
OPTOGENETIC
CALCIUM IMAGING
OLIVOCOCHLEAR
title_short Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development
title_full Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development
title_fullStr Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development
title_full_unstemmed Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development
title_sort Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development
dc.creator.none.fl_str_mv Castagnola, Tais
Katz, Eleonora
Elgoyhen, Ana Belen
Goutman, Juan Diego
Wedemeyer, Carolina
author Castagnola, Tais
author_facet Castagnola, Tais
Katz, Eleonora
Elgoyhen, Ana Belen
Goutman, Juan Diego
Wedemeyer, Carolina
author_role author
author2 Katz, Eleonora
Elgoyhen, Ana Belen
Goutman, Juan Diego
Wedemeyer, Carolina
author2_role author
author
author
author
dc.subject.none.fl_str_mv COCHLEA
OPTOGENETIC
CALCIUM IMAGING
OLIVOCOCHLEAR
topic COCHLEA
OPTOGENETIC
CALCIUM IMAGING
OLIVOCOCHLEAR
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv During development, inner hair cells (IHCs) in the mammalian cochlea are unresponsive to acoustic stimuli but instead present intrinsic electrical activity, crucial for the normal development of the auditory pathway. During this same period, neurons originating from the medial olivocochlear complex (MOC) transiently innervate the soma of IHCs. This synapse is mediated by acetylcholine (ACh), activating nicotinic receptors assembled by alpha9 and alpha10 subunits and ultimately controlling IHC excitability. Although it is a cholinergic synapse, previous evidence indicated the presence of abundant GABA and presynaptic GABAB receptors (GABAB-R). Moreover, application of GABAB-R agonists generated a reduction in ACh release. Transgenic Chat tm2(crc)Lowl/J-Cre (ChAT-cre) and Gad2 tm1(cre/ERT2)Zjh/J-Cre (GAD2-cre) mice of either sex were mated with a floxed channel rhodopsin 2 (ChR2) line, Ai32, to drive specific ChR2 expression. Whole cell patch clamp was performed in P9-11 IHCs while either cholinergic (ChATCre/ ChR2) or GABAergic (GAD2-Cre/ChR2) fibers were optogenetically stimulated. Additionally, immunohistochemistry techniques were used to characterize cholinergic and GABAergic expression in B6.Cg-Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/J (tdTomato) crossed with GAD2-Cre. Furthermore, we performed calcium imaging experiments at the same age range on Balb-C mice. For this, IHCs were dialyzed with a fluorescent calcium indicator (Fluo 4) and MOC electrically stimulated during the application of a GABAB-R antagonist (CGP 36216, 200 μM). Firstly, eIPSCs were optogenetically triggered in ChAT-cre/ChR2 mice, and these responses could be partially blocked with alpha-bungarotoxin (60.8 ± 4.4%, N=5). Optogenetic experiments were also performed in GAD2-cre/ChR2 mice producing eIPSC that could also be blocked by alpha-bungarotoxin (82.3 ± 7.2%, N=4). This result strongly suggests that a cholinergic response could be elicited in IHC in GAD-expressing neurons. Also, immunohistochemistry experiments done at the base of IHCs showed approximately 30% co-localization of GABAergic and cholinergic labelling. Finally, calcium imaging experiments were performed with stimulation of MOC fibers, allowing us to resolve the activation of single synaptic sites. The application of the GABAB-R antagonist, CGP 36216, produced an increase in the activation probability of individual calcium hotspots in the context of heterogeneous responses in different sites of a single IHC. In conclusion, here we provide evidence suggesting that GABA and ACh could be co-released from MOC terminals. Whereas ACh acts postsynaptically activating α9α10 receptors, the role of GABA is presynaptic, as a negative feedback signal to locally regulate cholinergic inhibition of IHCs. Calcium imaging experiments suggest that GABA modulation operates differently at each synaptic site.
Fil: Castagnola, Tais. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Katz, Eleonora. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Elgoyhen, Ana Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Farmacologia; Argentina
Fil: Goutman, Juan Diego. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Wedemeyer, Carolina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
ARO 46th Annual Midwinter Meeting
Orlando
Estados Unidos
Association for Research in Otorrinolaringology
description During development, inner hair cells (IHCs) in the mammalian cochlea are unresponsive to acoustic stimuli but instead present intrinsic electrical activity, crucial for the normal development of the auditory pathway. During this same period, neurons originating from the medial olivocochlear complex (MOC) transiently innervate the soma of IHCs. This synapse is mediated by acetylcholine (ACh), activating nicotinic receptors assembled by alpha9 and alpha10 subunits and ultimately controlling IHC excitability. Although it is a cholinergic synapse, previous evidence indicated the presence of abundant GABA and presynaptic GABAB receptors (GABAB-R). Moreover, application of GABAB-R agonists generated a reduction in ACh release. Transgenic Chat tm2(crc)Lowl/J-Cre (ChAT-cre) and Gad2 tm1(cre/ERT2)Zjh/J-Cre (GAD2-cre) mice of either sex were mated with a floxed channel rhodopsin 2 (ChR2) line, Ai32, to drive specific ChR2 expression. Whole cell patch clamp was performed in P9-11 IHCs while either cholinergic (ChATCre/ ChR2) or GABAergic (GAD2-Cre/ChR2) fibers were optogenetically stimulated. Additionally, immunohistochemistry techniques were used to characterize cholinergic and GABAergic expression in B6.Cg-Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/J (tdTomato) crossed with GAD2-Cre. Furthermore, we performed calcium imaging experiments at the same age range on Balb-C mice. For this, IHCs were dialyzed with a fluorescent calcium indicator (Fluo 4) and MOC electrically stimulated during the application of a GABAB-R antagonist (CGP 36216, 200 μM). Firstly, eIPSCs were optogenetically triggered in ChAT-cre/ChR2 mice, and these responses could be partially blocked with alpha-bungarotoxin (60.8 ± 4.4%, N=5). Optogenetic experiments were also performed in GAD2-cre/ChR2 mice producing eIPSC that could also be blocked by alpha-bungarotoxin (82.3 ± 7.2%, N=4). This result strongly suggests that a cholinergic response could be elicited in IHC in GAD-expressing neurons. Also, immunohistochemistry experiments done at the base of IHCs showed approximately 30% co-localization of GABAergic and cholinergic labelling. Finally, calcium imaging experiments were performed with stimulation of MOC fibers, allowing us to resolve the activation of single synaptic sites. The application of the GABAB-R antagonist, CGP 36216, produced an increase in the activation probability of individual calcium hotspots in the context of heterogeneous responses in different sites of a single IHC. In conclusion, here we provide evidence suggesting that GABA and ACh could be co-released from MOC terminals. Whereas ACh acts postsynaptically activating α9α10 receptors, the role of GABA is presynaptic, as a negative feedback signal to locally regulate cholinergic inhibition of IHCs. Calcium imaging experiments suggest that GABA modulation operates differently at each synaptic site.
publishDate 2023
dc.date.none.fl_str_mv 2023
dc.type.none.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/conferenceObject
Congreso
Book
http://purl.org/coar/resource_type/c_5794
info:ar-repo/semantics/documentoDeConferencia
status_str publishedVersion
format conferenceObject
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/231945
Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development; ARO 46th Annual Midwinter Meeting; Orlando; Estados Unidos; 2023; 1-1
CONICET Digital
CONICET
url http://hdl.handle.net/11336/231945
identifier_str_mv Co-Release of GABA and ACh from Medial Olivocochlear Efferent Fibers During Development; ARO 46th Annual Midwinter Meeting; Orlando; Estados Unidos; 2023; 1-1
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://aro.org/wp-content/uploads/2023/02/Abstract_Book_COMBINED_2.20.23.pdf
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
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application/pdf
application/pdf
dc.coverage.none.fl_str_mv Internacional
dc.publisher.none.fl_str_mv Association for Research in Otorrinolaringology
publisher.none.fl_str_mv Association for Research in Otorrinolaringology
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
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reponame_str CONICET Digital (CONICET)
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instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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