An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cells

Autores
Spaiardi, Pablo; Tavazzani, Elisa; Manca, Marco; Milesi, Verónica; Russo, Giancarlo; Prigioni, Ivo; Marcotti, Walter; Magistretti, Jacopo; Masetto, Sergio
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Type I and type II hair cells are the sensory receptors of the mammalian vestibular epithelia. Type I hair cells are characterized by their basolateral membrane being enveloped in a single large afferent nerve terminal, named the calyx, and by the expression of a low-voltage-activated outward rectifying K+ current, IK,L. The biophysical properties and molecular profile of IK,L are still largely unknown. By using the patch-clamp whole-cell technique, we examined the voltage- and time-dependent properties of IK,L in type I hair cells of the mouse semicircular canal. We found that the biophysical properties of IK,L were affected by an unstable K+ equilibrium potential (VeqK+). Both the outward and inward K+ currents shifted VeqK+ consistent with K+ accumulation or depletion, respectively, in the extracellular space, which we attributed to a residual calyx attached to the basolateral membrane of the hair cells. We therefore optimized the hair cell dissociation protocol in order to isolate mature type I hair cells without their calyx. In these cells, the uncontaminated IK,L showed a half-activation at –79.6 mV and a steep voltage dependence (2.8 mV). IK,L also showed complex activation and deactivation kinetics, which we faithfully reproduced by an allosteric channel gating scheme where the channel is able to open from all (five) closed states. The ‘early’ open states substantially contribute to IK,L activation at negative voltages. This study provides the first complete description of the ‘native’ biophysical properties of IK,L in adult mouse vestibular type I hair cells.
Instituto de Estudios Inmunológicos y Fisiopatológicos
Facultad de Ciencias Exactas
Materia
Ciencias Exactas
channel gating model
IK,L
type I vestibular hair cell
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/87276

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repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cellsSpaiardi, PabloTavazzani, ElisaManca, MarcoMilesi, VerónicaRusso, GiancarloPrigioni, IvoMarcotti, WalterMagistretti, JacopoMasetto, SergioCiencias Exactaschannel gating modelIK,Ltype I vestibular hair cellType I and type II hair cells are the sensory receptors of the mammalian vestibular epithelia. Type I hair cells are characterized by their basolateral membrane being enveloped in a single large afferent nerve terminal, named the calyx, and by the expression of a low-voltage-activated outward rectifying K<sup>+</sup> current, I<sub>K,L</sub>. The biophysical properties and molecular profile of I<sub>K,L</sub> are still largely unknown. By using the patch-clamp whole-cell technique, we examined the voltage- and time-dependent properties of I<sub>K,L</sub> in type I hair cells of the mouse semicircular canal. We found that the biophysical properties of I<sub>K,L</sub> were affected by an unstable K<sup>+</sup> equilibrium potential (V<sub>eq</sub>K<sup>+</sup>). Both the outward and inward K<sup>+</sup> currents shifted V<sub>eq</sub>K<sup>+</sup> consistent with K<sup>+</sup> accumulation or depletion, respectively, in the extracellular space, which we attributed to a residual calyx attached to the basolateral membrane of the hair cells. We therefore optimized the hair cell dissociation protocol in order to isolate mature type I hair cells without their calyx. In these cells, the uncontaminated I<sub>K,L</sub> showed a half-activation at –79.6 mV and a steep voltage dependence (2.8 mV). I<sub>K,L</sub> also showed complex activation and deactivation kinetics, which we faithfully reproduced by an allosteric channel gating scheme where the channel is able to open from all (five) closed states. The ‘early’ open states substantially contribute to I<sub>K,L</sub> activation at negative voltages. This study provides the first complete description of the ‘native’ biophysical properties of I<sub>K,L</sub> in adult mouse vestibular type I hair cells.Instituto de Estudios Inmunológicos y FisiopatológicosFacultad de Ciencias Exactas2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf6735-6750http://sedici.unlp.edu.ar/handle/10915/87276enginfo:eu-repo/semantics/altIdentifier/issn/0022-3751info:eu-repo/semantics/altIdentifier/doi/10.1113/JP274202info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:17:09Zoai:sedici.unlp.edu.ar:10915/87276Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:17:10.259SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cells
title An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cells
spellingShingle An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cells
Spaiardi, Pablo
Ciencias Exactas
channel gating model
IK,L
type I vestibular hair cell
title_short An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cells
title_full An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cells
title_fullStr An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cells
title_full_unstemmed An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cells
title_sort An allosteric gating model recapitulates the biophysical properties of I<sub>K,L</sub> expressed in mouse vestibular type I hair cells
dc.creator.none.fl_str_mv Spaiardi, Pablo
Tavazzani, Elisa
Manca, Marco
Milesi, Verónica
Russo, Giancarlo
Prigioni, Ivo
Marcotti, Walter
Magistretti, Jacopo
Masetto, Sergio
author Spaiardi, Pablo
author_facet Spaiardi, Pablo
Tavazzani, Elisa
Manca, Marco
Milesi, Verónica
Russo, Giancarlo
Prigioni, Ivo
Marcotti, Walter
Magistretti, Jacopo
Masetto, Sergio
author_role author
author2 Tavazzani, Elisa
Manca, Marco
Milesi, Verónica
Russo, Giancarlo
Prigioni, Ivo
Marcotti, Walter
Magistretti, Jacopo
Masetto, Sergio
author2_role author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
channel gating model
IK,L
type I vestibular hair cell
topic Ciencias Exactas
channel gating model
IK,L
type I vestibular hair cell
dc.description.none.fl_txt_mv Type I and type II hair cells are the sensory receptors of the mammalian vestibular epithelia. Type I hair cells are characterized by their basolateral membrane being enveloped in a single large afferent nerve terminal, named the calyx, and by the expression of a low-voltage-activated outward rectifying K<sup>+</sup> current, I<sub>K,L</sub>. The biophysical properties and molecular profile of I<sub>K,L</sub> are still largely unknown. By using the patch-clamp whole-cell technique, we examined the voltage- and time-dependent properties of I<sub>K,L</sub> in type I hair cells of the mouse semicircular canal. We found that the biophysical properties of I<sub>K,L</sub> were affected by an unstable K<sup>+</sup> equilibrium potential (V<sub>eq</sub>K<sup>+</sup>). Both the outward and inward K<sup>+</sup> currents shifted V<sub>eq</sub>K<sup>+</sup> consistent with K<sup>+</sup> accumulation or depletion, respectively, in the extracellular space, which we attributed to a residual calyx attached to the basolateral membrane of the hair cells. We therefore optimized the hair cell dissociation protocol in order to isolate mature type I hair cells without their calyx. In these cells, the uncontaminated I<sub>K,L</sub> showed a half-activation at –79.6 mV and a steep voltage dependence (2.8 mV). I<sub>K,L</sub> also showed complex activation and deactivation kinetics, which we faithfully reproduced by an allosteric channel gating scheme where the channel is able to open from all (five) closed states. The ‘early’ open states substantially contribute to I<sub>K,L</sub> activation at negative voltages. This study provides the first complete description of the ‘native’ biophysical properties of I<sub>K,L</sub> in adult mouse vestibular type I hair cells.
Instituto de Estudios Inmunológicos y Fisiopatológicos
Facultad de Ciencias Exactas
description Type I and type II hair cells are the sensory receptors of the mammalian vestibular epithelia. Type I hair cells are characterized by their basolateral membrane being enveloped in a single large afferent nerve terminal, named the calyx, and by the expression of a low-voltage-activated outward rectifying K<sup>+</sup> current, I<sub>K,L</sub>. The biophysical properties and molecular profile of I<sub>K,L</sub> are still largely unknown. By using the patch-clamp whole-cell technique, we examined the voltage- and time-dependent properties of I<sub>K,L</sub> in type I hair cells of the mouse semicircular canal. We found that the biophysical properties of I<sub>K,L</sub> were affected by an unstable K<sup>+</sup> equilibrium potential (V<sub>eq</sub>K<sup>+</sup>). Both the outward and inward K<sup>+</sup> currents shifted V<sub>eq</sub>K<sup>+</sup> consistent with K<sup>+</sup> accumulation or depletion, respectively, in the extracellular space, which we attributed to a residual calyx attached to the basolateral membrane of the hair cells. We therefore optimized the hair cell dissociation protocol in order to isolate mature type I hair cells without their calyx. In these cells, the uncontaminated I<sub>K,L</sub> showed a half-activation at –79.6 mV and a steep voltage dependence (2.8 mV). I<sub>K,L</sub> also showed complex activation and deactivation kinetics, which we faithfully reproduced by an allosteric channel gating scheme where the channel is able to open from all (five) closed states. The ‘early’ open states substantially contribute to I<sub>K,L</sub> activation at negative voltages. This study provides the first complete description of the ‘native’ biophysical properties of I<sub>K,L</sub> in adult mouse vestibular type I hair cells.
publishDate 2017
dc.date.none.fl_str_mv 2017
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
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/87276
url http://sedici.unlp.edu.ar/handle/10915/87276
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0022-3751
info:eu-repo/semantics/altIdentifier/doi/10.1113/JP274202
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.format.none.fl_str_mv application/pdf
6735-6750
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
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