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
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/87276
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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 |
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SEDICI (UNLP) |
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Universidad Nacional de La Plata |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
repository.mail.fl_str_mv |
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