Cargando…
Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea
In spiral ganglion neurons (SGNs), the afferent single units of the auditory nerve, high spontaneous and evoked firing rates ensure preservation of the temporal code describing the key features of incoming sound. During postnatal development, the spatiotemporal distribution of ion channel subtypes c...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684619/ https://www.ncbi.nlm.nih.gov/pubmed/29138759 http://dx.doi.org/10.1523/ENEURO.0303-17.2017 |
_version_ | 1783278518776365056 |
---|---|
author | Browne, Lorcan Smith, Katie E. Jagger, Daniel J. |
author_facet | Browne, Lorcan Smith, Katie E. Jagger, Daniel J. |
author_sort | Browne, Lorcan |
collection | PubMed |
description | In spiral ganglion neurons (SGNs), the afferent single units of the auditory nerve, high spontaneous and evoked firing rates ensure preservation of the temporal code describing the key features of incoming sound. During postnatal development, the spatiotemporal distribution of ion channel subtypes contributes to the maturation of action potential generation in SGNs, and to their ability to generate spike patterns that follow rapidly changing inputs. Here we describe tetrodotoxin (TTX)-sensitive Na(+) currents in SGNs cultured from mice, whose properties may support this fast spiking behavior. A subthreshold persistent Na(+) current (I(NaP)) and a resurgent Na(+) current (I(NaR)) both emerged prior to the onset of hearing and became more prevalent as hearing matured. Navβ4 subunits, which are proposed to play a key role in mediating I(NaR) elsewhere in the nervous system, were immunolocalized to the first heminode where spikes are generated in the auditory nerve, and to perisomatic nodes of Ranvier. ATX-II, a sea anemone toxin that slows classical Na(+) channel inactivation selectively, enhanced I(NaP) five-fold and I(NaR) three-fold in voltage clamp recordings. In rapidly-adapting SGNs under current clamp, ATX-II increased the likelihood of firing additional action potentials. The data identify I(NaP) and I(NaR) as novel regulators of excitability in SGNs, and consistent with their roles in other neuronal types, we suggest that these nonclassical Na(+) currents may contribute to the control of refractoriness in the auditory nerve. |
format | Online Article Text |
id | pubmed-5684619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-56846192017-11-14 Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea Browne, Lorcan Smith, Katie E. Jagger, Daniel J. eNeuro New Research In spiral ganglion neurons (SGNs), the afferent single units of the auditory nerve, high spontaneous and evoked firing rates ensure preservation of the temporal code describing the key features of incoming sound. During postnatal development, the spatiotemporal distribution of ion channel subtypes contributes to the maturation of action potential generation in SGNs, and to their ability to generate spike patterns that follow rapidly changing inputs. Here we describe tetrodotoxin (TTX)-sensitive Na(+) currents in SGNs cultured from mice, whose properties may support this fast spiking behavior. A subthreshold persistent Na(+) current (I(NaP)) and a resurgent Na(+) current (I(NaR)) both emerged prior to the onset of hearing and became more prevalent as hearing matured. Navβ4 subunits, which are proposed to play a key role in mediating I(NaR) elsewhere in the nervous system, were immunolocalized to the first heminode where spikes are generated in the auditory nerve, and to perisomatic nodes of Ranvier. ATX-II, a sea anemone toxin that slows classical Na(+) channel inactivation selectively, enhanced I(NaP) five-fold and I(NaR) three-fold in voltage clamp recordings. In rapidly-adapting SGNs under current clamp, ATX-II increased the likelihood of firing additional action potentials. The data identify I(NaP) and I(NaR) as novel regulators of excitability in SGNs, and consistent with their roles in other neuronal types, we suggest that these nonclassical Na(+) currents may contribute to the control of refractoriness in the auditory nerve. Society for Neuroscience 2017-11-14 /pmc/articles/PMC5684619/ /pubmed/29138759 http://dx.doi.org/10.1523/ENEURO.0303-17.2017 Text en Copyright © 2017 Browne et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | New Research Browne, Lorcan Smith, Katie E. Jagger, Daniel J. Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea |
title | Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea |
title_full | Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea |
title_fullStr | Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea |
title_full_unstemmed | Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea |
title_short | Identification of Persistent and Resurgent Sodium Currents in Spiral Ganglion Neurons Cultured from the Mouse Cochlea |
title_sort | identification of persistent and resurgent sodium currents in spiral ganglion neurons cultured from the mouse cochlea |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684619/ https://www.ncbi.nlm.nih.gov/pubmed/29138759 http://dx.doi.org/10.1523/ENEURO.0303-17.2017 |
work_keys_str_mv | AT brownelorcan identificationofpersistentandresurgentsodiumcurrentsinspiralganglionneuronsculturedfromthemousecochlea AT smithkatiee identificationofpersistentandresurgentsodiumcurrentsinspiralganglionneuronsculturedfromthemousecochlea AT jaggerdanielj identificationofpersistentandresurgentsodiumcurrentsinspiralganglionneuronsculturedfromthemousecochlea |