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Developmental Profile of Ion Channel Specializations in the Avian Nucleus Magnocellularis

Ultrafast and temporally precise action potentials (APs) are biophysical specializations of auditory brainstem neurons; properties necessary for encoding sound localization and communication cues. Fundamental to these specializations are voltage dependent potassium (K(V)) and sodium (Na(V)) ion chan...

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Autores principales: Hong, Hui, Rollman, Lisia, Feinstein, Brooke, Sanchez, Jason Tait
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811932/
https://www.ncbi.nlm.nih.gov/pubmed/27065805
http://dx.doi.org/10.3389/fncel.2016.00080
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author Hong, Hui
Rollman, Lisia
Feinstein, Brooke
Sanchez, Jason Tait
author_facet Hong, Hui
Rollman, Lisia
Feinstein, Brooke
Sanchez, Jason Tait
author_sort Hong, Hui
collection PubMed
description Ultrafast and temporally precise action potentials (APs) are biophysical specializations of auditory brainstem neurons; properties necessary for encoding sound localization and communication cues. Fundamental to these specializations are voltage dependent potassium (K(V)) and sodium (Na(V)) ion channels. Here, we characterized the functional development of these ion channels and quantified how they shape AP properties in the avian cochlear nucleus magnocellularis (NM). We report that late developing NM neurons (embryonic [E] days 19–21) generate fast APs that reliably phase lock to sinusoidal inputs at 75 Hz. In contrast, early developing neurons (<E12) have slower and less reliable APs that preferentially fire to lower frequencies (5–10 Hz). With development, the membrane time constant of NM neurons became faster, while input resistance and capacitance decreased. Change in input resistance was due to a 2-fold increase in K(V) current from E10 to E21 and when high-voltage activated potassium (K(+)(HVA)) channels were blocked, APs for all ages became significantly slower. This was most evident for early developing neurons where the ratio of K(+)(HVA) current accounted for ~85% of the total K(V) response. This ratio dropped to ~50% for late developing neurons, suggesting a developmental upregulation of low-voltage activated potassium (K(+)(LVA)) channels. Indeed, blockade of K(+)(LVA) eliminated remaining current and increased neural excitability for late developing neurons. We also report developmental changes in the amplitude, kinetics and voltage dependence of Na(V) currents. For early developing neurons, increase in Na(V) current amplitude was due to channel density while channel conductance dominated for late developing neurons. From E10 to E21, Na(V) channel currents became faster but differed in their voltage dependence; early developing neurons (<E16) had similar Na(V) channel inactivation voltages while late developing NM neurons (>E19) contained Na(V) channels that inactivate at more negative voltages, suggesting alterations in Na(V) channel subtypes. Taken together, our results indicate that the refinement of passive and active ion channel properties operate differentially in order to develop fast and reliable APs in the avian NM.
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spelling pubmed-48119322016-04-08 Developmental Profile of Ion Channel Specializations in the Avian Nucleus Magnocellularis Hong, Hui Rollman, Lisia Feinstein, Brooke Sanchez, Jason Tait Front Cell Neurosci Neuroscience Ultrafast and temporally precise action potentials (APs) are biophysical specializations of auditory brainstem neurons; properties necessary for encoding sound localization and communication cues. Fundamental to these specializations are voltage dependent potassium (K(V)) and sodium (Na(V)) ion channels. Here, we characterized the functional development of these ion channels and quantified how they shape AP properties in the avian cochlear nucleus magnocellularis (NM). We report that late developing NM neurons (embryonic [E] days 19–21) generate fast APs that reliably phase lock to sinusoidal inputs at 75 Hz. In contrast, early developing neurons (<E12) have slower and less reliable APs that preferentially fire to lower frequencies (5–10 Hz). With development, the membrane time constant of NM neurons became faster, while input resistance and capacitance decreased. Change in input resistance was due to a 2-fold increase in K(V) current from E10 to E21 and when high-voltage activated potassium (K(+)(HVA)) channels were blocked, APs for all ages became significantly slower. This was most evident for early developing neurons where the ratio of K(+)(HVA) current accounted for ~85% of the total K(V) response. This ratio dropped to ~50% for late developing neurons, suggesting a developmental upregulation of low-voltage activated potassium (K(+)(LVA)) channels. Indeed, blockade of K(+)(LVA) eliminated remaining current and increased neural excitability for late developing neurons. We also report developmental changes in the amplitude, kinetics and voltage dependence of Na(V) currents. For early developing neurons, increase in Na(V) current amplitude was due to channel density while channel conductance dominated for late developing neurons. From E10 to E21, Na(V) channel currents became faster but differed in their voltage dependence; early developing neurons (<E16) had similar Na(V) channel inactivation voltages while late developing NM neurons (>E19) contained Na(V) channels that inactivate at more negative voltages, suggesting alterations in Na(V) channel subtypes. Taken together, our results indicate that the refinement of passive and active ion channel properties operate differentially in order to develop fast and reliable APs in the avian NM. Frontiers Media S.A. 2016-03-30 /pmc/articles/PMC4811932/ /pubmed/27065805 http://dx.doi.org/10.3389/fncel.2016.00080 Text en Copyright © 2016 Hong, Rollman, Feinstein and Sanchez. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Hong, Hui
Rollman, Lisia
Feinstein, Brooke
Sanchez, Jason Tait
Developmental Profile of Ion Channel Specializations in the Avian Nucleus Magnocellularis
title Developmental Profile of Ion Channel Specializations in the Avian Nucleus Magnocellularis
title_full Developmental Profile of Ion Channel Specializations in the Avian Nucleus Magnocellularis
title_fullStr Developmental Profile of Ion Channel Specializations in the Avian Nucleus Magnocellularis
title_full_unstemmed Developmental Profile of Ion Channel Specializations in the Avian Nucleus Magnocellularis
title_short Developmental Profile of Ion Channel Specializations in the Avian Nucleus Magnocellularis
title_sort developmental profile of ion channel specializations in the avian nucleus magnocellularis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811932/
https://www.ncbi.nlm.nih.gov/pubmed/27065805
http://dx.doi.org/10.3389/fncel.2016.00080
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