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Theoretical relation between axon initial segment geometry and excitability

In most vertebrate neurons, action potentials are triggered at the distal end of the axon initial segment (AIS). Both position and length of the AIS vary across and within neuron types, with activity, development and pathology. What is the impact of AIS geometry on excitability? Direct empirical ass...

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Detalles Bibliográficos
Autores principales: Goethals, Sarah, Brette, Romain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170651/
https://www.ncbi.nlm.nih.gov/pubmed/32223890
http://dx.doi.org/10.7554/eLife.53432
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author Goethals, Sarah
Brette, Romain
author_facet Goethals, Sarah
Brette, Romain
author_sort Goethals, Sarah
collection PubMed
description In most vertebrate neurons, action potentials are triggered at the distal end of the axon initial segment (AIS). Both position and length of the AIS vary across and within neuron types, with activity, development and pathology. What is the impact of AIS geometry on excitability? Direct empirical assessment has proven difficult because of the many potential confounding factors. Here, we carried a principled theoretical analysis to answer this question. We provide a simple formula relating AIS geometry and sodium conductance density to the somatic voltage threshold. A distal shift of the AIS normally produces a (modest) increase in excitability, but we explain how this pattern can reverse if a hyperpolarizing current is present at the AIS, due to resistive coupling with the soma. This work provides a theoretical tool to assess the significance of structural AIS plasticity for electrical function.
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spelling pubmed-71706512020-04-22 Theoretical relation between axon initial segment geometry and excitability Goethals, Sarah Brette, Romain eLife Computational and Systems Biology In most vertebrate neurons, action potentials are triggered at the distal end of the axon initial segment (AIS). Both position and length of the AIS vary across and within neuron types, with activity, development and pathology. What is the impact of AIS geometry on excitability? Direct empirical assessment has proven difficult because of the many potential confounding factors. Here, we carried a principled theoretical analysis to answer this question. We provide a simple formula relating AIS geometry and sodium conductance density to the somatic voltage threshold. A distal shift of the AIS normally produces a (modest) increase in excitability, but we explain how this pattern can reverse if a hyperpolarizing current is present at the AIS, due to resistive coupling with the soma. This work provides a theoretical tool to assess the significance of structural AIS plasticity for electrical function. eLife Sciences Publications, Ltd 2020-03-30 /pmc/articles/PMC7170651/ /pubmed/32223890 http://dx.doi.org/10.7554/eLife.53432 Text en © 2020, Goethals and Brette http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Goethals, Sarah
Brette, Romain
Theoretical relation between axon initial segment geometry and excitability
title Theoretical relation between axon initial segment geometry and excitability
title_full Theoretical relation between axon initial segment geometry and excitability
title_fullStr Theoretical relation between axon initial segment geometry and excitability
title_full_unstemmed Theoretical relation between axon initial segment geometry and excitability
title_short Theoretical relation between axon initial segment geometry and excitability
title_sort theoretical relation between axon initial segment geometry and excitability
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170651/
https://www.ncbi.nlm.nih.gov/pubmed/32223890
http://dx.doi.org/10.7554/eLife.53432
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