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FHF-independent conduction of action potentials along the leak-resistant cerebellar granule cell axon

Neurons in vertebrate central nervous systems initiate and conduct sodium action potentials in distinct subcellular compartments that differ architecturally and electrically. Here, we report several unanticipated passive and active properties of the cerebellar granule cell's unmyelinated axon....

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Autores principales: Dover, Katarzyna, Marra, Christopher, Solinas, Sergio, Popovic, Marko, Subramaniyam, Sathyaa, Zecevic, Dejan, D'Angelo, Egidio, Goldfarb, Mitchell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052690/
https://www.ncbi.nlm.nih.gov/pubmed/27666389
http://dx.doi.org/10.1038/ncomms12895
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author Dover, Katarzyna
Marra, Christopher
Solinas, Sergio
Popovic, Marko
Subramaniyam, Sathyaa
Zecevic, Dejan
D'Angelo, Egidio
Goldfarb, Mitchell
author_facet Dover, Katarzyna
Marra, Christopher
Solinas, Sergio
Popovic, Marko
Subramaniyam, Sathyaa
Zecevic, Dejan
D'Angelo, Egidio
Goldfarb, Mitchell
author_sort Dover, Katarzyna
collection PubMed
description Neurons in vertebrate central nervous systems initiate and conduct sodium action potentials in distinct subcellular compartments that differ architecturally and electrically. Here, we report several unanticipated passive and active properties of the cerebellar granule cell's unmyelinated axon. Whereas spike initiation at the axon initial segment relies on sodium channel (Na(v))-associated fibroblast growth factor homologous factor (FHF) proteins to delay Na(v) inactivation, distal axonal Na(v)s show little FHF association or FHF requirement for high-frequency transmission, velocity and waveforms of conducting action potentials. In addition, leak conductance density along the distal axon is estimated as <1% that of somatodendritic membrane. The faster inactivation rate of FHF-free Na(v)s together with very low axonal leak conductance serves to minimize ionic fluxes and energetic demand during repetitive spike conduction and at rest. The absence of FHFs from Na(v)s at nodes of Ranvier in the central nervous system suggests a similar mechanism of current flux minimization along myelinated axons.
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spelling pubmed-50526902016-10-21 FHF-independent conduction of action potentials along the leak-resistant cerebellar granule cell axon Dover, Katarzyna Marra, Christopher Solinas, Sergio Popovic, Marko Subramaniyam, Sathyaa Zecevic, Dejan D'Angelo, Egidio Goldfarb, Mitchell Nat Commun Article Neurons in vertebrate central nervous systems initiate and conduct sodium action potentials in distinct subcellular compartments that differ architecturally and electrically. Here, we report several unanticipated passive and active properties of the cerebellar granule cell's unmyelinated axon. Whereas spike initiation at the axon initial segment relies on sodium channel (Na(v))-associated fibroblast growth factor homologous factor (FHF) proteins to delay Na(v) inactivation, distal axonal Na(v)s show little FHF association or FHF requirement for high-frequency transmission, velocity and waveforms of conducting action potentials. In addition, leak conductance density along the distal axon is estimated as <1% that of somatodendritic membrane. The faster inactivation rate of FHF-free Na(v)s together with very low axonal leak conductance serves to minimize ionic fluxes and energetic demand during repetitive spike conduction and at rest. The absence of FHFs from Na(v)s at nodes of Ranvier in the central nervous system suggests a similar mechanism of current flux minimization along myelinated axons. Nature Publishing Group 2016-09-26 /pmc/articles/PMC5052690/ /pubmed/27666389 http://dx.doi.org/10.1038/ncomms12895 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Dover, Katarzyna
Marra, Christopher
Solinas, Sergio
Popovic, Marko
Subramaniyam, Sathyaa
Zecevic, Dejan
D'Angelo, Egidio
Goldfarb, Mitchell
FHF-independent conduction of action potentials along the leak-resistant cerebellar granule cell axon
title FHF-independent conduction of action potentials along the leak-resistant cerebellar granule cell axon
title_full FHF-independent conduction of action potentials along the leak-resistant cerebellar granule cell axon
title_fullStr FHF-independent conduction of action potentials along the leak-resistant cerebellar granule cell axon
title_full_unstemmed FHF-independent conduction of action potentials along the leak-resistant cerebellar granule cell axon
title_short FHF-independent conduction of action potentials along the leak-resistant cerebellar granule cell axon
title_sort fhf-independent conduction of action potentials along the leak-resistant cerebellar granule cell axon
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052690/
https://www.ncbi.nlm.nih.gov/pubmed/27666389
http://dx.doi.org/10.1038/ncomms12895
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