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Axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering

While axon fasciculation plays a key role in the development of neural networks, very little is known about its dynamics and the underlying biophysical mechanisms. In a model system composed of neurons grown ex vivo from explants of embryonic mouse olfactory epithelia, we observed that axons dynamic...

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Autores principales: Šmít, Daniel, Fouquet, Coralie, Pincet, Frédéric, Zapotocky, Martin, Trembleau, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478281/
https://www.ncbi.nlm.nih.gov/pubmed/28422009
http://dx.doi.org/10.7554/eLife.19907
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author Šmít, Daniel
Fouquet, Coralie
Pincet, Frédéric
Zapotocky, Martin
Trembleau, Alain
author_facet Šmít, Daniel
Fouquet, Coralie
Pincet, Frédéric
Zapotocky, Martin
Trembleau, Alain
author_sort Šmít, Daniel
collection PubMed
description While axon fasciculation plays a key role in the development of neural networks, very little is known about its dynamics and the underlying biophysical mechanisms. In a model system composed of neurons grown ex vivo from explants of embryonic mouse olfactory epithelia, we observed that axons dynamically interact with each other through their shafts, leading to zippering and unzippering behavior that regulates their fasciculation. Taking advantage of this new preparation suitable for studying such interactions, we carried out a detailed biophysical analysis of zippering, occurring either spontaneously or induced by micromanipulations and pharmacological treatments. We show that zippering arises from the competition of axon-axon adhesion and mechanical tension in the axons, and provide the first quantification of the force of axon-axon adhesion. Furthermore, we introduce a biophysical model of the zippering dynamics, and we quantitatively relate the individual zipper properties to global characteristics of the developing axon network. Our study uncovers a new role of mechanical tension in neural development: the regulation of axon fasciculation. DOI: http://dx.doi.org/10.7554/eLife.19907.001
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spelling pubmed-54782812017-06-22 Axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering Šmít, Daniel Fouquet, Coralie Pincet, Frédéric Zapotocky, Martin Trembleau, Alain eLife Biophysics and Structural Biology While axon fasciculation plays a key role in the development of neural networks, very little is known about its dynamics and the underlying biophysical mechanisms. In a model system composed of neurons grown ex vivo from explants of embryonic mouse olfactory epithelia, we observed that axons dynamically interact with each other through their shafts, leading to zippering and unzippering behavior that regulates their fasciculation. Taking advantage of this new preparation suitable for studying such interactions, we carried out a detailed biophysical analysis of zippering, occurring either spontaneously or induced by micromanipulations and pharmacological treatments. We show that zippering arises from the competition of axon-axon adhesion and mechanical tension in the axons, and provide the first quantification of the force of axon-axon adhesion. Furthermore, we introduce a biophysical model of the zippering dynamics, and we quantitatively relate the individual zipper properties to global characteristics of the developing axon network. Our study uncovers a new role of mechanical tension in neural development: the regulation of axon fasciculation. DOI: http://dx.doi.org/10.7554/eLife.19907.001 eLife Sciences Publications, Ltd 2017-04-19 /pmc/articles/PMC5478281/ /pubmed/28422009 http://dx.doi.org/10.7554/eLife.19907 Text en © 2017, Šmít et al 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 Biophysics and Structural Biology
Šmít, Daniel
Fouquet, Coralie
Pincet, Frédéric
Zapotocky, Martin
Trembleau, Alain
Axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering
title Axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering
title_full Axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering
title_fullStr Axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering
title_full_unstemmed Axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering
title_short Axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering
title_sort axon tension regulates fasciculation/defasciculation through the control of axon shaft zippering
topic Biophysics and Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478281/
https://www.ncbi.nlm.nih.gov/pubmed/28422009
http://dx.doi.org/10.7554/eLife.19907
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