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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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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 |
format | Online Article Text |
id | pubmed-5478281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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