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Extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit
To form functional neural circuits, neurons migrate to their final destination and extend axons towards their targets. Whether and how these two processes are coordinated in vivo remains elusive. We use the zebrafish olfactory placode as a system to address the underlying mechanisms. Quantitative li...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561127/ https://www.ncbi.nlm.nih.gov/pubmed/28819208 http://dx.doi.org/10.1038/s41467-017-00283-3 |
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author | Breau, M. A. Bonnet, I. Stoufflet, J. Xie, J. De Castro, S. Schneider-Maunoury, S. |
author_facet | Breau, M. A. Bonnet, I. Stoufflet, J. Xie, J. De Castro, S. Schneider-Maunoury, S. |
author_sort | Breau, M. A. |
collection | PubMed |
description | To form functional neural circuits, neurons migrate to their final destination and extend axons towards their targets. Whether and how these two processes are coordinated in vivo remains elusive. We use the zebrafish olfactory placode as a system to address the underlying mechanisms. Quantitative live imaging uncovers a choreography of directed cell movements that shapes the placode neuronal cluster: convergence of cells towards the centre of the placodal domain and lateral cell movements away from the brain. Axon formation is concomitant with lateral movements and occurs through an unexpected, retrograde mode of extension, where cell bodies move away from axon tips attached to the brain surface. Convergence movements are active, whereas cell body lateral displacements are of mainly passive nature, likely triggered by compression forces from converging neighbouring cells. These findings unravel a previously unknown mechanism of neuronal circuit formation, whereby extrinsic mechanical forces drive the retrograde extension of axons. |
format | Online Article Text |
id | pubmed-5561127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55611272017-08-28 Extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit Breau, M. A. Bonnet, I. Stoufflet, J. Xie, J. De Castro, S. Schneider-Maunoury, S. Nat Commun Article To form functional neural circuits, neurons migrate to their final destination and extend axons towards their targets. Whether and how these two processes are coordinated in vivo remains elusive. We use the zebrafish olfactory placode as a system to address the underlying mechanisms. Quantitative live imaging uncovers a choreography of directed cell movements that shapes the placode neuronal cluster: convergence of cells towards the centre of the placodal domain and lateral cell movements away from the brain. Axon formation is concomitant with lateral movements and occurs through an unexpected, retrograde mode of extension, where cell bodies move away from axon tips attached to the brain surface. Convergence movements are active, whereas cell body lateral displacements are of mainly passive nature, likely triggered by compression forces from converging neighbouring cells. These findings unravel a previously unknown mechanism of neuronal circuit formation, whereby extrinsic mechanical forces drive the retrograde extension of axons. Nature Publishing Group UK 2017-08-17 /pmc/articles/PMC5561127/ /pubmed/28819208 http://dx.doi.org/10.1038/s41467-017-00283-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Breau, M. A. Bonnet, I. Stoufflet, J. Xie, J. De Castro, S. Schneider-Maunoury, S. Extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit |
title | Extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit |
title_full | Extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit |
title_fullStr | Extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit |
title_full_unstemmed | Extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit |
title_short | Extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit |
title_sort | extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561127/ https://www.ncbi.nlm.nih.gov/pubmed/28819208 http://dx.doi.org/10.1038/s41467-017-00283-3 |
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