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Mechanical tension can specify axonal fate in hippocampal neurons

Here we asked whether applied mechanical tension would stimulate undifferentiated minor processes of cultured hippocampal neurons to become axons and whether tension could induce a second axon in an already polarized neuron. Experimental tension applied to minor processes produced extensions that de...

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Detalles Bibliográficos
Autores principales: Lamoureux, Phillip, Ruthel, Gordon, Buxbaum, Robert E., Heidemann, Steven R.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173080/
https://www.ncbi.nlm.nih.gov/pubmed/12417580
http://dx.doi.org/10.1083/jcb.200207174
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author Lamoureux, Phillip
Ruthel, Gordon
Buxbaum, Robert E.
Heidemann, Steven R.
author_facet Lamoureux, Phillip
Ruthel, Gordon
Buxbaum, Robert E.
Heidemann, Steven R.
author_sort Lamoureux, Phillip
collection PubMed
description Here we asked whether applied mechanical tension would stimulate undifferentiated minor processes of cultured hippocampal neurons to become axons and whether tension could induce a second axon in an already polarized neuron. Experimental tension applied to minor processes produced extensions that demonstrated axonal character, regardless of the presence of an existing axon. Towed neurites showed a high rate of spontaneous growth cone advance and could continue to grow out for 1–3 d after towing. The developmental course of experimental neurites was found to be similar to that of unmanipulated spontaneous axons. Furthermore, the experimentally elongated neurites showed compartmentation of the axonal markers dephospho-tau and L-1 in towed outgrowth after 24 h. Extension of a second axon from an already polarized neuron does not lead to the loss of the spontaneous axon either immediately or after longer term growth. In addition, we were able to initiate neurites de novo that subsequently acquired axonal character even though spontaneous growth cone advance began while the towed neurite was still no longer than its sibling processes. This suggests that tension rather than the achievement of a critical neurite length determined axonal specification.
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spelling pubmed-21730802008-05-01 Mechanical tension can specify axonal fate in hippocampal neurons Lamoureux, Phillip Ruthel, Gordon Buxbaum, Robert E. Heidemann, Steven R. J Cell Biol Article Here we asked whether applied mechanical tension would stimulate undifferentiated minor processes of cultured hippocampal neurons to become axons and whether tension could induce a second axon in an already polarized neuron. Experimental tension applied to minor processes produced extensions that demonstrated axonal character, regardless of the presence of an existing axon. Towed neurites showed a high rate of spontaneous growth cone advance and could continue to grow out for 1–3 d after towing. The developmental course of experimental neurites was found to be similar to that of unmanipulated spontaneous axons. Furthermore, the experimentally elongated neurites showed compartmentation of the axonal markers dephospho-tau and L-1 in towed outgrowth after 24 h. Extension of a second axon from an already polarized neuron does not lead to the loss of the spontaneous axon either immediately or after longer term growth. In addition, we were able to initiate neurites de novo that subsequently acquired axonal character even though spontaneous growth cone advance began while the towed neurite was still no longer than its sibling processes. This suggests that tension rather than the achievement of a critical neurite length determined axonal specification. The Rockefeller University Press 2002-11-11 /pmc/articles/PMC2173080/ /pubmed/12417580 http://dx.doi.org/10.1083/jcb.200207174 Text en Copyright © 2002, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Lamoureux, Phillip
Ruthel, Gordon
Buxbaum, Robert E.
Heidemann, Steven R.
Mechanical tension can specify axonal fate in hippocampal neurons
title Mechanical tension can specify axonal fate in hippocampal neurons
title_full Mechanical tension can specify axonal fate in hippocampal neurons
title_fullStr Mechanical tension can specify axonal fate in hippocampal neurons
title_full_unstemmed Mechanical tension can specify axonal fate in hippocampal neurons
title_short Mechanical tension can specify axonal fate in hippocampal neurons
title_sort mechanical tension can specify axonal fate in hippocampal neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173080/
https://www.ncbi.nlm.nih.gov/pubmed/12417580
http://dx.doi.org/10.1083/jcb.200207174
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