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Mechanosensing is critical for axon growth in the developing brain

During nervous system development, neurons extend axons along well-defined pathways. The current understanding of axon pathfinding is based mainly on chemical signalling. However, growing neurons interact not only chemically but also mechanically with their environment. Here we identify mechanical s...

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Autores principales: Koser, David E., Thompson, Amelia J., Foster, Sarah K., Dwivedy, Asha, Pillai, Eva K., Sheridan, Graham K., Svoboda, Hanno, Viana, Matheus, da F. Costa, Luciano, Guck, Jochen, Holt, Christine E., Franze, Kristian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531257/
https://www.ncbi.nlm.nih.gov/pubmed/27643431
http://dx.doi.org/10.1038/nn.4394
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author Koser, David E.
Thompson, Amelia J.
Foster, Sarah K.
Dwivedy, Asha
Pillai, Eva K.
Sheridan, Graham K.
Svoboda, Hanno
Viana, Matheus
da F. Costa, Luciano
Guck, Jochen
Holt, Christine E.
Franze, Kristian
author_facet Koser, David E.
Thompson, Amelia J.
Foster, Sarah K.
Dwivedy, Asha
Pillai, Eva K.
Sheridan, Graham K.
Svoboda, Hanno
Viana, Matheus
da F. Costa, Luciano
Guck, Jochen
Holt, Christine E.
Franze, Kristian
author_sort Koser, David E.
collection PubMed
description During nervous system development, neurons extend axons along well-defined pathways. The current understanding of axon pathfinding is based mainly on chemical signalling. However, growing neurons interact not only chemically but also mechanically with their environment. Here we identify mechanical signals as important regulators of axon pathfinding. In vitro, substrate stiffness determined growth patterns of Xenopus retinal ganglion cell (RGC) axons. In vivo atomic force microscopy revealed striking stiffness gradient patterns in the embryonic brain. RGC axons grew towards the tissue’s softer side, which was reproduced in vitro in the absence of chemical gradients. To test the importance of mechanical signals for axon growth in vivo, we altered brain stiffness, blocked mechanotransduction pharmacologically, and knocked down the mechanosensitive ion channel Piezo1. All treatments resulted in aberrant axonal growth and pathfinding errors, suggesting that local tissue stiffness–read out by mechanosensitive ion channels–is critically involved in instructing neuronal growth in vivo.
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spelling pubmed-55312572017-07-27 Mechanosensing is critical for axon growth in the developing brain Koser, David E. Thompson, Amelia J. Foster, Sarah K. Dwivedy, Asha Pillai, Eva K. Sheridan, Graham K. Svoboda, Hanno Viana, Matheus da F. Costa, Luciano Guck, Jochen Holt, Christine E. Franze, Kristian Nat Neurosci Article During nervous system development, neurons extend axons along well-defined pathways. The current understanding of axon pathfinding is based mainly on chemical signalling. However, growing neurons interact not only chemically but also mechanically with their environment. Here we identify mechanical signals as important regulators of axon pathfinding. In vitro, substrate stiffness determined growth patterns of Xenopus retinal ganglion cell (RGC) axons. In vivo atomic force microscopy revealed striking stiffness gradient patterns in the embryonic brain. RGC axons grew towards the tissue’s softer side, which was reproduced in vitro in the absence of chemical gradients. To test the importance of mechanical signals for axon growth in vivo, we altered brain stiffness, blocked mechanotransduction pharmacologically, and knocked down the mechanosensitive ion channel Piezo1. All treatments resulted in aberrant axonal growth and pathfinding errors, suggesting that local tissue stiffness–read out by mechanosensitive ion channels–is critically involved in instructing neuronal growth in vivo. 2016-09-19 2016-12 /pmc/articles/PMC5531257/ /pubmed/27643431 http://dx.doi.org/10.1038/nn.4394 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Koser, David E.
Thompson, Amelia J.
Foster, Sarah K.
Dwivedy, Asha
Pillai, Eva K.
Sheridan, Graham K.
Svoboda, Hanno
Viana, Matheus
da F. Costa, Luciano
Guck, Jochen
Holt, Christine E.
Franze, Kristian
Mechanosensing is critical for axon growth in the developing brain
title Mechanosensing is critical for axon growth in the developing brain
title_full Mechanosensing is critical for axon growth in the developing brain
title_fullStr Mechanosensing is critical for axon growth in the developing brain
title_full_unstemmed Mechanosensing is critical for axon growth in the developing brain
title_short Mechanosensing is critical for axon growth in the developing brain
title_sort mechanosensing is critical for axon growth in the developing brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531257/
https://www.ncbi.nlm.nih.gov/pubmed/27643431
http://dx.doi.org/10.1038/nn.4394
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