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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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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. |
format | Online Article Text |
id | pubmed-5531257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
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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