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A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion
Axons navigate long distances through complex 3D environments to interconnect the nervous system during development. Although the precise spatiotemporal effects of most axon guidance cues remain poorly characterized, a prevailing model posits that attractive guidance cues stimulate actin polymerizat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084274/ https://www.ncbi.nlm.nih.gov/pubmed/27091449 http://dx.doi.org/10.1083/jcb.201509062 |
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author | McConnell, Russell E. Edward van Veen, J. Vidaki, Marina Kwiatkowski, Adam V. Meyer, Aaron S. Gertler, Frank B. |
author_facet | McConnell, Russell E. Edward van Veen, J. Vidaki, Marina Kwiatkowski, Adam V. Meyer, Aaron S. Gertler, Frank B. |
author_sort | McConnell, Russell E. |
collection | PubMed |
description | Axons navigate long distances through complex 3D environments to interconnect the nervous system during development. Although the precise spatiotemporal effects of most axon guidance cues remain poorly characterized, a prevailing model posits that attractive guidance cues stimulate actin polymerization in neuronal growth cones whereas repulsive cues induce actin disassembly. Contrary to this model, we find that the repulsive guidance cue Slit stimulates the formation and elongation of actin-based filopodia from mouse dorsal root ganglion growth cones. Surprisingly, filopodia form and elongate toward sources of Slit, a response that we find is required for subsequent axonal repulsion away from Slit. Mechanistically, Slit evokes changes in filopodium dynamics by increasing direct binding of its receptor, Robo, to members of the actin-regulatory Ena/VASP family. Perturbing filopodium dynamics pharmacologically or genetically disrupts Slit-mediated repulsion and produces severe axon guidance defects in vivo. Thus, Slit locally stimulates directional filopodial extension, a process that is required for subsequent axonal repulsion downstream of the Robo receptor. |
format | Online Article Text |
id | pubmed-5084274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50842742016-10-31 A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion McConnell, Russell E. Edward van Veen, J. Vidaki, Marina Kwiatkowski, Adam V. Meyer, Aaron S. Gertler, Frank B. J Cell Biol Research Articles Axons navigate long distances through complex 3D environments to interconnect the nervous system during development. Although the precise spatiotemporal effects of most axon guidance cues remain poorly characterized, a prevailing model posits that attractive guidance cues stimulate actin polymerization in neuronal growth cones whereas repulsive cues induce actin disassembly. Contrary to this model, we find that the repulsive guidance cue Slit stimulates the formation and elongation of actin-based filopodia from mouse dorsal root ganglion growth cones. Surprisingly, filopodia form and elongate toward sources of Slit, a response that we find is required for subsequent axonal repulsion away from Slit. Mechanistically, Slit evokes changes in filopodium dynamics by increasing direct binding of its receptor, Robo, to members of the actin-regulatory Ena/VASP family. Perturbing filopodium dynamics pharmacologically or genetically disrupts Slit-mediated repulsion and produces severe axon guidance defects in vivo. Thus, Slit locally stimulates directional filopodial extension, a process that is required for subsequent axonal repulsion downstream of the Robo receptor. The Rockefeller University Press 2016-04-25 /pmc/articles/PMC5084274/ /pubmed/27091449 http://dx.doi.org/10.1083/jcb.201509062 Text en © 2016 McConnell et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles McConnell, Russell E. Edward van Veen, J. Vidaki, Marina Kwiatkowski, Adam V. Meyer, Aaron S. Gertler, Frank B. A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion |
title | A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion |
title_full | A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion |
title_fullStr | A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion |
title_full_unstemmed | A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion |
title_short | A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion |
title_sort | requirement for filopodia extension toward slit during robo-mediated axon repulsion |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084274/ https://www.ncbi.nlm.nih.gov/pubmed/27091449 http://dx.doi.org/10.1083/jcb.201509062 |
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