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Basal Protrusions Mediate Spatiotemporal Patterns of Spinal Neuron Differentiation
During early spinal cord development, neurons of particular subtypes differentiate with a sparse periodic pattern while later neurons differentiate in the intervening space to eventually produce continuous columns of similar neurons. The mechanisms that regulate this spatiotemporal pattern are unkno...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584357/ https://www.ncbi.nlm.nih.gov/pubmed/31211994 http://dx.doi.org/10.1016/j.devcel.2019.05.035 |
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author | Hadjivasiliou, Zena Moore, Rachel E. McIntosh, Rebecca Galea, Gabriel L. Clarke, Jonathan D.W. Alexandre, Paula |
author_facet | Hadjivasiliou, Zena Moore, Rachel E. McIntosh, Rebecca Galea, Gabriel L. Clarke, Jonathan D.W. Alexandre, Paula |
author_sort | Hadjivasiliou, Zena |
collection | PubMed |
description | During early spinal cord development, neurons of particular subtypes differentiate with a sparse periodic pattern while later neurons differentiate in the intervening space to eventually produce continuous columns of similar neurons. The mechanisms that regulate this spatiotemporal pattern are unknown. In vivo imaging in zebrafish reveals that differentiating spinal neurons transiently extend two long protrusions along the basal surface of the spinal cord before axon initiation. These protrusions express Delta protein, consistent with the hypothesis they influence Notch signaling at a distance of several cell diameters. Experimental reduction of Laminin expression leads to smaller protrusions and shorter distances between differentiating neurons. The experimental data and a theoretical model support the proposal that neuronal differentiation pattern is regulated by transient basal protrusions that deliver temporally controlled lateral inhibition mediated at a distance. This work uncovers a stereotyped protrusive activity of newborn neurons that organize long-distance spatiotemporal patterning of differentiation. |
format | Online Article Text |
id | pubmed-6584357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-65843572019-06-27 Basal Protrusions Mediate Spatiotemporal Patterns of Spinal Neuron Differentiation Hadjivasiliou, Zena Moore, Rachel E. McIntosh, Rebecca Galea, Gabriel L. Clarke, Jonathan D.W. Alexandre, Paula Dev Cell Article During early spinal cord development, neurons of particular subtypes differentiate with a sparse periodic pattern while later neurons differentiate in the intervening space to eventually produce continuous columns of similar neurons. The mechanisms that regulate this spatiotemporal pattern are unknown. In vivo imaging in zebrafish reveals that differentiating spinal neurons transiently extend two long protrusions along the basal surface of the spinal cord before axon initiation. These protrusions express Delta protein, consistent with the hypothesis they influence Notch signaling at a distance of several cell diameters. Experimental reduction of Laminin expression leads to smaller protrusions and shorter distances between differentiating neurons. The experimental data and a theoretical model support the proposal that neuronal differentiation pattern is regulated by transient basal protrusions that deliver temporally controlled lateral inhibition mediated at a distance. This work uncovers a stereotyped protrusive activity of newborn neurons that organize long-distance spatiotemporal patterning of differentiation. Cell Press 2019-06-17 /pmc/articles/PMC6584357/ /pubmed/31211994 http://dx.doi.org/10.1016/j.devcel.2019.05.035 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hadjivasiliou, Zena Moore, Rachel E. McIntosh, Rebecca Galea, Gabriel L. Clarke, Jonathan D.W. Alexandre, Paula Basal Protrusions Mediate Spatiotemporal Patterns of Spinal Neuron Differentiation |
title | Basal Protrusions Mediate Spatiotemporal Patterns of Spinal Neuron Differentiation |
title_full | Basal Protrusions Mediate Spatiotemporal Patterns of Spinal Neuron Differentiation |
title_fullStr | Basal Protrusions Mediate Spatiotemporal Patterns of Spinal Neuron Differentiation |
title_full_unstemmed | Basal Protrusions Mediate Spatiotemporal Patterns of Spinal Neuron Differentiation |
title_short | Basal Protrusions Mediate Spatiotemporal Patterns of Spinal Neuron Differentiation |
title_sort | basal protrusions mediate spatiotemporal patterns of spinal neuron differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584357/ https://www.ncbi.nlm.nih.gov/pubmed/31211994 http://dx.doi.org/10.1016/j.devcel.2019.05.035 |
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