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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...

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Autores principales: Hadjivasiliou, Zena, Moore, Rachel E., McIntosh, Rebecca, Galea, Gabriel L., Clarke, Jonathan D.W., Alexandre, Paula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
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.
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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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