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Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration

The developing nervous system is a complex yet organized system of neurons, glial support cells, and extracellular matrix that arranges into an elegant, highly structured network. The extracellular and intracellular events that guide axons to their target locations have been well characterized in ma...

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Autores principales: Rigby, Michael J., Gomez, Timothy M., Puglielli, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076157/
https://www.ncbi.nlm.nih.gov/pubmed/32210757
http://dx.doi.org/10.3389/fnins.2020.00203
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author Rigby, Michael J.
Gomez, Timothy M.
Puglielli, Luigi
author_facet Rigby, Michael J.
Gomez, Timothy M.
Puglielli, Luigi
author_sort Rigby, Michael J.
collection PubMed
description The developing nervous system is a complex yet organized system of neurons, glial support cells, and extracellular matrix that arranges into an elegant, highly structured network. The extracellular and intracellular events that guide axons to their target locations have been well characterized in many regions of the developing nervous system. However, despite extensive work, we have a poor understanding of how axonal growth cones interact with surrounding glial cells to regulate network assembly. Glia-to-growth cone communication is either direct through cellular contacts or indirect through modulation of the local microenvironment via the secretion of factors or signaling molecules. Microglia, oligodendrocytes, astrocytes, Schwann cells, neural progenitor cells, and olfactory ensheathing cells have all been demonstrated to directly impact axon growth and guidance. Expanding our understanding of how different glial cell types directly interact with growing axons throughout neurodevelopment will inform basic and clinical neuroscientists. For example, identifying the key cellular players beyond the axonal growth cone itself may provide translational clues to develop therapeutic interventions to modulate neuron growth during development or regeneration following injury. This review will provide an overview of the current knowledge about glial involvement in development of the nervous system, specifically focusing on how glia directly interact with growing and maturing axons to influence neuronal connectivity. This focus will be applied to the clinically-relevant field of regeneration following spinal cord injury, highlighting how a better understanding of the roles of glia in neurodevelopment can inform strategies to improve axon regeneration after injury.
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spelling pubmed-70761572020-03-24 Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration Rigby, Michael J. Gomez, Timothy M. Puglielli, Luigi Front Neurosci Neuroscience The developing nervous system is a complex yet organized system of neurons, glial support cells, and extracellular matrix that arranges into an elegant, highly structured network. The extracellular and intracellular events that guide axons to their target locations have been well characterized in many regions of the developing nervous system. However, despite extensive work, we have a poor understanding of how axonal growth cones interact with surrounding glial cells to regulate network assembly. Glia-to-growth cone communication is either direct through cellular contacts or indirect through modulation of the local microenvironment via the secretion of factors or signaling molecules. Microglia, oligodendrocytes, astrocytes, Schwann cells, neural progenitor cells, and olfactory ensheathing cells have all been demonstrated to directly impact axon growth and guidance. Expanding our understanding of how different glial cell types directly interact with growing axons throughout neurodevelopment will inform basic and clinical neuroscientists. For example, identifying the key cellular players beyond the axonal growth cone itself may provide translational clues to develop therapeutic interventions to modulate neuron growth during development or regeneration following injury. This review will provide an overview of the current knowledge about glial involvement in development of the nervous system, specifically focusing on how glia directly interact with growing and maturing axons to influence neuronal connectivity. This focus will be applied to the clinically-relevant field of regeneration following spinal cord injury, highlighting how a better understanding of the roles of glia in neurodevelopment can inform strategies to improve axon regeneration after injury. Frontiers Media S.A. 2020-03-10 /pmc/articles/PMC7076157/ /pubmed/32210757 http://dx.doi.org/10.3389/fnins.2020.00203 Text en Copyright © 2020 Rigby, Gomez and Puglielli. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Rigby, Michael J.
Gomez, Timothy M.
Puglielli, Luigi
Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration
title Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration
title_full Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration
title_fullStr Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration
title_full_unstemmed Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration
title_short Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration
title_sort glial cell-axonal growth cone interactions in neurodevelopment and regeneration
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076157/
https://www.ncbi.nlm.nih.gov/pubmed/32210757
http://dx.doi.org/10.3389/fnins.2020.00203
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