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Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development

Glutamatergic neurons of the mammalian cerebral cortex originate from radial glia (RG) progenitors in the ventricular zone (VZ). During corticogenesis, neuroblasts migrate toward the pial surface using two different migration modes. One is multipolar (MP) migration with random directional movement,...

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Autores principales: Ohtaka-Maruyama, Chiaki, Okado, Haruo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682034/
https://www.ncbi.nlm.nih.gov/pubmed/26733777
http://dx.doi.org/10.3389/fnins.2015.00447
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author Ohtaka-Maruyama, Chiaki
Okado, Haruo
author_facet Ohtaka-Maruyama, Chiaki
Okado, Haruo
author_sort Ohtaka-Maruyama, Chiaki
collection PubMed
description Glutamatergic neurons of the mammalian cerebral cortex originate from radial glia (RG) progenitors in the ventricular zone (VZ). During corticogenesis, neuroblasts migrate toward the pial surface using two different migration modes. One is multipolar (MP) migration with random directional movement, and the other is locomotion, which is a unidirectional movement guided by the RG fiber. After reaching their final destination, the neurons finalize their migration by terminal translocation, which is followed by maturation via dendrite extension to initiate synaptogenesis and thereby complete neural circuit formation. This switching of migration modes during cortical development is unique in mammals, which suggests that the RG-guided locomotion mode may contribute to the evolution of the mammalian neocortical 6-layer structure. Many factors have been reported to be involved in the regulation of this radial neuronal migration process. In general, the radial migration can be largely divided into four steps; (1) maintenance and departure from the VZ of neural progenitor cells, (2) MP migration and transition to bipolar cells, (3) RG-guided locomotion, and (4) terminal translocation and dendrite maturation. Among these, many different gene mutations or knockdown effects have resulted in failure of the MP to bipolar transition (step 2), suggesting that it is a critical step, particularly in radial migration. Moreover, this transition occurs at the subplate layer. In this review, we summarize recent advances in our understanding of the molecular mechanisms underlying each of these steps. Finally, we discuss the evolutionary aspects of neuronal migration in corticogenesis.
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spelling pubmed-46820342016-01-05 Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development Ohtaka-Maruyama, Chiaki Okado, Haruo Front Neurosci Neuroscience Glutamatergic neurons of the mammalian cerebral cortex originate from radial glia (RG) progenitors in the ventricular zone (VZ). During corticogenesis, neuroblasts migrate toward the pial surface using two different migration modes. One is multipolar (MP) migration with random directional movement, and the other is locomotion, which is a unidirectional movement guided by the RG fiber. After reaching their final destination, the neurons finalize their migration by terminal translocation, which is followed by maturation via dendrite extension to initiate synaptogenesis and thereby complete neural circuit formation. This switching of migration modes during cortical development is unique in mammals, which suggests that the RG-guided locomotion mode may contribute to the evolution of the mammalian neocortical 6-layer structure. Many factors have been reported to be involved in the regulation of this radial neuronal migration process. In general, the radial migration can be largely divided into four steps; (1) maintenance and departure from the VZ of neural progenitor cells, (2) MP migration and transition to bipolar cells, (3) RG-guided locomotion, and (4) terminal translocation and dendrite maturation. Among these, many different gene mutations or knockdown effects have resulted in failure of the MP to bipolar transition (step 2), suggesting that it is a critical step, particularly in radial migration. Moreover, this transition occurs at the subplate layer. In this review, we summarize recent advances in our understanding of the molecular mechanisms underlying each of these steps. Finally, we discuss the evolutionary aspects of neuronal migration in corticogenesis. Frontiers Media S.A. 2015-12-17 /pmc/articles/PMC4682034/ /pubmed/26733777 http://dx.doi.org/10.3389/fnins.2015.00447 Text en Copyright © 2015 Ohtaka-Maruyama and Okado. 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) or licensor 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
Ohtaka-Maruyama, Chiaki
Okado, Haruo
Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development
title Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development
title_full Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development
title_fullStr Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development
title_full_unstemmed Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development
title_short Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development
title_sort molecular pathways underlying projection neuron production and migration during cerebral cortical development
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682034/
https://www.ncbi.nlm.nih.gov/pubmed/26733777
http://dx.doi.org/10.3389/fnins.2015.00447
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