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Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C

The corpus callosum (CC) is the main pathway responsible for interhemispheric communication. CC agenesis is associated with numerous human pathologies, suggesting that a range of developmental defects can result in abnormalities in this structure. Midline glial cells are known to play a role in CC d...

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Autores principales: Niquille, Mathieu, Garel, Sonia, Mann, Fanny, Hornung, Jean-Pierre, Otsmane, Belkacem, Chevalley, Sébastien, Parras, Carlos, Guillemot, Francois, Gaspar, Patricia, Yanagawa, Yuchio, Lebrand, Cécile
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762166/
https://www.ncbi.nlm.nih.gov/pubmed/19859539
http://dx.doi.org/10.1371/journal.pbio.1000230
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author Niquille, Mathieu
Garel, Sonia
Mann, Fanny
Hornung, Jean-Pierre
Otsmane, Belkacem
Chevalley, Sébastien
Parras, Carlos
Guillemot, Francois
Gaspar, Patricia
Yanagawa, Yuchio
Lebrand, Cécile
author_facet Niquille, Mathieu
Garel, Sonia
Mann, Fanny
Hornung, Jean-Pierre
Otsmane, Belkacem
Chevalley, Sébastien
Parras, Carlos
Guillemot, Francois
Gaspar, Patricia
Yanagawa, Yuchio
Lebrand, Cécile
author_sort Niquille, Mathieu
collection PubMed
description The corpus callosum (CC) is the main pathway responsible for interhemispheric communication. CC agenesis is associated with numerous human pathologies, suggesting that a range of developmental defects can result in abnormalities in this structure. Midline glial cells are known to play a role in CC development, but we here show that two transient populations of midline neurons also make major contributions to the formation of this commissure. We report that these two neuronal populations enter the CC midline prior to the arrival of callosal pioneer axons. Using a combination of mutant analysis and in vitro assays, we demonstrate that CC neurons are necessary for normal callosal axon navigation. They exert an attractive influence on callosal axons, in part via Semaphorin 3C and its receptor Neuropilin-1. By revealing a novel and essential role for these neuronal populations in the pathfinding of a major cerebral commissure, our study brings new perspectives to pathophysiological mechanisms altering CC formation.
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spelling pubmed-27621662009-10-27 Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C Niquille, Mathieu Garel, Sonia Mann, Fanny Hornung, Jean-Pierre Otsmane, Belkacem Chevalley, Sébastien Parras, Carlos Guillemot, Francois Gaspar, Patricia Yanagawa, Yuchio Lebrand, Cécile PLoS Biol Research Article The corpus callosum (CC) is the main pathway responsible for interhemispheric communication. CC agenesis is associated with numerous human pathologies, suggesting that a range of developmental defects can result in abnormalities in this structure. Midline glial cells are known to play a role in CC development, but we here show that two transient populations of midline neurons also make major contributions to the formation of this commissure. We report that these two neuronal populations enter the CC midline prior to the arrival of callosal pioneer axons. Using a combination of mutant analysis and in vitro assays, we demonstrate that CC neurons are necessary for normal callosal axon navigation. They exert an attractive influence on callosal axons, in part via Semaphorin 3C and its receptor Neuropilin-1. By revealing a novel and essential role for these neuronal populations in the pathfinding of a major cerebral commissure, our study brings new perspectives to pathophysiological mechanisms altering CC formation. Public Library of Science 2009-10-27 /pmc/articles/PMC2762166/ /pubmed/19859539 http://dx.doi.org/10.1371/journal.pbio.1000230 Text en Niquille et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Niquille, Mathieu
Garel, Sonia
Mann, Fanny
Hornung, Jean-Pierre
Otsmane, Belkacem
Chevalley, Sébastien
Parras, Carlos
Guillemot, Francois
Gaspar, Patricia
Yanagawa, Yuchio
Lebrand, Cécile
Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C
title Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C
title_full Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C
title_fullStr Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C
title_full_unstemmed Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C
title_short Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C
title_sort transient neuronal populations are required to guide callosal axons: a role for semaphorin 3c
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762166/
https://www.ncbi.nlm.nih.gov/pubmed/19859539
http://dx.doi.org/10.1371/journal.pbio.1000230
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