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Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation

Guidepost cells present at and surrounding the midline provide guidance cues that orient the growing axons through commissures. Here we show that the transcription factor Nkx2.1 known to control the specification of GABAergic interneurons also regulates the differentiation of astroglia and polydendr...

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Autores principales: Minocha, Shilpi, Valloton, Delphine, Ypsilanti, Athena R., Fiumelli, Hubert, Allen, Elizabeth A., Yanagawa, Yuchio, Marin, Oscar, Chédotal, Alain, Hornung, Jean-Pierre, Lebrand, Cécile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423212/
https://www.ncbi.nlm.nih.gov/pubmed/25904499
http://dx.doi.org/10.1038/ncomms7887
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author Minocha, Shilpi
Valloton, Delphine
Ypsilanti, Athena R.
Fiumelli, Hubert
Allen, Elizabeth A.
Yanagawa, Yuchio
Marin, Oscar
Chédotal, Alain
Hornung, Jean-Pierre
Lebrand, Cécile
author_facet Minocha, Shilpi
Valloton, Delphine
Ypsilanti, Athena R.
Fiumelli, Hubert
Allen, Elizabeth A.
Yanagawa, Yuchio
Marin, Oscar
Chédotal, Alain
Hornung, Jean-Pierre
Lebrand, Cécile
author_sort Minocha, Shilpi
collection PubMed
description Guidepost cells present at and surrounding the midline provide guidance cues that orient the growing axons through commissures. Here we show that the transcription factor Nkx2.1 known to control the specification of GABAergic interneurons also regulates the differentiation of astroglia and polydendrocytes within the mouse anterior commissure (AC). Nkx2.1-positive glia were found to originate from three germinal regions of the ventral telencephalon. Nkx2.1-derived glia were observed in and around the AC region by E14.5. Thereafter, a selective cell ablation strategy showed a synergistic role of Nkx2.1-derived cells, both GABAergic interneurons and astroglia, towards the proper formation of the AC. Finally, our results reveal that the Nkx2.1-regulated cells mediate AC axon guidance through the expression of the repellent cue, Slit2. These results bring forth interesting insights about the spatial and temporal origin of midline telencephalic glia, and highlight the importance of neurons and astroglia towards the formation of midline commissures.
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spelling pubmed-44232122015-05-20 Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation Minocha, Shilpi Valloton, Delphine Ypsilanti, Athena R. Fiumelli, Hubert Allen, Elizabeth A. Yanagawa, Yuchio Marin, Oscar Chédotal, Alain Hornung, Jean-Pierre Lebrand, Cécile Nat Commun Article Guidepost cells present at and surrounding the midline provide guidance cues that orient the growing axons through commissures. Here we show that the transcription factor Nkx2.1 known to control the specification of GABAergic interneurons also regulates the differentiation of astroglia and polydendrocytes within the mouse anterior commissure (AC). Nkx2.1-positive glia were found to originate from three germinal regions of the ventral telencephalon. Nkx2.1-derived glia were observed in and around the AC region by E14.5. Thereafter, a selective cell ablation strategy showed a synergistic role of Nkx2.1-derived cells, both GABAergic interneurons and astroglia, towards the proper formation of the AC. Finally, our results reveal that the Nkx2.1-regulated cells mediate AC axon guidance through the expression of the repellent cue, Slit2. These results bring forth interesting insights about the spatial and temporal origin of midline telencephalic glia, and highlight the importance of neurons and astroglia towards the formation of midline commissures. Nature Pub. Group 2015-04-23 /pmc/articles/PMC4423212/ /pubmed/25904499 http://dx.doi.org/10.1038/ncomms7887 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Minocha, Shilpi
Valloton, Delphine
Ypsilanti, Athena R.
Fiumelli, Hubert
Allen, Elizabeth A.
Yanagawa, Yuchio
Marin, Oscar
Chédotal, Alain
Hornung, Jean-Pierre
Lebrand, Cécile
Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation
title Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation
title_full Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation
title_fullStr Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation
title_full_unstemmed Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation
title_short Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation
title_sort nkx2.1-derived astrocytes and neurons together with slit2 are indispensable for anterior commissure formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423212/
https://www.ncbi.nlm.nih.gov/pubmed/25904499
http://dx.doi.org/10.1038/ncomms7887
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