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Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain

Mature mammalian brains consist of variety of neuronal and non-neuronal cell types, which are progressively generated from embryonic neural progenitors through the embryonic and postnatal periods. However, it remains unknown whether all embryonic progenitors equivalently contribute to multiple cell...

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Autores principales: Hashimoto, Yuki, Gotoh, Hitoshi, Ono, Katsuhiko, Nomura, Tadashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418204/
https://www.ncbi.nlm.nih.gov/pubmed/30872629
http://dx.doi.org/10.1038/s41598-019-40599-2
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author Hashimoto, Yuki
Gotoh, Hitoshi
Ono, Katsuhiko
Nomura, Tadashi
author_facet Hashimoto, Yuki
Gotoh, Hitoshi
Ono, Katsuhiko
Nomura, Tadashi
author_sort Hashimoto, Yuki
collection PubMed
description Mature mammalian brains consist of variety of neuronal and non-neuronal cell types, which are progressively generated from embryonic neural progenitors through the embryonic and postnatal periods. However, it remains unknown whether all embryonic progenitors equivalently contribute to multiple cell types, or individual neural progenitors have variable potentials to generate specific cell types in a stochastic manner. Here, we performed population-level tracing of mouse embryonic neural progenitors by using Tol2-mediated genome integration vectors. We identified that neural progenitors in early embryonic stages predominantly contribute to cortical or subcortical neurons than astrocytes, ependymal cells, and neuroblasts in the postnatal brain. Notably, neurons and astrocytes were cumulatively labeled by the increase of total labeled cells, suggesting constant neurogenic and gliogenic potentials of individual neural progenitors. On the contrary, numbers of labeled ependymal cell are more fluctuated, implicating intrinsic variability of progenitor potentials for ependymal cell generation. Differential progenitor potentials that contribute to neurons, astrocytes, and ependymal cells were also detected in the developing avian pallium. Our data suggest evolutionary conservations of coherent and variable potentials of neural progenitors that generate multiple cell types in the developing amniote brain.
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spelling pubmed-64182042019-03-18 Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain Hashimoto, Yuki Gotoh, Hitoshi Ono, Katsuhiko Nomura, Tadashi Sci Rep Article Mature mammalian brains consist of variety of neuronal and non-neuronal cell types, which are progressively generated from embryonic neural progenitors through the embryonic and postnatal periods. However, it remains unknown whether all embryonic progenitors equivalently contribute to multiple cell types, or individual neural progenitors have variable potentials to generate specific cell types in a stochastic manner. Here, we performed population-level tracing of mouse embryonic neural progenitors by using Tol2-mediated genome integration vectors. We identified that neural progenitors in early embryonic stages predominantly contribute to cortical or subcortical neurons than astrocytes, ependymal cells, and neuroblasts in the postnatal brain. Notably, neurons and astrocytes were cumulatively labeled by the increase of total labeled cells, suggesting constant neurogenic and gliogenic potentials of individual neural progenitors. On the contrary, numbers of labeled ependymal cell are more fluctuated, implicating intrinsic variability of progenitor potentials for ependymal cell generation. Differential progenitor potentials that contribute to neurons, astrocytes, and ependymal cells were also detected in the developing avian pallium. Our data suggest evolutionary conservations of coherent and variable potentials of neural progenitors that generate multiple cell types in the developing amniote brain. Nature Publishing Group UK 2019-03-14 /pmc/articles/PMC6418204/ /pubmed/30872629 http://dx.doi.org/10.1038/s41598-019-40599-2 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hashimoto, Yuki
Gotoh, Hitoshi
Ono, Katsuhiko
Nomura, Tadashi
Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain
title Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain
title_full Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain
title_fullStr Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain
title_full_unstemmed Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain
title_short Differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain
title_sort differential potentials of neural progenitors for the generation of neurons and non-neuronal cells in the developing amniote brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418204/
https://www.ncbi.nlm.nih.gov/pubmed/30872629
http://dx.doi.org/10.1038/s41598-019-40599-2
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