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Lineage hierarchies and stochasticity ensure the long-term maintenance of adult neural stem cells
The cellular basis and extent of neural stem cell (NSC) self-renewal in adult vertebrates, and their heterogeneity, remain controversial. To explore the functional behavior and dynamics of individual NSCs, we combined genetic lineage tracing, quantitative clonal analysis, intravital imaging, and glo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190328/ https://www.ncbi.nlm.nih.gov/pubmed/32426477 http://dx.doi.org/10.1126/sciadv.aaz5424 |
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author | Than-Trong, Emmanuel Kiani, Bahareh Dray, Nicolas Ortica, Sara Simons, Benjamin Rulands, Steffen Alunni, Alessandro Bally-Cuif, Laure |
author_facet | Than-Trong, Emmanuel Kiani, Bahareh Dray, Nicolas Ortica, Sara Simons, Benjamin Rulands, Steffen Alunni, Alessandro Bally-Cuif, Laure |
author_sort | Than-Trong, Emmanuel |
collection | PubMed |
description | The cellular basis and extent of neural stem cell (NSC) self-renewal in adult vertebrates, and their heterogeneity, remain controversial. To explore the functional behavior and dynamics of individual NSCs, we combined genetic lineage tracing, quantitative clonal analysis, intravital imaging, and global population assessments in the adult zebrafish telencephalon. Our results are compatible with a model where adult neurogenesis is organized in a hierarchy in which a subpopulation of deeply quiescent reservoir NSCs with long-term self-renewal potential generate, through asymmetric divisions, a pool of operational NSCs activating more frequently and taking stochastic fates biased toward neuronal differentiation. Our data further suggest the existence of an additional, upstream, progenitor population that supports the continuous generation of new reservoir NSCs, thus contributing to their overall expansion. Hence, we propose that the dynamics of vertebrate neurogenesis relies on a hierarchical organization where growth, self-renewal, and neurogenic functions are segregated between different NSC types. |
format | Online Article Text |
id | pubmed-7190328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71903282020-05-18 Lineage hierarchies and stochasticity ensure the long-term maintenance of adult neural stem cells Than-Trong, Emmanuel Kiani, Bahareh Dray, Nicolas Ortica, Sara Simons, Benjamin Rulands, Steffen Alunni, Alessandro Bally-Cuif, Laure Sci Adv Research Articles The cellular basis and extent of neural stem cell (NSC) self-renewal in adult vertebrates, and their heterogeneity, remain controversial. To explore the functional behavior and dynamics of individual NSCs, we combined genetic lineage tracing, quantitative clonal analysis, intravital imaging, and global population assessments in the adult zebrafish telencephalon. Our results are compatible with a model where adult neurogenesis is organized in a hierarchy in which a subpopulation of deeply quiescent reservoir NSCs with long-term self-renewal potential generate, through asymmetric divisions, a pool of operational NSCs activating more frequently and taking stochastic fates biased toward neuronal differentiation. Our data further suggest the existence of an additional, upstream, progenitor population that supports the continuous generation of new reservoir NSCs, thus contributing to their overall expansion. Hence, we propose that the dynamics of vertebrate neurogenesis relies on a hierarchical organization where growth, self-renewal, and neurogenic functions are segregated between different NSC types. American Association for the Advancement of Science 2020-04-29 /pmc/articles/PMC7190328/ /pubmed/32426477 http://dx.doi.org/10.1126/sciadv.aaz5424 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Than-Trong, Emmanuel Kiani, Bahareh Dray, Nicolas Ortica, Sara Simons, Benjamin Rulands, Steffen Alunni, Alessandro Bally-Cuif, Laure Lineage hierarchies and stochasticity ensure the long-term maintenance of adult neural stem cells |
title | Lineage hierarchies and stochasticity ensure the long-term maintenance of adult neural stem cells |
title_full | Lineage hierarchies and stochasticity ensure the long-term maintenance of adult neural stem cells |
title_fullStr | Lineage hierarchies and stochasticity ensure the long-term maintenance of adult neural stem cells |
title_full_unstemmed | Lineage hierarchies and stochasticity ensure the long-term maintenance of adult neural stem cells |
title_short | Lineage hierarchies and stochasticity ensure the long-term maintenance of adult neural stem cells |
title_sort | lineage hierarchies and stochasticity ensure the long-term maintenance of adult neural stem cells |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190328/ https://www.ncbi.nlm.nih.gov/pubmed/32426477 http://dx.doi.org/10.1126/sciadv.aaz5424 |
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