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Conserved and Divergent Features of Adult Neurogenesis in Zebrafish
Adult neurogenesis, i.e., the generation of neurons from neural stem cells (NSCs) in the adult brain, contributes to brain plasticity in all vertebrates. It varies, however, greatly in extent, location and physiological characteristics between species. During the last decade, the teleost zebrafish (...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338623/ https://www.ncbi.nlm.nih.gov/pubmed/32695781 http://dx.doi.org/10.3389/fcell.2020.00525 |
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author | Labusch, Miriam Mancini, Laure Morizet, David Bally-Cuif, Laure |
author_facet | Labusch, Miriam Mancini, Laure Morizet, David Bally-Cuif, Laure |
author_sort | Labusch, Miriam |
collection | PubMed |
description | Adult neurogenesis, i.e., the generation of neurons from neural stem cells (NSCs) in the adult brain, contributes to brain plasticity in all vertebrates. It varies, however, greatly in extent, location and physiological characteristics between species. During the last decade, the teleost zebrafish (D. rerio) was increasingly used to study the molecular and cellular properties of adult NSCs, in particular as a prominent NSC population was discovered at the ventricular surface of the dorsal telencephalon (pallium), in territories homologous to the adult neurogenic niches of rodents. This model, for its specific features (large NSC population, amenability to intravital imaging, high regenerative capacity) allowed rapid progress in the characterization of basic adult NSC features. We review here these findings, with specific comparisons with the situation in rodents. We specifically discuss the cellular nature of NSCs (astroglial or neuroepithelial cells), their heterogeneities and their neurogenic lineages, and the mechanisms controlling NSC quiescence and fate choices, which all impact the neurogenic output. We further discuss the regulation of NSC activity in response to physiological triggers and non-physiological conditions such as regenerative contexts. |
format | Online Article Text |
id | pubmed-7338623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73386232020-07-20 Conserved and Divergent Features of Adult Neurogenesis in Zebrafish Labusch, Miriam Mancini, Laure Morizet, David Bally-Cuif, Laure Front Cell Dev Biol Cell and Developmental Biology Adult neurogenesis, i.e., the generation of neurons from neural stem cells (NSCs) in the adult brain, contributes to brain plasticity in all vertebrates. It varies, however, greatly in extent, location and physiological characteristics between species. During the last decade, the teleost zebrafish (D. rerio) was increasingly used to study the molecular and cellular properties of adult NSCs, in particular as a prominent NSC population was discovered at the ventricular surface of the dorsal telencephalon (pallium), in territories homologous to the adult neurogenic niches of rodents. This model, for its specific features (large NSC population, amenability to intravital imaging, high regenerative capacity) allowed rapid progress in the characterization of basic adult NSC features. We review here these findings, with specific comparisons with the situation in rodents. We specifically discuss the cellular nature of NSCs (astroglial or neuroepithelial cells), their heterogeneities and their neurogenic lineages, and the mechanisms controlling NSC quiescence and fate choices, which all impact the neurogenic output. We further discuss the regulation of NSC activity in response to physiological triggers and non-physiological conditions such as regenerative contexts. Frontiers Media S.A. 2020-06-30 /pmc/articles/PMC7338623/ /pubmed/32695781 http://dx.doi.org/10.3389/fcell.2020.00525 Text en Copyright © 2020 Labusch, Mancini, Morizet and Bally-Cuif. 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) and the copyright owner(s) 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 | Cell and Developmental Biology Labusch, Miriam Mancini, Laure Morizet, David Bally-Cuif, Laure Conserved and Divergent Features of Adult Neurogenesis in Zebrafish |
title | Conserved and Divergent Features of Adult Neurogenesis in Zebrafish |
title_full | Conserved and Divergent Features of Adult Neurogenesis in Zebrafish |
title_fullStr | Conserved and Divergent Features of Adult Neurogenesis in Zebrafish |
title_full_unstemmed | Conserved and Divergent Features of Adult Neurogenesis in Zebrafish |
title_short | Conserved and Divergent Features of Adult Neurogenesis in Zebrafish |
title_sort | conserved and divergent features of adult neurogenesis in zebrafish |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338623/ https://www.ncbi.nlm.nih.gov/pubmed/32695781 http://dx.doi.org/10.3389/fcell.2020.00525 |
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