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A mosaic world: puzzles revealed by adult neural stem cell heterogeneity

Neural stem cells (NSCs) reside in specialized niches in the adult mammalian brain. The ventricular–subventricular zone (V‐SVZ), adjacent to the lateral ventricles, gives rise to olfactory bulb (OB) neurons, and some astrocytes and oligodendrocytes throughout life. In vitro assays have been widely u...

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Detalles Bibliográficos
Autores principales: Chaker, Zayna, Codega, Paolo, Doetsch, Fiona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113677/
https://www.ncbi.nlm.nih.gov/pubmed/27647730
http://dx.doi.org/10.1002/wdev.248
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author Chaker, Zayna
Codega, Paolo
Doetsch, Fiona
author_facet Chaker, Zayna
Codega, Paolo
Doetsch, Fiona
author_sort Chaker, Zayna
collection PubMed
description Neural stem cells (NSCs) reside in specialized niches in the adult mammalian brain. The ventricular–subventricular zone (V‐SVZ), adjacent to the lateral ventricles, gives rise to olfactory bulb (OB) neurons, and some astrocytes and oligodendrocytes throughout life. In vitro assays have been widely used to retrospectively identify NSCs. However, cells that behave as stem cells in vitro do not reflect the identity, diversity, and behavior of NSCs in vivo. Novel tools including fluorescence activated cell sorting, lineage‐tracing, and clonal analysis have uncovered multiple layers of adult V‐SVZ NSC heterogeneity, including proliferation state and regional identity. In light of these findings, we reexamine the concept of adult NSCs, considering heterogeneity as a key parameter for analyzing their dynamics in vivo. V‐SVZ NSCs form a mosaic of quiescent (qNSCs) and activated cells (aNSCs) that reside in regionally distinct microdomains, reflecting their regional embryonic origins, and give rise to specific subtypes of OB interneurons. Prospective purification and transcriptome analysis of qNSCs and aNSCs has illuminated their molecular and functional properties. qNSCs are slowly dividing, have slow kinetics of neurogenesis in vivo, can be recruited to regenerate the V‐SVZ, and only rarely give rise to in vitro colonies. aNSCs are highly proliferative, undergo rapid clonal expansion of the neurogenic lineage in vivo, and readily form in vitro colonies. Key open questions remain about stem cell dynamics in vivo and the lineage relationship between qNSCs and aNSCs under homeostasis and regeneration, as well as context‐dependent plasticity of regionally distinct adult NSCs under different external stimuli. WIREs Dev Biol 2016, 5:640–658. doi: 10.1002/wdev.248 For further resources related to this article, please visit the WIREs website.
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spelling pubmed-51136772016-12-02 A mosaic world: puzzles revealed by adult neural stem cell heterogeneity Chaker, Zayna Codega, Paolo Doetsch, Fiona Wiley Interdiscip Rev Dev Biol Overview Neural stem cells (NSCs) reside in specialized niches in the adult mammalian brain. The ventricular–subventricular zone (V‐SVZ), adjacent to the lateral ventricles, gives rise to olfactory bulb (OB) neurons, and some astrocytes and oligodendrocytes throughout life. In vitro assays have been widely used to retrospectively identify NSCs. However, cells that behave as stem cells in vitro do not reflect the identity, diversity, and behavior of NSCs in vivo. Novel tools including fluorescence activated cell sorting, lineage‐tracing, and clonal analysis have uncovered multiple layers of adult V‐SVZ NSC heterogeneity, including proliferation state and regional identity. In light of these findings, we reexamine the concept of adult NSCs, considering heterogeneity as a key parameter for analyzing their dynamics in vivo. V‐SVZ NSCs form a mosaic of quiescent (qNSCs) and activated cells (aNSCs) that reside in regionally distinct microdomains, reflecting their regional embryonic origins, and give rise to specific subtypes of OB interneurons. Prospective purification and transcriptome analysis of qNSCs and aNSCs has illuminated their molecular and functional properties. qNSCs are slowly dividing, have slow kinetics of neurogenesis in vivo, can be recruited to regenerate the V‐SVZ, and only rarely give rise to in vitro colonies. aNSCs are highly proliferative, undergo rapid clonal expansion of the neurogenic lineage in vivo, and readily form in vitro colonies. Key open questions remain about stem cell dynamics in vivo and the lineage relationship between qNSCs and aNSCs under homeostasis and regeneration, as well as context‐dependent plasticity of regionally distinct adult NSCs under different external stimuli. WIREs Dev Biol 2016, 5:640–658. doi: 10.1002/wdev.248 For further resources related to this article, please visit the WIREs website. John Wiley & Sons, Inc. 2016-09-20 2016 /pmc/articles/PMC5113677/ /pubmed/27647730 http://dx.doi.org/10.1002/wdev.248 Text en © 2016 The Authors. WIREs Developmental Biology published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Overview
Chaker, Zayna
Codega, Paolo
Doetsch, Fiona
A mosaic world: puzzles revealed by adult neural stem cell heterogeneity
title A mosaic world: puzzles revealed by adult neural stem cell heterogeneity
title_full A mosaic world: puzzles revealed by adult neural stem cell heterogeneity
title_fullStr A mosaic world: puzzles revealed by adult neural stem cell heterogeneity
title_full_unstemmed A mosaic world: puzzles revealed by adult neural stem cell heterogeneity
title_short A mosaic world: puzzles revealed by adult neural stem cell heterogeneity
title_sort mosaic world: puzzles revealed by adult neural stem cell heterogeneity
topic Overview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113677/
https://www.ncbi.nlm.nih.gov/pubmed/27647730
http://dx.doi.org/10.1002/wdev.248
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