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Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain
Zebrafish display widespread and pronounced adult neurogenesis, which is fundamental for their regeneration capability after central nervous system injury. However, the cellular identity and the biological properties of adult newborn neurons are elusive for most brain areas. Here, we have used short...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983714/ https://www.ncbi.nlm.nih.gov/pubmed/31908317 http://dx.doi.org/10.1242/dev.185595 |
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author | Lange, Christian Rost, Fabian Machate, Anja Reinhardt, Susanne Lesche, Matthias Weber, Anke Kuscha, Veronika Dahl, Andreas Rulands, Steffen Brand, Michael |
author_facet | Lange, Christian Rost, Fabian Machate, Anja Reinhardt, Susanne Lesche, Matthias Weber, Anke Kuscha, Veronika Dahl, Andreas Rulands, Steffen Brand, Michael |
author_sort | Lange, Christian |
collection | PubMed |
description | Zebrafish display widespread and pronounced adult neurogenesis, which is fundamental for their regeneration capability after central nervous system injury. However, the cellular identity and the biological properties of adult newborn neurons are elusive for most brain areas. Here, we have used short-term lineage tracing of radial glia progeny to prospectively isolate newborn neurons from the her4.1(+) radial glia lineage in the homeostatic adult forebrain. Transcriptome analysis of radial glia, newborn neurons and mature neurons using single cell sequencing identified distinct transcriptional profiles, including novel markers for each population. Specifically, we detected two separate newborn neuron types, which showed diversity of cell fate commitment and location. Further analyses showed that these cell types are homologous to neurogenic cells in the mammalian brain, identified neurogenic commitment in proliferating radial glia and indicated that glutamatergic projection neurons are generated in the adult zebrafish telencephalon. Thus, we prospectively isolated adult newborn neurons from the adult zebrafish forebrain, identified markers for newborn and mature neurons in the adult brain, and revealed intrinsic heterogeneity among adult newborn neurons and their homology with mammalian adult neurogenic cell types. |
format | Online Article Text |
id | pubmed-6983714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69837142020-01-28 Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain Lange, Christian Rost, Fabian Machate, Anja Reinhardt, Susanne Lesche, Matthias Weber, Anke Kuscha, Veronika Dahl, Andreas Rulands, Steffen Brand, Michael Development Stem Cells and Regeneration Zebrafish display widespread and pronounced adult neurogenesis, which is fundamental for their regeneration capability after central nervous system injury. However, the cellular identity and the biological properties of adult newborn neurons are elusive for most brain areas. Here, we have used short-term lineage tracing of radial glia progeny to prospectively isolate newborn neurons from the her4.1(+) radial glia lineage in the homeostatic adult forebrain. Transcriptome analysis of radial glia, newborn neurons and mature neurons using single cell sequencing identified distinct transcriptional profiles, including novel markers for each population. Specifically, we detected two separate newborn neuron types, which showed diversity of cell fate commitment and location. Further analyses showed that these cell types are homologous to neurogenic cells in the mammalian brain, identified neurogenic commitment in proliferating radial glia and indicated that glutamatergic projection neurons are generated in the adult zebrafish telencephalon. Thus, we prospectively isolated adult newborn neurons from the adult zebrafish forebrain, identified markers for newborn and mature neurons in the adult brain, and revealed intrinsic heterogeneity among adult newborn neurons and their homology with mammalian adult neurogenic cell types. The Company of Biologists Ltd 2020-01-09 /pmc/articles/PMC6983714/ /pubmed/31908317 http://dx.doi.org/10.1242/dev.185595 Text en © 2020. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Stem Cells and Regeneration Lange, Christian Rost, Fabian Machate, Anja Reinhardt, Susanne Lesche, Matthias Weber, Anke Kuscha, Veronika Dahl, Andreas Rulands, Steffen Brand, Michael Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain |
title | Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain |
title_full | Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain |
title_fullStr | Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain |
title_full_unstemmed | Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain |
title_short | Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain |
title_sort | single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain |
topic | Stem Cells and Regeneration |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983714/ https://www.ncbi.nlm.nih.gov/pubmed/31908317 http://dx.doi.org/10.1242/dev.185595 |
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