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Neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics
During gastrulation, embryonic cells become specified into distinct germ layers. In mouse, this continues throughout somitogenesis from a population of bipotent stem cells called neuromesodermal progenitors (NMps). However, the degree of self-renewal associated with NMps in the fast-developing zebra...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240315/ https://www.ncbi.nlm.nih.gov/pubmed/30333213 http://dx.doi.org/10.1242/dev.166728 |
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author | Attardi, Andrea Fulton, Timothy Florescu, Maria Shah, Gopi Muresan, Leila Lenz, Martin O. Lancaster, Courtney Huisken, Jan van Oudenaarden, Alexander Steventon, Benjamin |
author_facet | Attardi, Andrea Fulton, Timothy Florescu, Maria Shah, Gopi Muresan, Leila Lenz, Martin O. Lancaster, Courtney Huisken, Jan van Oudenaarden, Alexander Steventon, Benjamin |
author_sort | Attardi, Andrea |
collection | PubMed |
description | During gastrulation, embryonic cells become specified into distinct germ layers. In mouse, this continues throughout somitogenesis from a population of bipotent stem cells called neuromesodermal progenitors (NMps). However, the degree of self-renewal associated with NMps in the fast-developing zebrafish embryo is unclear. Using a genetic clone-tracing method, we labelled early embryonic progenitors and found a strong clonal similarity between spinal cord and mesoderm tissues. We followed individual cell lineages using light-sheet imaging, revealing a common neuromesodermal lineage contribution to a subset of spinal cord tissue across the anterior-posterior body axis. An initial population subdivides at mid-gastrula stages and is directly allocated to neural and mesodermal compartments during gastrulation. A second population in the tailbud undergoes delayed allocation to contribute to the neural and mesodermal compartment only at late somitogenesis. Cell tracking and retrospective cell fate assignment at late somitogenesis stages reveal these cells to be a collection of mono-fated progenitors. Our results suggest that NMps are a conserved population of bipotential progenitors, the lineage of which varies in a species-specific manner due to vastly different rates of differentiation and growth. |
format | Online Article Text |
id | pubmed-6240315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-62403152018-11-26 Neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics Attardi, Andrea Fulton, Timothy Florescu, Maria Shah, Gopi Muresan, Leila Lenz, Martin O. Lancaster, Courtney Huisken, Jan van Oudenaarden, Alexander Steventon, Benjamin Development Research Article During gastrulation, embryonic cells become specified into distinct germ layers. In mouse, this continues throughout somitogenesis from a population of bipotent stem cells called neuromesodermal progenitors (NMps). However, the degree of self-renewal associated with NMps in the fast-developing zebrafish embryo is unclear. Using a genetic clone-tracing method, we labelled early embryonic progenitors and found a strong clonal similarity between spinal cord and mesoderm tissues. We followed individual cell lineages using light-sheet imaging, revealing a common neuromesodermal lineage contribution to a subset of spinal cord tissue across the anterior-posterior body axis. An initial population subdivides at mid-gastrula stages and is directly allocated to neural and mesodermal compartments during gastrulation. A second population in the tailbud undergoes delayed allocation to contribute to the neural and mesodermal compartment only at late somitogenesis. Cell tracking and retrospective cell fate assignment at late somitogenesis stages reveal these cells to be a collection of mono-fated progenitors. Our results suggest that NMps are a conserved population of bipotential progenitors, the lineage of which varies in a species-specific manner due to vastly different rates of differentiation and growth. The Company of Biologists Ltd 2018-11-01 2018-11-09 /pmc/articles/PMC6240315/ /pubmed/30333213 http://dx.doi.org/10.1242/dev.166728 Text en © 2018. 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 (http://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 | Research Article Attardi, Andrea Fulton, Timothy Florescu, Maria Shah, Gopi Muresan, Leila Lenz, Martin O. Lancaster, Courtney Huisken, Jan van Oudenaarden, Alexander Steventon, Benjamin Neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics |
title | Neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics |
title_full | Neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics |
title_fullStr | Neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics |
title_full_unstemmed | Neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics |
title_short | Neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics |
title_sort | neuromesodermal progenitors are a conserved source of spinal cord with divergent growth dynamics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240315/ https://www.ncbi.nlm.nih.gov/pubmed/30333213 http://dx.doi.org/10.1242/dev.166728 |
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