Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Attardi, Andrea, Fulton, Timothy, Florescu, Maria, Shah, Gopi, Muresan, Leila, Lenz, Martin O., Lancaster, Courtney, Huisken, Jan, van Oudenaarden, Alexander, Steventon, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2018
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
_version_ 1783371619659415552
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
work_keys_str_mv AT attardiandrea neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics
AT fultontimothy neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics
AT florescumaria neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics
AT shahgopi neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics
AT muresanleila neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics
AT lenzmartino neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics
AT lancastercourtney neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics
AT huiskenjan neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics
AT vanoudenaardenalexander neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics
AT steventonbenjamin neuromesodermalprogenitorsareaconservedsourceofspinalcordwithdivergentgrowthdynamics