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Human spinal cord in vitro differentiation pace is initially maintained in heterologous embryonic environments
Species-specific differentiation pace in vitro indicates that some aspects of neural differentiation are governed by cell intrinsic properties. Here we describe a novel in vitro human neural-rosette assay that recapitulates dorsal spinal cord differentiation but proceeds more rapidly than in the hum...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8929931/ https://www.ncbi.nlm.nih.gov/pubmed/35188104 http://dx.doi.org/10.7554/eLife.67283 |
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author | Dady, Alwyn Davidson, Lindsay Halley, Pamela A Storey, Kate G |
author_facet | Dady, Alwyn Davidson, Lindsay Halley, Pamela A Storey, Kate G |
author_sort | Dady, Alwyn |
collection | PubMed |
description | Species-specific differentiation pace in vitro indicates that some aspects of neural differentiation are governed by cell intrinsic properties. Here we describe a novel in vitro human neural-rosette assay that recapitulates dorsal spinal cord differentiation but proceeds more rapidly than in the human embryo, suggesting that it lacks endogenous signalling dynamics. To test whether in vitro conditions represent an intrinsic differentiation pace, human iPSC-derived neural rosettes were challenged by grafting into the faster differentiating chicken embryonic neural tube iso-chronically, or hetero-chronically into older embryos. In both contexts in vitro differentiation pace was initially unchanged, while long-term analysis revealed iso-chronic slowed and hetero-chronic conditions promoted human neural differentiation. Moreover, hetero-chronic conditions did not alter the human neural differentiation programme, which progressed to neurogenesis, while the host embryo advanced into gliogenesis. This study demonstrates that intrinsic properties limit human differentiation pace, and that timely extrinsic signals are required for progression through an intrinsic human neural differentiation programme. |
format | Online Article Text |
id | pubmed-8929931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-89299312022-03-18 Human spinal cord in vitro differentiation pace is initially maintained in heterologous embryonic environments Dady, Alwyn Davidson, Lindsay Halley, Pamela A Storey, Kate G eLife Developmental Biology Species-specific differentiation pace in vitro indicates that some aspects of neural differentiation are governed by cell intrinsic properties. Here we describe a novel in vitro human neural-rosette assay that recapitulates dorsal spinal cord differentiation but proceeds more rapidly than in the human embryo, suggesting that it lacks endogenous signalling dynamics. To test whether in vitro conditions represent an intrinsic differentiation pace, human iPSC-derived neural rosettes were challenged by grafting into the faster differentiating chicken embryonic neural tube iso-chronically, or hetero-chronically into older embryos. In both contexts in vitro differentiation pace was initially unchanged, while long-term analysis revealed iso-chronic slowed and hetero-chronic conditions promoted human neural differentiation. Moreover, hetero-chronic conditions did not alter the human neural differentiation programme, which progressed to neurogenesis, while the host embryo advanced into gliogenesis. This study demonstrates that intrinsic properties limit human differentiation pace, and that timely extrinsic signals are required for progression through an intrinsic human neural differentiation programme. eLife Sciences Publications, Ltd 2022-02-21 /pmc/articles/PMC8929931/ /pubmed/35188104 http://dx.doi.org/10.7554/eLife.67283 Text en © 2022, Dady et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Dady, Alwyn Davidson, Lindsay Halley, Pamela A Storey, Kate G Human spinal cord in vitro differentiation pace is initially maintained in heterologous embryonic environments |
title | Human spinal cord in vitro differentiation pace is initially maintained in heterologous embryonic environments |
title_full | Human spinal cord in vitro differentiation pace is initially maintained in heterologous embryonic environments |
title_fullStr | Human spinal cord in vitro differentiation pace is initially maintained in heterologous embryonic environments |
title_full_unstemmed | Human spinal cord in vitro differentiation pace is initially maintained in heterologous embryonic environments |
title_short | Human spinal cord in vitro differentiation pace is initially maintained in heterologous embryonic environments |
title_sort | human spinal cord in vitro differentiation pace is initially maintained in heterologous embryonic environments |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8929931/ https://www.ncbi.nlm.nih.gov/pubmed/35188104 http://dx.doi.org/10.7554/eLife.67283 |
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