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The temporal transcriptomic signature of cartilage formation
Chondrogenesis is a multistep process, in which cartilage progenitor cells generate a tissue with distinct structural and functional properties. Although several approaches to cartilage regeneration rely on the differentiation of implanted progenitor cells, the temporal transcriptomic landscape of i...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164575/ https://www.ncbi.nlm.nih.gov/pubmed/36987858 http://dx.doi.org/10.1093/nar/gkad210 |
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author | Takács, Roland Vágó, Judit Póliska, Szilárd Pushparaj, Peter Natesan Ducza, László Kovács, Patrik Jin, Eun-Jung Barrett-Jolley, Richard Zákány, Róza Matta, Csaba |
author_facet | Takács, Roland Vágó, Judit Póliska, Szilárd Pushparaj, Peter Natesan Ducza, László Kovács, Patrik Jin, Eun-Jung Barrett-Jolley, Richard Zákány, Róza Matta, Csaba |
author_sort | Takács, Roland |
collection | PubMed |
description | Chondrogenesis is a multistep process, in which cartilage progenitor cells generate a tissue with distinct structural and functional properties. Although several approaches to cartilage regeneration rely on the differentiation of implanted progenitor cells, the temporal transcriptomic landscape of in vitro chondrogenesis in different models has not been reported. Using RNA sequencing, we examined differences in gene expression patterns during cartilage formation in micromass cultures of embryonic limb bud-derived progenitors. Principal component and trajectory analyses revealed a progressively different and distinct transcriptome during chondrogenesis. Differentially expressed genes (DEGs), based on pairwise comparisons of samples from consecutive days were classified into clusters and analysed. We confirmed the involvement of the top DEGs in chondrogenic differentiation using pathway analysis and identified several chondrogenesis-associated transcription factors and collagen subtypes that were not previously linked to cartilage formation. Transient gene silencing of ATOH8 or EBF1 on day 0 attenuated chondrogenesis by deregulating the expression of key osteochondrogenic marker genes in micromass cultures. These results provide detailed insight into the molecular mechanism of chondrogenesis in primary micromass cultures and present a comprehensive dataset of the temporal transcriptomic landscape of chondrogenesis, which may serve as a platform for new molecular approaches in cartilage tissue engineering. |
format | Online Article Text |
id | pubmed-10164575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101645752023-05-08 The temporal transcriptomic signature of cartilage formation Takács, Roland Vágó, Judit Póliska, Szilárd Pushparaj, Peter Natesan Ducza, László Kovács, Patrik Jin, Eun-Jung Barrett-Jolley, Richard Zákány, Róza Matta, Csaba Nucleic Acids Res Data Resources and Analyses Chondrogenesis is a multistep process, in which cartilage progenitor cells generate a tissue with distinct structural and functional properties. Although several approaches to cartilage regeneration rely on the differentiation of implanted progenitor cells, the temporal transcriptomic landscape of in vitro chondrogenesis in different models has not been reported. Using RNA sequencing, we examined differences in gene expression patterns during cartilage formation in micromass cultures of embryonic limb bud-derived progenitors. Principal component and trajectory analyses revealed a progressively different and distinct transcriptome during chondrogenesis. Differentially expressed genes (DEGs), based on pairwise comparisons of samples from consecutive days were classified into clusters and analysed. We confirmed the involvement of the top DEGs in chondrogenic differentiation using pathway analysis and identified several chondrogenesis-associated transcription factors and collagen subtypes that were not previously linked to cartilage formation. Transient gene silencing of ATOH8 or EBF1 on day 0 attenuated chondrogenesis by deregulating the expression of key osteochondrogenic marker genes in micromass cultures. These results provide detailed insight into the molecular mechanism of chondrogenesis in primary micromass cultures and present a comprehensive dataset of the temporal transcriptomic landscape of chondrogenesis, which may serve as a platform for new molecular approaches in cartilage tissue engineering. Oxford University Press 2023-03-29 /pmc/articles/PMC10164575/ /pubmed/36987858 http://dx.doi.org/10.1093/nar/gkad210 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Data Resources and Analyses Takács, Roland Vágó, Judit Póliska, Szilárd Pushparaj, Peter Natesan Ducza, László Kovács, Patrik Jin, Eun-Jung Barrett-Jolley, Richard Zákány, Róza Matta, Csaba The temporal transcriptomic signature of cartilage formation |
title | The temporal transcriptomic signature of cartilage formation |
title_full | The temporal transcriptomic signature of cartilage formation |
title_fullStr | The temporal transcriptomic signature of cartilage formation |
title_full_unstemmed | The temporal transcriptomic signature of cartilage formation |
title_short | The temporal transcriptomic signature of cartilage formation |
title_sort | temporal transcriptomic signature of cartilage formation |
topic | Data Resources and Analyses |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164575/ https://www.ncbi.nlm.nih.gov/pubmed/36987858 http://dx.doi.org/10.1093/nar/gkad210 |
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