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Wnt signaling preserves progenitor cell multipotency during adipose tissue development
Mesenchymal stem/progenitor cells are essential for tissue development and repair throughout life, but how they are maintained under chronic differentiation pressure is not known. Using single-cell transcriptomics of human progenitor cells we find that adipose differentiation stimuli elicit two cell...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290956/ https://www.ncbi.nlm.nih.gov/pubmed/37337125 http://dx.doi.org/10.1038/s42255-023-00813-y |
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author | Yang Loureiro, Zinger Joyce, Shannon DeSouza, Tiffany Solivan-Rivera, Javier Desai, Anand Skritakis, Pantos Yang, Qin Ziegler, Rachel Zhong, Denise Nguyen, Tammy T. MacDougald, Ormond A. Corvera, Silvia |
author_facet | Yang Loureiro, Zinger Joyce, Shannon DeSouza, Tiffany Solivan-Rivera, Javier Desai, Anand Skritakis, Pantos Yang, Qin Ziegler, Rachel Zhong, Denise Nguyen, Tammy T. MacDougald, Ormond A. Corvera, Silvia |
author_sort | Yang Loureiro, Zinger |
collection | PubMed |
description | Mesenchymal stem/progenitor cells are essential for tissue development and repair throughout life, but how they are maintained under chronic differentiation pressure is not known. Using single-cell transcriptomics of human progenitor cells we find that adipose differentiation stimuli elicit two cellular trajectories: one toward mature adipocytes and another toward a pool of non-differentiated cells that maintain progenitor characteristics. These cells are induced by transient Wnt pathway activation and express numerous extracellular matrix genes and are therefore named structural Wnt-regulated adipose tissue cells. We find that the genetic signature of structural Wnt-regulated adipose tissue cells is present in adult human adipose tissue and adipose tissue developed from human progenitor cells in mice. Our results suggest a mechanism whereby adipose differentiation occurs concurrently with the maintenance of a mesenchymal progenitor cell pool, ensuring tissue development, repair and appropriate metabolic control over the lifetime. |
format | Online Article Text |
id | pubmed-10290956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102909562023-06-27 Wnt signaling preserves progenitor cell multipotency during adipose tissue development Yang Loureiro, Zinger Joyce, Shannon DeSouza, Tiffany Solivan-Rivera, Javier Desai, Anand Skritakis, Pantos Yang, Qin Ziegler, Rachel Zhong, Denise Nguyen, Tammy T. MacDougald, Ormond A. Corvera, Silvia Nat Metab Article Mesenchymal stem/progenitor cells are essential for tissue development and repair throughout life, but how they are maintained under chronic differentiation pressure is not known. Using single-cell transcriptomics of human progenitor cells we find that adipose differentiation stimuli elicit two cellular trajectories: one toward mature adipocytes and another toward a pool of non-differentiated cells that maintain progenitor characteristics. These cells are induced by transient Wnt pathway activation and express numerous extracellular matrix genes and are therefore named structural Wnt-regulated adipose tissue cells. We find that the genetic signature of structural Wnt-regulated adipose tissue cells is present in adult human adipose tissue and adipose tissue developed from human progenitor cells in mice. Our results suggest a mechanism whereby adipose differentiation occurs concurrently with the maintenance of a mesenchymal progenitor cell pool, ensuring tissue development, repair and appropriate metabolic control over the lifetime. Nature Publishing Group UK 2023-06-19 2023 /pmc/articles/PMC10290956/ /pubmed/37337125 http://dx.doi.org/10.1038/s42255-023-00813-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yang Loureiro, Zinger Joyce, Shannon DeSouza, Tiffany Solivan-Rivera, Javier Desai, Anand Skritakis, Pantos Yang, Qin Ziegler, Rachel Zhong, Denise Nguyen, Tammy T. MacDougald, Ormond A. Corvera, Silvia Wnt signaling preserves progenitor cell multipotency during adipose tissue development |
title | Wnt signaling preserves progenitor cell multipotency during adipose tissue development |
title_full | Wnt signaling preserves progenitor cell multipotency during adipose tissue development |
title_fullStr | Wnt signaling preserves progenitor cell multipotency during adipose tissue development |
title_full_unstemmed | Wnt signaling preserves progenitor cell multipotency during adipose tissue development |
title_short | Wnt signaling preserves progenitor cell multipotency during adipose tissue development |
title_sort | wnt signaling preserves progenitor cell multipotency during adipose tissue development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290956/ https://www.ncbi.nlm.nih.gov/pubmed/37337125 http://dx.doi.org/10.1038/s42255-023-00813-y |
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