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Identification of a rare Gli1(+) progenitor cell population contributing to liver regeneration during chronic injury
In adults, hepatocytes are mainly replenished from the existing progenitor pools of hepatocytes and cholangiocytes during chronic liver injury. However, it is unclear whether other cell types in addition to classical hepatocytes and cholangiocytes contribute to hepatocyte regeneration after chronic...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622734/ https://www.ncbi.nlm.nih.gov/pubmed/36316325 http://dx.doi.org/10.1038/s41421-022-00474-3 |
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author | Peng, Jiayin Li, Fei Wang, Jia Wang, Chaoxiong Jiang, Yiao Liu, Biao He, Juan Yuan, Kai Pan, Chenyu Lin, Moubin Zhou, Bin Chen, Luonan Gao, Dong Zhao, Yun |
author_facet | Peng, Jiayin Li, Fei Wang, Jia Wang, Chaoxiong Jiang, Yiao Liu, Biao He, Juan Yuan, Kai Pan, Chenyu Lin, Moubin Zhou, Bin Chen, Luonan Gao, Dong Zhao, Yun |
author_sort | Peng, Jiayin |
collection | PubMed |
description | In adults, hepatocytes are mainly replenished from the existing progenitor pools of hepatocytes and cholangiocytes during chronic liver injury. However, it is unclear whether other cell types in addition to classical hepatocytes and cholangiocytes contribute to hepatocyte regeneration after chronic liver injuries. Here, we identified a new biphenotypic cell population that contributes to hepatocyte regeneration during chronic liver injuries. We found that a cell population expressed Gli1 and EpCAM (EpCAM(+)Gli1(+)), which was further characterized with both epithelial and mesenchymal identities by single-cell RNA sequencing. Genetic lineage tracing using dual recombinases revealed that Gli1(+) nonhepatocyte cell population could generate hepatocytes after chronic liver injury. EpCAM(+)Gli1(+) cells exhibited a greater capacity for organoid formation with functional hepatocytes in vitro and liver regeneration upon transplantation in vivo. Collectively, these findings demonstrate that EpCAM(+)Gli1(+) cells can serve as a new source of liver progenitor cells and contribute to liver repair and regeneration. |
format | Online Article Text |
id | pubmed-9622734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-96227342022-11-02 Identification of a rare Gli1(+) progenitor cell population contributing to liver regeneration during chronic injury Peng, Jiayin Li, Fei Wang, Jia Wang, Chaoxiong Jiang, Yiao Liu, Biao He, Juan Yuan, Kai Pan, Chenyu Lin, Moubin Zhou, Bin Chen, Luonan Gao, Dong Zhao, Yun Cell Discov Article In adults, hepatocytes are mainly replenished from the existing progenitor pools of hepatocytes and cholangiocytes during chronic liver injury. However, it is unclear whether other cell types in addition to classical hepatocytes and cholangiocytes contribute to hepatocyte regeneration after chronic liver injuries. Here, we identified a new biphenotypic cell population that contributes to hepatocyte regeneration during chronic liver injuries. We found that a cell population expressed Gli1 and EpCAM (EpCAM(+)Gli1(+)), which was further characterized with both epithelial and mesenchymal identities by single-cell RNA sequencing. Genetic lineage tracing using dual recombinases revealed that Gli1(+) nonhepatocyte cell population could generate hepatocytes after chronic liver injury. EpCAM(+)Gli1(+) cells exhibited a greater capacity for organoid formation with functional hepatocytes in vitro and liver regeneration upon transplantation in vivo. Collectively, these findings demonstrate that EpCAM(+)Gli1(+) cells can serve as a new source of liver progenitor cells and contribute to liver repair and regeneration. Springer Nature Singapore 2022-11-01 /pmc/articles/PMC9622734/ /pubmed/36316325 http://dx.doi.org/10.1038/s41421-022-00474-3 Text en © The Author(s) 2022 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 Peng, Jiayin Li, Fei Wang, Jia Wang, Chaoxiong Jiang, Yiao Liu, Biao He, Juan Yuan, Kai Pan, Chenyu Lin, Moubin Zhou, Bin Chen, Luonan Gao, Dong Zhao, Yun Identification of a rare Gli1(+) progenitor cell population contributing to liver regeneration during chronic injury |
title | Identification of a rare Gli1(+) progenitor cell population contributing to liver regeneration during chronic injury |
title_full | Identification of a rare Gli1(+) progenitor cell population contributing to liver regeneration during chronic injury |
title_fullStr | Identification of a rare Gli1(+) progenitor cell population contributing to liver regeneration during chronic injury |
title_full_unstemmed | Identification of a rare Gli1(+) progenitor cell population contributing to liver regeneration during chronic injury |
title_short | Identification of a rare Gli1(+) progenitor cell population contributing to liver regeneration during chronic injury |
title_sort | identification of a rare gli1(+) progenitor cell population contributing to liver regeneration during chronic injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622734/ https://www.ncbi.nlm.nih.gov/pubmed/36316325 http://dx.doi.org/10.1038/s41421-022-00474-3 |
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