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A differentiation roadmap of murine placentation at single-cell resolution
The placenta is one of the most important yet least understood organs. Due to the limitations of conventional research approaches, we are still far from a comprehensive understanding of mouse placentation, especially regarding the differentiation of trophoblast lineages at the early developmental st...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020559/ https://www.ncbi.nlm.nih.gov/pubmed/36928215 http://dx.doi.org/10.1038/s41421-022-00513-z |
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author | Jiang, Xiangxiang Wang, Yue Xiao, Zhenyu Yan, Long Guo, Shanshan Wang, Yiming Wu, Hao Zhao, Xuehan Lu, Xiaoyin Wang, Hongmei |
author_facet | Jiang, Xiangxiang Wang, Yue Xiao, Zhenyu Yan, Long Guo, Shanshan Wang, Yiming Wu, Hao Zhao, Xuehan Lu, Xiaoyin Wang, Hongmei |
author_sort | Jiang, Xiangxiang |
collection | PubMed |
description | The placenta is one of the most important yet least understood organs. Due to the limitations of conventional research approaches, we are still far from a comprehensive understanding of mouse placentation, especially regarding the differentiation of trophoblast lineages at the early developmental stage. To decipher cell compositions and developmental processes, we systematically profile the single-cell transcriptomes of trophoblast cells from extraembryonic tissues (embryonic day 7.5 (E7.5) and E8.5) and placentae (E9.5–E14.5) at one-day intervals. We identify distinct trophoblast cell types during mouse placentation, including unreported progenitor cells and intermediate precursor cells. An updated differentiation roadmap of mouse trophoblast lineages is presented following systematic transcriptome analyses. Based on transcriptomic regulatory network inference, we specify transcription factors responsible for the regulation of dynamic developmental processes during lineage diversification. We map lineage differentiation trajectories and find that sinusoid trophoblast giant cells arise from the subpopulation of ectoplacental cone cells. We provide a comprehensive single-cell data resource to shed light on future mechanistic studies of the gene regulatory networks governing hemochorial placentation. |
format | Online Article Text |
id | pubmed-10020559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-100205592023-03-18 A differentiation roadmap of murine placentation at single-cell resolution Jiang, Xiangxiang Wang, Yue Xiao, Zhenyu Yan, Long Guo, Shanshan Wang, Yiming Wu, Hao Zhao, Xuehan Lu, Xiaoyin Wang, Hongmei Cell Discov Article The placenta is one of the most important yet least understood organs. Due to the limitations of conventional research approaches, we are still far from a comprehensive understanding of mouse placentation, especially regarding the differentiation of trophoblast lineages at the early developmental stage. To decipher cell compositions and developmental processes, we systematically profile the single-cell transcriptomes of trophoblast cells from extraembryonic tissues (embryonic day 7.5 (E7.5) and E8.5) and placentae (E9.5–E14.5) at one-day intervals. We identify distinct trophoblast cell types during mouse placentation, including unreported progenitor cells and intermediate precursor cells. An updated differentiation roadmap of mouse trophoblast lineages is presented following systematic transcriptome analyses. Based on transcriptomic regulatory network inference, we specify transcription factors responsible for the regulation of dynamic developmental processes during lineage diversification. We map lineage differentiation trajectories and find that sinusoid trophoblast giant cells arise from the subpopulation of ectoplacental cone cells. We provide a comprehensive single-cell data resource to shed light on future mechanistic studies of the gene regulatory networks governing hemochorial placentation. Springer Nature Singapore 2023-03-17 /pmc/articles/PMC10020559/ /pubmed/36928215 http://dx.doi.org/10.1038/s41421-022-00513-z 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 Jiang, Xiangxiang Wang, Yue Xiao, Zhenyu Yan, Long Guo, Shanshan Wang, Yiming Wu, Hao Zhao, Xuehan Lu, Xiaoyin Wang, Hongmei A differentiation roadmap of murine placentation at single-cell resolution |
title | A differentiation roadmap of murine placentation at single-cell resolution |
title_full | A differentiation roadmap of murine placentation at single-cell resolution |
title_fullStr | A differentiation roadmap of murine placentation at single-cell resolution |
title_full_unstemmed | A differentiation roadmap of murine placentation at single-cell resolution |
title_short | A differentiation roadmap of murine placentation at single-cell resolution |
title_sort | differentiation roadmap of murine placentation at single-cell resolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020559/ https://www.ncbi.nlm.nih.gov/pubmed/36928215 http://dx.doi.org/10.1038/s41421-022-00513-z |
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