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Single-cell analysis of mouse uterus at the invasion phase of embryo implantation
BACKGROUND: Embryo implantation into the uterus is a crucial step for human reproduction. A hypothesis has been proposed that the molecular circuit invented by trophoblasts for invasive embryo implantation during evolution might be misused by cancer cells to promote malignancy. Unfortunately, our cu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8817544/ https://www.ncbi.nlm.nih.gov/pubmed/35123575 http://dx.doi.org/10.1186/s13578-022-00749-y |
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author | He, Jia-Peng Tian, Qing Zhu, Qiu-Yang Liu, Ji-Long |
author_facet | He, Jia-Peng Tian, Qing Zhu, Qiu-Yang Liu, Ji-Long |
author_sort | He, Jia-Peng |
collection | PubMed |
description | BACKGROUND: Embryo implantation into the uterus is a crucial step for human reproduction. A hypothesis has been proposed that the molecular circuit invented by trophoblasts for invasive embryo implantation during evolution might be misused by cancer cells to promote malignancy. Unfortunately, our current understanding of the molecular mechanism underlying embryo implantation is far from complete. RESULTS: Here we used the mouse as an animal model and generated a single-cell transcriptomic atlas of the embryo implantation site of mouse uterus at the invasion phase of embryo implantation on gestational day 6. We revealed 23 distinct cell clusters, including 5 stromal cell clusters, 2 epithelial cell clusters, 1 smooth muscle cell cluster, 2 pericyte clusters, 4 endothelial cell clusters, and 9 immune cell clusters. Through data analysis, we identified differentially expression changes in all uterine cell types upon embryo implantation. By integrated with single-cell RNA-seq data from E5.5 embryos, we predicted cell–cell crosstalk between trophoblasts and uterine cell types. CONCLUSIONS: Our study provides a valuable resource for understanding of the molecular mechanism of embryo implantation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-022-00749-y. |
format | Online Article Text |
id | pubmed-8817544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88175442022-02-07 Single-cell analysis of mouse uterus at the invasion phase of embryo implantation He, Jia-Peng Tian, Qing Zhu, Qiu-Yang Liu, Ji-Long Cell Biosci Research BACKGROUND: Embryo implantation into the uterus is a crucial step for human reproduction. A hypothesis has been proposed that the molecular circuit invented by trophoblasts for invasive embryo implantation during evolution might be misused by cancer cells to promote malignancy. Unfortunately, our current understanding of the molecular mechanism underlying embryo implantation is far from complete. RESULTS: Here we used the mouse as an animal model and generated a single-cell transcriptomic atlas of the embryo implantation site of mouse uterus at the invasion phase of embryo implantation on gestational day 6. We revealed 23 distinct cell clusters, including 5 stromal cell clusters, 2 epithelial cell clusters, 1 smooth muscle cell cluster, 2 pericyte clusters, 4 endothelial cell clusters, and 9 immune cell clusters. Through data analysis, we identified differentially expression changes in all uterine cell types upon embryo implantation. By integrated with single-cell RNA-seq data from E5.5 embryos, we predicted cell–cell crosstalk between trophoblasts and uterine cell types. CONCLUSIONS: Our study provides a valuable resource for understanding of the molecular mechanism of embryo implantation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-022-00749-y. BioMed Central 2022-02-05 /pmc/articles/PMC8817544/ /pubmed/35123575 http://dx.doi.org/10.1186/s13578-022-00749-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research He, Jia-Peng Tian, Qing Zhu, Qiu-Yang Liu, Ji-Long Single-cell analysis of mouse uterus at the invasion phase of embryo implantation |
title | Single-cell analysis of mouse uterus at the invasion phase of embryo implantation |
title_full | Single-cell analysis of mouse uterus at the invasion phase of embryo implantation |
title_fullStr | Single-cell analysis of mouse uterus at the invasion phase of embryo implantation |
title_full_unstemmed | Single-cell analysis of mouse uterus at the invasion phase of embryo implantation |
title_short | Single-cell analysis of mouse uterus at the invasion phase of embryo implantation |
title_sort | single-cell analysis of mouse uterus at the invasion phase of embryo implantation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8817544/ https://www.ncbi.nlm.nih.gov/pubmed/35123575 http://dx.doi.org/10.1186/s13578-022-00749-y |
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