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Single-cell RNA-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta
The placenta is crucial for a successful pregnancy and the health of both the fetus and the pregnant woman. However, how the human trophoblast lineage is regulated, including the categorization of the placental cell subtypes is poorly understood. Here we performed single-cell RNA sequencing (RNA-seq...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082907/ https://www.ncbi.nlm.nih.gov/pubmed/30042384 http://dx.doi.org/10.1038/s41422-018-0066-y |
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author | Liu, Yawei Fan, Xiaoying Wang, Rui Lu, Xiaoyin Dang, Yan-Li Wang, Huiying Lin, Hai-Yan Zhu, Cheng Ge, Hao Cross, James C. Wang, Hongmei |
author_facet | Liu, Yawei Fan, Xiaoying Wang, Rui Lu, Xiaoyin Dang, Yan-Li Wang, Huiying Lin, Hai-Yan Zhu, Cheng Ge, Hao Cross, James C. Wang, Hongmei |
author_sort | Liu, Yawei |
collection | PubMed |
description | The placenta is crucial for a successful pregnancy and the health of both the fetus and the pregnant woman. However, how the human trophoblast lineage is regulated, including the categorization of the placental cell subtypes is poorly understood. Here we performed single-cell RNA sequencing (RNA-seq) on sorted placental cells from first- and second-trimester human placentas. New subtypes of cells of the known cytotrophoblast cells (CTBs), extravillous trophoblast cells (EVTs), Hofbauer cells, and mesenchymal stromal cells were identified and cell-type-specific gene signatures were defined. Functionally, this study revealed many previously unknown functions of the human placenta. Notably, 102 polypeptide hormone genes were found to be expressed by various subtypes of placental cells, which suggests a complex and significant role of these hormones in regulating fetal growth and adaptations of maternal physiology to pregnancy. These results document human placental trophoblast differentiation at single-cell resolution and thus advance our understanding of human placentation during the early stage of pregnancy. |
format | Online Article Text |
id | pubmed-6082907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60829072018-08-09 Single-cell RNA-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta Liu, Yawei Fan, Xiaoying Wang, Rui Lu, Xiaoyin Dang, Yan-Li Wang, Huiying Lin, Hai-Yan Zhu, Cheng Ge, Hao Cross, James C. Wang, Hongmei Cell Res Article The placenta is crucial for a successful pregnancy and the health of both the fetus and the pregnant woman. However, how the human trophoblast lineage is regulated, including the categorization of the placental cell subtypes is poorly understood. Here we performed single-cell RNA sequencing (RNA-seq) on sorted placental cells from first- and second-trimester human placentas. New subtypes of cells of the known cytotrophoblast cells (CTBs), extravillous trophoblast cells (EVTs), Hofbauer cells, and mesenchymal stromal cells were identified and cell-type-specific gene signatures were defined. Functionally, this study revealed many previously unknown functions of the human placenta. Notably, 102 polypeptide hormone genes were found to be expressed by various subtypes of placental cells, which suggests a complex and significant role of these hormones in regulating fetal growth and adaptations of maternal physiology to pregnancy. These results document human placental trophoblast differentiation at single-cell resolution and thus advance our understanding of human placentation during the early stage of pregnancy. Nature Publishing Group UK 2018-07-24 2018-08 /pmc/articles/PMC6082907/ /pubmed/30042384 http://dx.doi.org/10.1038/s41422-018-0066-y Text en © IBCB, SIBS, CAS 2018 Open Access This article is licensed under. 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. 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. 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. copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Liu, Yawei Fan, Xiaoying Wang, Rui Lu, Xiaoyin Dang, Yan-Li Wang, Huiying Lin, Hai-Yan Zhu, Cheng Ge, Hao Cross, James C. Wang, Hongmei Single-cell RNA-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta |
title | Single-cell RNA-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta |
title_full | Single-cell RNA-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta |
title_fullStr | Single-cell RNA-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta |
title_full_unstemmed | Single-cell RNA-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta |
title_short | Single-cell RNA-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta |
title_sort | single-cell rna-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082907/ https://www.ncbi.nlm.nih.gov/pubmed/30042384 http://dx.doi.org/10.1038/s41422-018-0066-y |
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