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The diversity of trophoblast cells and niches of placenta accreta spectrum disorders revealed by single-cell RNA sequencing
Placenta accreta spectrum disorders (PAS) are severe pregnancy complications that occur when extravillous trophoblast cells (EVTs) invade beyond the uterine inner myometrium and are characterized by hypervascularity on prenatal ultrasound and catastrophic postpartum hemorrhage. The potential mechani...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676682/ https://www.ncbi.nlm.nih.gov/pubmed/36420138 http://dx.doi.org/10.3389/fcell.2022.1044198 |
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author | Ma, Jingmei Liu, Yawei Guo, Zhirong Sun, Run Yang, Xinrui Zheng, Weiran Ma, Yongdan Rong, Yin Wang, Hongmei Yang, Huixia Xiao, Zhenyu |
author_facet | Ma, Jingmei Liu, Yawei Guo, Zhirong Sun, Run Yang, Xinrui Zheng, Weiran Ma, Yongdan Rong, Yin Wang, Hongmei Yang, Huixia Xiao, Zhenyu |
author_sort | Ma, Jingmei |
collection | PubMed |
description | Placenta accreta spectrum disorders (PAS) are severe pregnancy complications that occur when extravillous trophoblast cells (EVTs) invade beyond the uterine inner myometrium and are characterized by hypervascularity on prenatal ultrasound and catastrophic postpartum hemorrhage. The potential mechanisms remain incompletely understood. With single-cell RNA-sequencing analysis on the representative invasive parts and the normal part obtained from the same PAS placenta, we profiled the pathological landscape of invasive PAS placenta and deciphered an intensified differentiation pathway from progenitor cytotrophoblasts (CTBs) to EVTs via LAMB4 ( + ) and KRT6A ( + ) CTBs. In the absence of the decidua, the invasive trophoblasts of various differentiation states interacted with ADIRF ( + ) and DES ( + ) maternal stromal cells. The PAS-associated hypervascularity might be due to the enhanced crosstalk of trophoblasts, stromal cells and vascular endothelial cells. Finally, we presented an immune microenvironmental landscape of invasive PAS. The pathogenesis of PAS could be further explored with current resources for future targeted translational studies. |
format | Online Article Text |
id | pubmed-9676682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96766822022-11-22 The diversity of trophoblast cells and niches of placenta accreta spectrum disorders revealed by single-cell RNA sequencing Ma, Jingmei Liu, Yawei Guo, Zhirong Sun, Run Yang, Xinrui Zheng, Weiran Ma, Yongdan Rong, Yin Wang, Hongmei Yang, Huixia Xiao, Zhenyu Front Cell Dev Biol Cell and Developmental Biology Placenta accreta spectrum disorders (PAS) are severe pregnancy complications that occur when extravillous trophoblast cells (EVTs) invade beyond the uterine inner myometrium and are characterized by hypervascularity on prenatal ultrasound and catastrophic postpartum hemorrhage. The potential mechanisms remain incompletely understood. With single-cell RNA-sequencing analysis on the representative invasive parts and the normal part obtained from the same PAS placenta, we profiled the pathological landscape of invasive PAS placenta and deciphered an intensified differentiation pathway from progenitor cytotrophoblasts (CTBs) to EVTs via LAMB4 ( + ) and KRT6A ( + ) CTBs. In the absence of the decidua, the invasive trophoblasts of various differentiation states interacted with ADIRF ( + ) and DES ( + ) maternal stromal cells. The PAS-associated hypervascularity might be due to the enhanced crosstalk of trophoblasts, stromal cells and vascular endothelial cells. Finally, we presented an immune microenvironmental landscape of invasive PAS. The pathogenesis of PAS could be further explored with current resources for future targeted translational studies. Frontiers Media S.A. 2022-11-07 /pmc/articles/PMC9676682/ /pubmed/36420138 http://dx.doi.org/10.3389/fcell.2022.1044198 Text en Copyright © 2022 Ma, Liu, Guo, Sun, Yang, Zheng, Ma, Rong, Wang, Yang and Xiao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Ma, Jingmei Liu, Yawei Guo, Zhirong Sun, Run Yang, Xinrui Zheng, Weiran Ma, Yongdan Rong, Yin Wang, Hongmei Yang, Huixia Xiao, Zhenyu The diversity of trophoblast cells and niches of placenta accreta spectrum disorders revealed by single-cell RNA sequencing |
title | The diversity of trophoblast cells and niches of placenta accreta spectrum disorders revealed by single-cell RNA sequencing |
title_full | The diversity of trophoblast cells and niches of placenta accreta spectrum disorders revealed by single-cell RNA sequencing |
title_fullStr | The diversity of trophoblast cells and niches of placenta accreta spectrum disorders revealed by single-cell RNA sequencing |
title_full_unstemmed | The diversity of trophoblast cells and niches of placenta accreta spectrum disorders revealed by single-cell RNA sequencing |
title_short | The diversity of trophoblast cells and niches of placenta accreta spectrum disorders revealed by single-cell RNA sequencing |
title_sort | diversity of trophoblast cells and niches of placenta accreta spectrum disorders revealed by single-cell rna sequencing |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676682/ https://www.ncbi.nlm.nih.gov/pubmed/36420138 http://dx.doi.org/10.3389/fcell.2022.1044198 |
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