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Self‐assembled human placental model from trophoblast stem cells in a dynamic organ‐on‐a‐chip system

The placental barrier plays a key role in protecting the developing fetus from xenobiotics and exchanging substances between the fetus and mother. However, the trophoblast cell lines and animal models are often inadequate to recapitulate the key architecture and functional characteristics of human p...

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Autores principales: Cao, Rongkai, Wang, Yaqing, Liu, Jiayue, Rong, Lujuan, Qin, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212715/
https://www.ncbi.nlm.nih.gov/pubmed/37199016
http://dx.doi.org/10.1111/cpr.13469
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author Cao, Rongkai
Wang, Yaqing
Liu, Jiayue
Rong, Lujuan
Qin, Jianhua
author_facet Cao, Rongkai
Wang, Yaqing
Liu, Jiayue
Rong, Lujuan
Qin, Jianhua
author_sort Cao, Rongkai
collection PubMed
description The placental barrier plays a key role in protecting the developing fetus from xenobiotics and exchanging substances between the fetus and mother. However, the trophoblast cell lines and animal models are often inadequate to recapitulate the key architecture and functional characteristics of human placental barrier. Here, we described a biomimetic placental barrier model from human trophoblast stem cells (hTSCs) in a perfused organ chip system. The placental barrier was constructed by co‐culture of hTSCs and endothelial cells on the opposite sides of a collagen‐coated membrane on chip. hTSCs can differentiate into cytotrophoblasts (CT) and syncytiotrophoblast (ST), which self‐assembled into bilayered trophoblastic epithelium with placental microvilli‐like structure under dynamic cultures. The formed placental barrier displayed dense microvilli, higher level secretion of human chorionic gonadotropin (hCG), enhanced glucose transport activity. Moreover, RNA‐seq analysis revealed upregulated ST expression and activation of trophoblast differentiation‐related signalling pathways. These results indicated the key role of fluid flow in promoting trophoblast syncytialization and placental early development. After exposure to mono‐2‐ethylhexyl phthalate, one of the endocrine disrupting chemicals, the model showed inhibited hCG production and disturbed ST formation in trophoblastic epithelium, suggesting impaired placental structure and function elicited by environmental toxicants. Collectively, the hTSCs‐derived placental model can recapitulate placenta physiology and pathological response to external stimuli in a biomimetic manner, which is useful for the study of placental biology and associated diseases.
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spelling pubmed-102127152023-05-27 Self‐assembled human placental model from trophoblast stem cells in a dynamic organ‐on‐a‐chip system Cao, Rongkai Wang, Yaqing Liu, Jiayue Rong, Lujuan Qin, Jianhua Cell Prolif Original Articles The placental barrier plays a key role in protecting the developing fetus from xenobiotics and exchanging substances between the fetus and mother. However, the trophoblast cell lines and animal models are often inadequate to recapitulate the key architecture and functional characteristics of human placental barrier. Here, we described a biomimetic placental barrier model from human trophoblast stem cells (hTSCs) in a perfused organ chip system. The placental barrier was constructed by co‐culture of hTSCs and endothelial cells on the opposite sides of a collagen‐coated membrane on chip. hTSCs can differentiate into cytotrophoblasts (CT) and syncytiotrophoblast (ST), which self‐assembled into bilayered trophoblastic epithelium with placental microvilli‐like structure under dynamic cultures. The formed placental barrier displayed dense microvilli, higher level secretion of human chorionic gonadotropin (hCG), enhanced glucose transport activity. Moreover, RNA‐seq analysis revealed upregulated ST expression and activation of trophoblast differentiation‐related signalling pathways. These results indicated the key role of fluid flow in promoting trophoblast syncytialization and placental early development. After exposure to mono‐2‐ethylhexyl phthalate, one of the endocrine disrupting chemicals, the model showed inhibited hCG production and disturbed ST formation in trophoblastic epithelium, suggesting impaired placental structure and function elicited by environmental toxicants. Collectively, the hTSCs‐derived placental model can recapitulate placenta physiology and pathological response to external stimuli in a biomimetic manner, which is useful for the study of placental biology and associated diseases. John Wiley and Sons Inc. 2023-05-17 /pmc/articles/PMC10212715/ /pubmed/37199016 http://dx.doi.org/10.1111/cpr.13469 Text en © 2023 The Authors. Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Cao, Rongkai
Wang, Yaqing
Liu, Jiayue
Rong, Lujuan
Qin, Jianhua
Self‐assembled human placental model from trophoblast stem cells in a dynamic organ‐on‐a‐chip system
title Self‐assembled human placental model from trophoblast stem cells in a dynamic organ‐on‐a‐chip system
title_full Self‐assembled human placental model from trophoblast stem cells in a dynamic organ‐on‐a‐chip system
title_fullStr Self‐assembled human placental model from trophoblast stem cells in a dynamic organ‐on‐a‐chip system
title_full_unstemmed Self‐assembled human placental model from trophoblast stem cells in a dynamic organ‐on‐a‐chip system
title_short Self‐assembled human placental model from trophoblast stem cells in a dynamic organ‐on‐a‐chip system
title_sort self‐assembled human placental model from trophoblast stem cells in a dynamic organ‐on‐a‐chip system
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212715/
https://www.ncbi.nlm.nih.gov/pubmed/37199016
http://dx.doi.org/10.1111/cpr.13469
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