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Engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells

The placenta is an essential organ that maintains the health of both the fetus and its mother. Understanding the development of human placenta has been hindered by the limitations of existing animal models and monolayer cell cultures. Models that can recapitulate the essential aspects of human place...

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Autores principales: Cui, Kangli, Chen, Tingwei, Zhu, Yujuan, Shi, Yang, Guo, Yaqiong, Qin, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842056/
https://www.ncbi.nlm.nih.gov/pubmed/36684087
http://dx.doi.org/10.1002/btm2.10390
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author Cui, Kangli
Chen, Tingwei
Zhu, Yujuan
Shi, Yang
Guo, Yaqiong
Qin, Jianhua
author_facet Cui, Kangli
Chen, Tingwei
Zhu, Yujuan
Shi, Yang
Guo, Yaqiong
Qin, Jianhua
author_sort Cui, Kangli
collection PubMed
description The placenta is an essential organ that maintains the health of both the fetus and its mother. Understanding the development of human placenta has been hindered by the limitations of existing animal models and monolayer cell cultures. Models that can recapitulate the essential aspects of human placental multicellular components and vasculature are still lacking. Herein, we presented a new strategy to establish placenta‐like organoids with vascular‐like structures from human‐induced pluripotent stem cells in a defined three‐dimensional (3D) culture system. The resulting placenta‐like tissue resembles first‐trimester human placental development in terms of complex placental components and secretory function. The multicellular tissue was characterized by the inclusion of trophoblasts (cytotrophoblasts, syncytiotrophoblasts, extravillous trophoblasts, and other endogenous vascular cells), which were identified by immunofluorescence, flow cytometry analyses, real‐time quantitative reverse transcription polymerase chain reaction and single‐cell RNA‐seq. Moreover, the 3D tissue was able to secrete the placenta‐specific hormone human chorionic gonadotropin β (hCG‐β) and vascular endothelial growth factor A (VEGFA). The tissue responded to the inflammatory factor tumor necrosis factor‐α (TNF‐α) and VEGF receptor inhibitors. This new model system can represent the major features of placental cellular components, and function, which have not been realized in 2D monolayer cultures. The developed tissue system might open new avenues for studying normal early human placental development and its disease states.
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spelling pubmed-98420562023-01-19 Engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells Cui, Kangli Chen, Tingwei Zhu, Yujuan Shi, Yang Guo, Yaqiong Qin, Jianhua Bioeng Transl Med Research Articles The placenta is an essential organ that maintains the health of both the fetus and its mother. Understanding the development of human placenta has been hindered by the limitations of existing animal models and monolayer cell cultures. Models that can recapitulate the essential aspects of human placental multicellular components and vasculature are still lacking. Herein, we presented a new strategy to establish placenta‐like organoids with vascular‐like structures from human‐induced pluripotent stem cells in a defined three‐dimensional (3D) culture system. The resulting placenta‐like tissue resembles first‐trimester human placental development in terms of complex placental components and secretory function. The multicellular tissue was characterized by the inclusion of trophoblasts (cytotrophoblasts, syncytiotrophoblasts, extravillous trophoblasts, and other endogenous vascular cells), which were identified by immunofluorescence, flow cytometry analyses, real‐time quantitative reverse transcription polymerase chain reaction and single‐cell RNA‐seq. Moreover, the 3D tissue was able to secrete the placenta‐specific hormone human chorionic gonadotropin β (hCG‐β) and vascular endothelial growth factor A (VEGFA). The tissue responded to the inflammatory factor tumor necrosis factor‐α (TNF‐α) and VEGF receptor inhibitors. This new model system can represent the major features of placental cellular components, and function, which have not been realized in 2D monolayer cultures. The developed tissue system might open new avenues for studying normal early human placental development and its disease states. John Wiley & Sons, Inc. 2022-09-23 /pmc/articles/PMC9842056/ /pubmed/36684087 http://dx.doi.org/10.1002/btm2.10390 Text en © 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. 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 Research Articles
Cui, Kangli
Chen, Tingwei
Zhu, Yujuan
Shi, Yang
Guo, Yaqiong
Qin, Jianhua
Engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells
title Engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells
title_full Engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells
title_fullStr Engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells
title_full_unstemmed Engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells
title_short Engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells
title_sort engineering placenta‐like organoids containing endogenous vascular cells from human‐induced pluripotent stem cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842056/
https://www.ncbi.nlm.nih.gov/pubmed/36684087
http://dx.doi.org/10.1002/btm2.10390
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