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Baffled‐flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function

Human embryonic stem cells (hESCs) have become an ideal cell source for the ex vivo generation of megakaryocyte (MK) and platelet products for clinical applications. However, an ongoing challenge is to establish scalable culture systems to maximize the yield of stem cell‐derived MKs that release pla...

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Autores principales: Wu, Xumin, Zhang, Bowen, Chen, Keyi, Zhao, Jiahui, Li, Yunxing, Li, Jisheng, Liu, Chuanli, He, Lijuan, Fan, Tao, Wang, Chao, Li, Yan, Pei, Xuetao, Li, Yanhua
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/PMC10693187/
https://www.ncbi.nlm.nih.gov/pubmed/37088551
http://dx.doi.org/10.1111/cpr.13484
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author Wu, Xumin
Zhang, Bowen
Chen, Keyi
Zhao, Jiahui
Li, Yunxing
Li, Jisheng
Liu, Chuanli
He, Lijuan
Fan, Tao
Wang, Chao
Li, Yan
Pei, Xuetao
Li, Yanhua
author_facet Wu, Xumin
Zhang, Bowen
Chen, Keyi
Zhao, Jiahui
Li, Yunxing
Li, Jisheng
Liu, Chuanli
He, Lijuan
Fan, Tao
Wang, Chao
Li, Yan
Pei, Xuetao
Li, Yanhua
author_sort Wu, Xumin
collection PubMed
description Human embryonic stem cells (hESCs) have become an ideal cell source for the ex vivo generation of megakaryocyte (MK) and platelet products for clinical applications. However, an ongoing challenge is to establish scalable culture systems to maximize the yield of stem cell‐derived MKs that release platelets. We defined a specific dynamic 3D manufacturing system in a baffled‐flow manner that could remarkably facilitate megakaryopoiesis and increase the yield of platelet‐producing MKs from hESCs within a 12‐day induction period. Additionally, an increased number of >16N ploidy MKs, proplatelets, and platelets were generated from induced cells harvested on Day 12 using the specific dynamic culture method. The specific dynamic culture method significantly enhanced endothelium‐to‐haematopoietic transition and early haematopoiesis. More importantly, MK fate was significantly facilitated in a specific dynamic manner during early haematopoiesis. Mechanistically, this dynamic culture significantly enhanced mitochondrial function via the oxidative phosphorylation pathway and caused differentiation skewing of hESCs toward megakaryopoiesis. This study can aid in the automatic and scalable production of MKs from stem cells using baffled‐flow bioreactors and assist in the manufacturing of hESC‐derived MK and platelet products.
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spelling pubmed-106931872023-12-03 Baffled‐flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function Wu, Xumin Zhang, Bowen Chen, Keyi Zhao, Jiahui Li, Yunxing Li, Jisheng Liu, Chuanli He, Lijuan Fan, Tao Wang, Chao Li, Yan Pei, Xuetao Li, Yanhua Cell Prolif Original Articles Human embryonic stem cells (hESCs) have become an ideal cell source for the ex vivo generation of megakaryocyte (MK) and platelet products for clinical applications. However, an ongoing challenge is to establish scalable culture systems to maximize the yield of stem cell‐derived MKs that release platelets. We defined a specific dynamic 3D manufacturing system in a baffled‐flow manner that could remarkably facilitate megakaryopoiesis and increase the yield of platelet‐producing MKs from hESCs within a 12‐day induction period. Additionally, an increased number of >16N ploidy MKs, proplatelets, and platelets were generated from induced cells harvested on Day 12 using the specific dynamic culture method. The specific dynamic culture method significantly enhanced endothelium‐to‐haematopoietic transition and early haematopoiesis. More importantly, MK fate was significantly facilitated in a specific dynamic manner during early haematopoiesis. Mechanistically, this dynamic culture significantly enhanced mitochondrial function via the oxidative phosphorylation pathway and caused differentiation skewing of hESCs toward megakaryopoiesis. This study can aid in the automatic and scalable production of MKs from stem cells using baffled‐flow bioreactors and assist in the manufacturing of hESC‐derived MK and platelet products. John Wiley and Sons Inc. 2023-04-23 /pmc/articles/PMC10693187/ /pubmed/37088551 http://dx.doi.org/10.1111/cpr.13484 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
Wu, Xumin
Zhang, Bowen
Chen, Keyi
Zhao, Jiahui
Li, Yunxing
Li, Jisheng
Liu, Chuanli
He, Lijuan
Fan, Tao
Wang, Chao
Li, Yan
Pei, Xuetao
Li, Yanhua
Baffled‐flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function
title Baffled‐flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function
title_full Baffled‐flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function
title_fullStr Baffled‐flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function
title_full_unstemmed Baffled‐flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function
title_short Baffled‐flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function
title_sort baffled‐flow culture system enables the mass production of megakaryocytes from human embryonic stem cells by enhancing mitochondrial function
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693187/
https://www.ncbi.nlm.nih.gov/pubmed/37088551
http://dx.doi.org/10.1111/cpr.13484
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