Self-renewing human naïve pluripotent stem cells dedifferentiate in 3D culture and form blastoids spontaneously

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作者
Mingyue Guo
Jinyi Wu
Chuanxin Chen
Xinggu Wang
An Gong
Wei Guan
Rowan M. Karvas
Kexin Wang
Mingwei Min
Yixuan Wang
Thorold W. Theunissen
Shaorong Gao
José C. R. Silva
机构
[1] Guangzhou Medical University,Department of Developmental Biology and Center of Regenerative Medicine
[2] Guangzhou National Laboratory,Shanghai Key Laboratory of Maternal and Fetal Medicine, Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, School of Life Sciences and Technology
[3] Guangzhou International Bio Island,undefined
[4] Bioland Laboratory,undefined
[5] Guangzhou International Bio Island,undefined
[6] The Fifth Affiliated Hospital of Guangzhou Medical University,undefined
[7] Washington University School of Medicine,undefined
[8] Tongji University,undefined
来源
Nature Communications | / 15卷
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摘要
Human naïve pluripotent stem cells (hnPSCs) can generate integrated models of blastocysts termed blastoids upon switch to inductive medium. However, the underlying mechanisms remain obscure. Here we report that self-renewing hnPSCs spontaneously and efficiently give rise to blastoids upon three dimensional (3D) suspension culture. The spontaneous blastoids mimic early stage human blastocysts in terms of structure, size, and transcriptome characteristics and are capable of progressing to post-implantation stages. This property is conferred by the glycogen synthase kinase-3 (GSK3) signalling inhibitor IM-12 present in 5iLAF self-renewing medium. IM-12 upregulates oxidative phosphorylation-associated genes that underly the capacity of hnPSCs to generate blastoids spontaneously. Starting from day one of self-organization, hnPSCs at the boundary of all 3D aggregates dedifferentiate into E5 embryo-like intermediates. Intermediates co-express SOX2/OCT4 and GATA6 and by day 3 specify trophoblast fate, which coincides with cavity and blastoid formation. In summary, spontaneous blastoid formation results from 3D culture triggering dedifferentiation of hnPSCs into earlier embryo-like intermediates which are then competent to segregate blastocyst fates.
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