Bilineage embryo-like structure from EPS cells can produce live mice with tetraploid trophectoderm

Author:

Liu Kuisheng1,Xu Xiaocui1,Bai Dandan1,Li Yanhe1,Zhang Yalin1,Jia Yanping1,Guo Mingyue1,Han Xiaoxiao1,Liu Yingdong1,Sheng Yifan1,Kou Xiaochen1,Zhao Yanhong1,Yin Jiqing1,Liu Sheng1,Chen Jiayu1,Wang Hong1,Wang Yixuan12,Liu Wenqiang1,Gao Shaorong12ORCID

Affiliation:

1. Shanghai Key Laboratory of Maternal Fetal Medicine, Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University , Shanghai, China

2. Translational Medical Center for Stem Cell Therapy and Institute for Regenerative Medicine, Shanghai East Hospital, School of Life Sciences and Technology, Tongji University , Shanghai, China

Abstract

Abstract Self-organized blastoids from extended pluripotent stem (EPS) cells possess enormous potential for investigating postimplantation embryo development and related diseases. However, the limited ability of postimplantation development of EPS-blastoids hinders its further application. In this study, single-cell transcriptomic analysis indicated that the “trophectoderm (TE)-like structure” of EPS-blastoids was primarily composed of primitive endoderm (PrE)-related cells instead of TE-related cells. We further identified PrE-like cells in EPS cell culture that contribute to the blastoid formation with TE-like structure. Inhibition of PrE cell differentiation by inhibiting MEK signaling or knockout of Gata6 in EPS cells markedly suppressed EPS-blastoid formation. Furthermore, we demonstrated that blastocyst-like structures reconstituted by combining the EPS-derived bilineage embryo-like structure (BLES) with either tetraploid embryos or tetraploid TE cells could implant normally and develop into live fetuses. In summary, our study reveals that TE improvement is critical for constructing a functional embryo using stem cells in vitro.

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Drug Discovery,Biochemistry,Biotechnology

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