生物
胚泡
胚胎干细胞
内细胞团
细胞生物学
重编程
卵裂球
胚胎
电池类型
胚胎发生
干细胞
蜕膜化
细胞
免疫学
遗传学
基因
作者
Ronghui Li,Cuiqing Zhong,Yang Yu,Haisong Liu,Masahiro Sakurai,Leqian Yu,Zheying Min,Lei Shi,Yulei Wei,Yuta Takahashi,Hsin-Kai Liao,Jie Qiao,Hongkui Deng,Estrella Núñez‐Delicado,Concepción Rodrı́guez Esteban,Jun Wu,Juan Carlos Izpisúa Belmonte
出处
期刊:Cell
[Cell Press]
日期:2019-10-01
卷期号:179 (3): 687-702.e18
被引量:236
标识
DOI:10.1016/j.cell.2019.09.029
摘要
A single mouse blastomere from an embryo until the 8-cell stage can generate an entire blastocyst. Whether laboratory-cultured cells retain a similar generative capacity remains unknown. Starting from a single stem cell type, extended pluripotent stem (EPS) cells, we established a 3D differentiation system that enabled the generation of blastocyst-like structures (EPS-blastoids) through lineage segregation and self-organization. EPS-blastoids resembled blastocysts in morphology and cell-lineage allocation and recapitulated key morphogenetic events during preimplantation and early postimplantation development in vitro. Upon transfer, some EPS-blastoids underwent implantation, induced decidualization, and generated live, albeit disorganized, tissues in utero. Single-cell and bulk RNA-sequencing analysis revealed that EPS-blastoids contained all three blastocyst cell lineages and shared transcriptional similarity with natural blastocysts. We also provide proof of concept that EPS-blastoids can be generated from adult cells via cellular reprogramming. EPS-blastoids provide a unique platform for studying early embryogenesis and pave the way to creating viable synthetic embryos by using cultured cells.
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