| Literature DB >> 31626770 |
Ronghui Li1, Cuiqing Zhong1, Yang Yu2, Haisong Liu1, Masahiro Sakurai3, Leqian Yu4, Zheying Min5, Lei Shi6, Yulei Wei7, Yuta Takahashi1, Hsin-Kai Liao6, Jie Qiao5, Hongkui Deng8, Estrella Nuñez-Delicado9, Concepcion Rodriguez Esteban1, Jun Wu10, Juan Carlos Izpisua Belmonte11.
Abstract
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.Entities:
Keywords: EPS cells; EPS-blastoid; blastocyst; blastoids; extended pluripotent stem cells; implantation; reprogramming; totipotent
Mesh:
Year: 2019 PMID: 31626770 DOI: 10.1016/j.cell.2019.09.029
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582