Assembly of complete mouse embryo models from embryonic and induced stem cell types in vitro

The interaction between embryonic and extraembryonic tissues is critical in natural mouse embryogenesis. Here, to enable such interaction in vitro, we describe a protocol to assemble a complete mouse embryo model using mouse embryonic stem cells and induced embryonic stem cells to express Cdx2 (or trophoblast stem cells) and Gata4 to reconstitute the epiblast, extraembryonic ectoderm and visceral endoderm lineages, respectively. The resulting complete embryo models recapitulate development from embryonic day 5.0 to 8.5, generating advanced embryonic and extraembryonic tissues that develop through gastrulation to initiate organogenesis to form a head and a beating heart structure as well as a yolk sac and chorion. Once the required stem cell lines are stably maintained in culture, the protocol requires 1 day to assemble complete embryo models and a further 8 days to culture them until headfold stages, although structures can be collected at earlier developmental stages as required. This protocol can be easily performed by researchers with experience in mouse stem cell culture, although they will benefit from knowledge of natural mouse embryos at early postimplantation stages.

Automated summary

This protocol uses mouse embryonic stem cells and induced embryonic stem cells to express specific genes, and reconstructs the lineages of embryonic and extraembryonic tissues to assemble a complete mouse embryo model. This model can recapitulate the process of embryonic development and generate advanced embryonic and extraembryonic tissues, forming structures such as the head and heart. This protocol requires 9 days and requires researchers to have experience in mouse stem cell culture and an understanding of natural mouse embryos.