Publications by authors named "Emilie Wildschutz"

The ability to study human post-implantation development remains limited owing to ethical and technical challenges associated with intrauterine development after implantation. Embryo-like models with spatially organized morphogenesis and structure of all defining embryonic and extra-embryonic tissues of the post-implantation human conceptus (that is, the embryonic disc, the bilaminar disc, the yolk sac, the chorionic sac and the surrounding trophoblast layer) remain lacking. Mouse naive embryonic stem cells have recently been shown to give rise to embryonic and extra-embryonic stem cells capable of self-assembling into post-gastrulation structured stem-cell-based embryo models with spatially organized morphogenesis (called SEMs).

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In vitro cultured stem cells with distinct developmental capacities can contribute to embryonic or extraembryonic tissues after microinjection into pre-implantation mammalian embryos. However, whether cultured stem cells can independently give rise to entire gastrulating embryo-like structures with embryonic and extraembryonic compartments remains unknown. Here, we adapt a recently established platform for prolonged ex utero growth of natural embryos to generate mouse post-gastrulation synthetic whole embryo models (sEmbryos), with both embryonic and extraembryonic compartments, starting solely from naive ESCs.

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Article Synopsis
  • This study focuses on isolating human pluripotent stem cells (PSCs) that exhibit naive pluripotency characteristics while retaining their ability to differentiate into different cell types and maintaining genetic integrity.* -
  • Researchers engineered systems to identify conditions that induce these naive PSC features, discovering that inhibiting certain pathways (WNT/β-CATENIN, PKC, and SRC) effectively promotes the formation of these stem cells, capable of developing into trophoblast and extraembryonic cells in lab settings.* -
  • The research highlights key differences in signaling required for naive pluripotency between humans and mice, and suggests that inhibiting NOTCH/RBPj can serve as an alternative to MEK/ERK inhibition,
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