Abstract
Development of the asymmetric amniotic sac - with the embryonic disc and amniotic ectoderm occupying opposite poles - is a vital milestone during human embryo implantation. Although essential to embryogenesis and pregnancy, amniotic sac development in humans remains poorly understood. Here, we report a human pluripotent stem cell (hPSC)-based model, termed the post-implantation amniotic sac embryoid (PASE), that recapitulates multiple post-implantation embryogenic events centered around amniotic sac development. Without maternal or extraembryonic tissues, the PASE self-organizes into an epithelial cyst with an asymmetric amniotic ectoderm-epiblast pattern that resembles the human amniotic sac. Upon further development, the PASE initiates a process that resembles posterior primitive streak development in a SNAI1-dependent manner. Furthermore, we observe asymmetric BMP-SMAD signaling concurrent with PASE development, and establish that BMP-SMAD activation/inhibition modulates stable PASE development. This study reveals a previously unrecognized fate potential of human pluripotent stem cells and provides a platform for advancing human embryology.
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CITATION STYLE
Shao, Y., Taniguchi, K., Townshend, R. F., Miki, T., Gumucio, D. L., & Fu, J. (2017). A pluripotent stem cell-based model for post-implantation human amniotic sac development. Nature Communications, 8(1). https://doi.org/10.1038/s41467-017-00236-w
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