Microgel culture and spatial identity mapping elucidate the signalling requirements for primate epiblast and amnion formation

Clara Munger(Wellcome/MRC Cambridge Stem Cell Institute), Timo N. Kohler(Wellcome/MRC Cambridge Stem Cell Institute), Erin Slatery(Wellcome/MRC Cambridge Stem Cell Institute), Anna L. Ellermann(University of Cambridge), Sophie Bergmann(Wellcome/MRC Cambridge Stem Cell Institute), Christopher A. Penfold(Wellcome/MRC Cambridge Stem Cell Institute), Ioakeim Ampartzidis(Wellcome/MRC Cambridge Stem Cell Institute), Yutong Chen(Wellcome/MRC Cambridge Stem Cell Institute), Florian Hollfelder(University of Cambridge), Thorsten Boroviak(Wellcome/MRC Cambridge Stem Cell Institute)
Development
July 28, 2022
Cited by 18Open Access
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Abstract

The early specification and rapid growth of extraembryonic membranes are distinctive hallmarks of primate embryogenesis. These complex tasks are resolved through an intricate combination of signals controlling the induction of extraembryonic lineages and, at the same time, safeguarding the pluripotent epiblast. Here, we delineate the signals orchestrating primate epiblast and amnion identity. We encapsulated marmoset pluripotent stem cells into agarose microgels and identified culture conditions for the development of epiblast- and amnion-spheroids. Spatial identity mapping authenticated spheroids generated in vitro by comparison with marmoset embryos in vivo. We leveraged the microgel system to functionally interrogate the signalling environment of the post-implantation primate embryo. Single-cell profiling of the resulting spheroids demonstrated that activin/nodal signalling is required for embryonic lineage identity. BMP4 promoted amnion formation and maturation, which was counteracted by FGF signalling. Our combination of microgel culture, single-cell profiling and spatial identity mapping provides a powerful approach to decipher the essential cues for embryonic and extraembryonic lineage formation in primate embryogenesis.


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