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Multi-axial self-organization properties of mouse embryonic stem cells into gastruloids

Author

Listed:
  • Leonardo Beccari

    (University of Geneva)

  • Naomi Moris

    (University of Cambridge)

  • Mehmet Girgin

    (Federal Institute of Technology EPFL)

  • David A. Turner

    (University of Cambridge)

  • Peter Baillie-Johnson

    (University of Cambridge
    University of Cambridge)

  • Anne-Catherine Cossy

    (School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL))

  • Matthias P. Lutolf

    (Federal Institute of Technology EPFL)

  • Denis Duboule

    (University of Geneva
    School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL))

  • Alfonso Martinez Arias

    (University of Cambridge)

Abstract

The emergence of multiple axes is an essential element in the establishment of the mammalian body plan. This process takes place shortly after implantation of the embryo within the uterus and relies on the activity of gene regulatory networks that coordinate transcription in space and time. Whereas genetic approaches have revealed important aspects of these processes1, a mechanistic understanding is hampered by the poor experimental accessibility of early post-implantation stages. Here we show that small aggregates of mouse embryonic stem cells (ESCs), when stimulated to undergo gastrulation-like events and elongation in vitro, can organize a post-occipital pattern of neural, mesodermal and endodermal derivatives that mimic embryonic spatial and temporal gene expression. The establishment of the three major body axes in these ‘gastruloids’2,3 suggests that the mechanisms involved are interdependent. Specifically, gastruloids display the hallmarks of axial gene regulatory systems as exemplified by the implementation of collinear Hox transcriptional patterns along an extending antero-posterior axis. These results reveal an unanticipated self-organizing capacity of aggregated ESCs and suggest that gastruloids could be used as a complementary system to study early developmental events in the mammalian embryo.

Suggested Citation

  • Leonardo Beccari & Naomi Moris & Mehmet Girgin & David A. Turner & Peter Baillie-Johnson & Anne-Catherine Cossy & Matthias P. Lutolf & Denis Duboule & Alfonso Martinez Arias, 2018. "Multi-axial self-organization properties of mouse embryonic stem cells into gastruloids," Nature, Nature, vol. 562(7726), pages 272-276, October.
  • Handle: RePEc:nat:nature:v:562:y:2018:i:7726:d:10.1038_s41586-018-0578-0
    DOI: 10.1038/s41586-018-0578-0
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    Cited by:

    1. Ana Sousa-Ortega & Javier Vázquez-Marín & Estefanía Sanabria-Reinoso & Jorge Corbacho & Rocío Polvillo & Alejandro Campoy-López & Lorena Buono & Felix Loosli & María Almuedo-Castillo & Juan R. Martíne, 2023. "A Yap-dependent mechanoregulatory program sustains cell migration for embryo axis assembly," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    2. Marina Sanaki-Matsumiya & Mitsuhiro Matsuda & Nicola Gritti & Fumio Nakaki & James Sharpe & Vikas Trivedi & Miki Ebisuya, 2022. "Periodic formation of epithelial somites from human pluripotent stem cells," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    3. Sandhya Malla & Kanchan Kumari & Carlos A. García-Prieto & Jonatan Caroli & Anna Nordin & Trinh T. T. Phan & Devi Prasad Bhattarai & Carlos Martinez-Gamero & Eshagh Dorafshan & Stephanie Stransky & Da, 2024. "The scaffolding function of LSD1 controls DNA methylation in mouse ESCs," Nature Communications, Nature, vol. 15(1), pages 1-24, December.
    4. Chet H. Loh & Siebe Genesen & Matteo Perino & Magnus R. Bark & Gert Jan C. Veenstra, 2021. "Loss of PRC2 subunits primes lineage choice during exit of pluripotency," Nature Communications, Nature, vol. 12(1), pages 1-14, December.

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