@article{eb9b46d44bd34132ac08ce282002fe11,
title = "An in vitro model of early anteroposterior organization during human development",
abstract = "The body plan of the mammalian embryo is shaped through the process of gastrulation, an early developmental event that transforms an isotropic group of cells into an ensemble of tissues that is ordered with reference to three orthogonal axes1. Although model organisms have provided much insight into this process, we know very little about gastrulation in humans, owing to the difficulty of obtaining embryos at such early stages of development and the ethical and technical restrictions that limit the feasibility of observing gastrulation ex vivo2. Here we show that human embryonic stem cells can be used to generate gastruloids-three-dimensional multicellular aggregates that differentiate to form derivatives of the three germ layers organized spatiotemporally, without additional extra-embryonic tissues. Human gastruloids undergo elongation along an anteroposterior axis, and we use spatial transcriptomics to show that they exhibit patterned gene expression. This includes a signature of somitogenesis that suggests that 72-h human gastruloids show some features of Carnegie-stage-9 embryos3. Our study represents an experimentally tractable model system to reveal and examine human-specific regulatory processes that occur during axial organization in early development.",
keywords = "Body Patterning/genetics, Gastrula/cytology, Gene Expression Regulation, Developmental, Human Embryonic Stem Cells/cytology, Humans, In Vitro Techniques, Organoids/cytology, Signal Transduction, Somites/cytology, Transcriptome",
author = "Naomi Moris and Kerim Anlas and {van den Brink}, {Susanne C} and Anna Alemany and Julia Schr{\"o}der and Sabitri Ghimire and Tina Balayo and {van Oudenaarden}, Alexander and {Martinez Arias}, Alfonso",
note = "Funding Information: Acknowledgements We thank V. Trivedi for his help writing the dynamic fluorescent reporter analysis code; D. Turner and A. Baranowski for their help developing the image analysis code; K. Muller from the Cambridge Advance Imaging Centre (CAIC) for help with scanning electron microscopy; the Utrecht Sequencing Facility for sequencing; A. Ebbing, J. Vivi{\'e} and M. Betist for the robotized tomo-seq protocol; and members of the Martinez Arias and van Oudenaarden laboratories, as well as B. Steventon, P. Rugg-Gunn, M. L{\"u}tolf, M. Johnson and N. Hopwood, for discussions over the course of this work. This work was supported by funds from the Newton Trust (INT16.24b), Leverhulme Trust (RPG-2018-356) and MRC (MR/R017190/1) to A.M.A., N.M., S.G. and T.B. and a European Research Council Advanced Grant (ERC-AdG 742225-IntScOmics), a Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO) TOP award (NWO-CW 714.016.001) and the Foundation for Fundamental Research on Matter, financially supported by NWO (FOM-14NOISE01), to S.C.v.d.B., A.A. and A.v.O. This work is part of the Oncode Institute, which is partly financed by the Dutch Cancer Society. It was also supported by a Constance Work Junior Research Fellowship from Newnham College, Cambridge to N.M. and an Erasmus+ grant to K.A. and J.S. Publisher Copyright: {\textcopyright} 2020, The Author(s), under exclusive licence to Springer Nature Limited. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.",
year = "2020",
month = jun,
day = "18",
doi = "10.1038/s41586-020-2383-9",
language = "English",
volume = "582",
pages = "410--415",
journal = "Nature",
issn = "0028-0836",
publisher = "Nature Publishing Group",
number = "7812",
}