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Gastruloid-derived primordial germ cell-like cells develop dynamically within integrated tissues.

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Abstract

Primordial germ cells (PGCs) are the early embryonic precursors of gametes - sperm and egg cells. PGC-like cells (PGCLCs) can currently be derived in vitro from pluripotent cells exposed to signalling cocktails and aggregated into large embryonic bodies, but these do not recapitulate the native embryonic environment during PGC formation. Here, we show that mouse gastruloids, a three-dimensional in vitro model of gastrulation, contain a population of gastruloid-derived PGCLCs (Gld-PGCLCs) that resemble early PGCs in vivo. Importantly, the conserved organisation of mouse gastruloids leads to coordinated spatial and temporal localisation of Gld-PGCLCs relative to surrounding somatic cells, even in the absence of specific exogenous PGC-specific signalling or extra-embryonic tissues. In gastruloids, self-organised interactions between cells and tissues, including the endodermal epithelium, enables the specification and subsequent maturation of a pool of Gld-PGCLCs. As such, mouse gastruloids represent a new source of PGCLCs in vitro and, owing to their inherent co-development, serve as a novel model to study the dynamics of PGC development within integrated tissue environments.

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Peer reviewed: True


Acknowledgements: We would like to thank Azim Surani, Mitinori Saitou, Christian Schroeter and Tristan Rodriquez for kindly providing cell lines used in this manuscript. We also thank Alfonso Martinez Arias for his support, advice and feedback throughout this project, as well as Federica Cermola for feedback on preliminary experiments, Carla Mulas and Ken Jones for their advice and expertise in CRISPR/Cas9 gene editing, and Ignacio Rodriquez Polo for feedback on the manuscript. In addition, the authors gratefully acknowledge the Francis Crick Light Microscopy, Flow Cytometry, Advanced Sequencing and Bioinformatics and Biostatistics Science and Technology Platforms (STPs) for their support and assistance in this work.


Funder: Francis Crick Institute; doi: http://dx.doi.org/10.13039/100010438

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Journal ISSN

0950-1991
1477-9129

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150

Publisher

The Company of Biologists

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Except where otherwised noted, this item's license is described as http://creativecommons.org/licenses/by/4.0
Sponsorship
Wellcome Trust (105031/D/14/Z)

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