Growth factor-mediated coupling between lineage size and cell fate choice underlies robustness of mammalian development Journal Article


Authors: Saiz, N.; Mora-Bitria, L.; Rahman, S.; George, H.; Herder, J. P.; García-Ojalvo, J.; Hadjantonakis, A. K.
Article Title: Growth factor-mediated coupling between lineage size and cell fate choice underlies robustness of mammalian development
Abstract: Precise control and maintenance of population size is fundamental for organismal development and homeostasis. The three cell types of the mammalian blastocyst are generated in precise proportions over a short time, suggesting a mechanism to ensure a reproducible outcome. We developed a minimal mathematical model demonstrating growth factor signaling is sufficient to guarantee this robustness and which anticipates an embryo's response to perturbations in lineage composition. Addition of lineage-restricted cells both in vivo and in silico, causes a shift of the fate of progenitors away from the supernumerary cell type, while eliminating cells using laser ablation biases the specification of progenitors towards the targeted cell type. Finally, FGF4 couples fate decisions to lineage composition through changes in local growth factor concentration, providing a basis for the regulative abilities of the early mammalian embryo whereby fate decisions are coordinated at the population level to robustly generate tissues in the right proportions. © 2020, eLife Sciences Publications Ltd. All rights reserved.
Journal Title: eLife
Volume: 9
ISSN: 2050-084X
Publisher: eLife Sciences Publications Ltd.  
Date Published: 2020-07-28
Start Page: e56079
Language: English
DOI: 10.7554/eLife.56079
PUBMED: 32720894
PROVIDER: scopus
PMCID: PMC7513828
DOI/URL:
Notes: Article -- Export Date: 1 October 2020 -- Source: Scopus
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  1. Shahadat Rahman
    2 Rahman
  2. Jeremy Herder
    1 Herder
  3. Hannah George
    1 George