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Cell fate clusters in ICM organoids arise from cell fate heredity and division: a modelling approach.
Liebisch, Tim; Drusko, Armin; Mathew, Biena; Stelzer, Ernst H K; Fischer, Sabine C; Matthäus, Franziska.
Afiliação
  • Liebisch T; Faculty of Biological Sciences and Frankfurt Institute for Advanced Studies (FIAS), Goethe Universität Frankfurt am Main, Ruth-Moufang-Straße 1, 60438, Frankfurt, Germany. liebisch@fias.uni-frankfurt.de.
  • Drusko A; Faculty of Biological Sciences and Frankfurt Institute for Advanced Studies (FIAS), Goethe Universität Frankfurt am Main, Ruth-Moufang-Straße 1, 60438, Frankfurt, Germany.
  • Mathew B; Faculty of Biological Sciences and Buchmann Institute for Molecular Life Sciences (BMLS), Goethe Universität Frankfurt am Main, Max-von-Laue Str. 15, 60438, Frankfurt, Germany.
  • Stelzer EHK; Faculty of Biological Sciences and Buchmann Institute for Molecular Life Sciences (BMLS), Goethe Universität Frankfurt am Main, Max-von-Laue Str. 15, 60438, Frankfurt, Germany.
  • Fischer SC; Center for Computational and Theoretical Biology (CCTB), Julius-Maximilians-Universität Würzburg, Campus Hubland Nord 32, 97074, Würzburg, Germany.
  • Matthäus F; Faculty of Biological Sciences and Frankfurt Institute for Advanced Studies (FIAS), Goethe Universität Frankfurt am Main, Ruth-Moufang-Straße 1, 60438, Frankfurt, Germany.
Sci Rep ; 10(1): 22405, 2020 12 29.
Article em En | MEDLINE | ID: mdl-33376253
During the mammalian preimplantation phase, cells undergo two subsequent cell fate decisions. During the first decision, the trophectoderm and the inner cell mass are formed. Subsequently, the inner cell mass segregates into the epiblast and the primitive endoderm. Inner cell mass organoids represent an experimental model system, mimicking the second cell fate decision. It has been shown that cells of the same fate tend to cluster stronger than expected for random cell fate decisions. Three major processes are hypothesised to contribute to the cell fate arrangements: (1) chemical signalling; (2) cell sorting; and (3) cell proliferation. In order to quantify the influence of cell proliferation on the observed cell lineage type clustering, we developed an agent-based model accounting for mechanical cell-cell interaction, i.e. adhesion and repulsion, cell division, stochastic cell fate decision and cell fate heredity. The model supports the hypothesis that initial cell fate acquisition is a stochastically driven process, taking place in the early development of inner cell mass organoids. Further, we show that the observed neighbourhood structures can emerge solely due to cell fate heredity during cell division.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Organoides / Diferenciação Celular / Divisão Celular / Linhagem da Célula / Células-Tronco Embrionárias Murinas / Modelos Biológicos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Sci Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Organoides / Diferenciação Celular / Divisão Celular / Linhagem da Célula / Células-Tronco Embrionárias Murinas / Modelos Biológicos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Sci Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha