2021
DOI: 10.1038/s41580-020-00318-6
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Programmed and self-organized flow of information during morphogenesis

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Cited by 229 publications
(199 citation statements)
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“…The original approach to investigate cellular population dynamics has mainly been deterministic, i.e., a stable genetic code defines cell fate as a programmed hierarchical process. More recently, research has shown how another group of mechanisms based on stochastic self-organisation plays a complementary role in morphogenesis (i.e., organ development) and cell development [ 41 ]. Under this perspective, genetic factors would interact with self-organisation mechanisms to balance the growth of an organism and the organisation of cellular assemblies in direct connection with environmental factors.…”
Section: Discussionmentioning
confidence: 99%
“…The original approach to investigate cellular population dynamics has mainly been deterministic, i.e., a stable genetic code defines cell fate as a programmed hierarchical process. More recently, research has shown how another group of mechanisms based on stochastic self-organisation plays a complementary role in morphogenesis (i.e., organ development) and cell development [ 41 ]. Under this perspective, genetic factors would interact with self-organisation mechanisms to balance the growth of an organism and the organisation of cellular assemblies in direct connection with environmental factors.…”
Section: Discussionmentioning
confidence: 99%
“…Most of the current work in the mechanobiology field is devoted to the understanding of how forces drive the arrangement of cells in space such as cell intercalation, cell migration, or collective cell migration during self-organization and spreading of tissues. From those studies we know how forces produced by oriented cell division and growth, directed cell crawling or bending of cell sheets, integrate local cell shape changes (for reviews see Heisenberg and Bellaïche, 2013 ; Collinet and Lecuit, 2021 ). However, how such mechanical forces influence cell fate is still an open question.…”
Section: Cell and Tissue Mechanics During Embryonic Developmentmentioning
confidence: 99%
“…As the stiffness of ECM is sometimes attributed to the abundance of collagen [123], which can be realistically modeled as a viscoelastic material with quantifiable storage and loss moduli [124], cell-matrix interactions and resulting cell migration thus exhibit dynamic time-dependent mechanical responses [105]. Paths of migration and areas that cells migrate toward are likely of different viscosity in addition to higher elasticity, thereby impacting the timescale of the responses of migrating cells to stiffness gradients [125]. To elucidate the effect of ECM viscosity on cell movements, several in vitro studies have either isolated the effects of the viscosity of substrates or implemented tunable storage-to-loss moduli ratios of substrates.…”
Section: Durotaxis and Viscotaxismentioning
confidence: 99%