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Discrete Mesh Approach in Morphogenesis Modelling: the Example of Gastrulation
J Demongeot1, A Lontos2, E Promayon2
1AGIM, Faculty of Medicine of Grenoble, University J. Fourier, 38700, La Tronche, France. Jacques.Demongeot@agim.eu.
Acta Biotheoretica
|November 18, 2016
Summary
The shape of the Drosophila melanogaster embryo drives ventral furrow invagination during early embryogenesis. This biomechanical model explains how cell constriction initiates this key developmental process.
Area of Science:
- Developmental Biology
- Biophysics
- Computational Biology
Background:
- Morphogenesis involves processes generating tissue shapes and cellular organization.
- Gastrulation, a key embryonic process, involves significant tissue remodeling.
- Understanding early embryogenesis requires robust modeling of cellular behaviors.
Purpose of the Study:
- To investigate the link between apical constriction and ventral furrow invagination initiation.
- To model the early stages of Drosophila melanogaster embryogenesis using a biomechanical approach.
- To explore the role of embryo geometry in morphogenesis.
Main Methods:
- Developed a 3D biomechanical model of the Drosophila melanogaster embryo.
- Utilized the finite element method for simulations.
- Modeled cells as elastic hexahedron contours with attached neighbors, applying contractile forces.
Main Results:
- Invagination initiates at the ventral curved extremities and propagates medially.
- The 'pill-shaped' geometry of the embryo is identified as a key factor in directing invagination.
- Simulations with spherical geometry (Xenopus laevis) show different invagination patterns.
Conclusions:
- The specific shape of the Drosophila melanogaster embryo uniquely drives ventral furrow invagination.
- Apical constriction and embryo geometry are critical for initiating gastrulation.
- Further research will explore the impact of cell proliferation on furrow closure.
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