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Gastrulation establishes the three primary tissues of an embryo: the ectoderm, mesoderm, and endoderm. This developmental process relies on a series of intricate cellular movements, which in humans transforms a flat, “bilaminar disc” composed of two cell sheets into a three-tiered structure. In the resulting embryo, the endoderm serves as the bottom layer, and stacked directly above it is the intermediate mesoderm, and then the uppermost ectoderm. Respectively, these tissue strata...
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The development of all multicellular organisms starts with the fusion of haploid cells called sperm and egg to form a diploid zygote. A zygote is a totipotent cell that can develop into a complete organism. The zygote undergoes cell division or cleavage to form an 8-cell mass. Until this stage, the cells are spherical, loosely attached, and remain totipotent. Totipotent cells are capable of developing both the embryonic and the extraembryonic tissues. However, as they continue to divide, they...
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Active morphogenesis of patterned epithelial shells.

Diana Khoromskaia1, Guillaume Salbreux1,2

  • 1The Francis Crick Institute, London, United Kingdom.

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|January 17, 2023
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Summary
This summary is machine-generated.

Epithelial tissue shape changes during development arise from internal cell forces. This study models tissues as active viscoelastic surfaces, revealing how tension and bending forces drive morphogenesis, forming structures like folds and buds.

Keywords:
active matterdeforming surfacefluid dynamicsmorphogenesisnematic order parameternonephysics of living systemstissue mechanics

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Area of Science:

  • Biophysics
  • Developmental Biology
  • Cellular Mechanics

Background:

  • Epithelial tissue morphogenesis is vital for embryonic development and organoid formation.
  • Cellular cytoskeleton generates active forces driving tissue shape transformations.
  • The relationship between local forces, tissue geometry, and macroscopic morphogenesis is not fully understood.

Purpose of the Study:

  • To model epithelial sheets as active viscoelastic surfaces to understand tissue-scale morphogenesis.
  • To investigate how patterned internal tensions, bending moments, and nematic alignment influence tissue deformation.
  • To identify the mechanical principles underlying fundamental morphogenetic processes.

Main Methods:

  • Developed a theoretical framework describing epithelial sheets as active viscoelastic surfaces.
  • Incorporated isotropic and nematic (in-plane alignment) effects on active tensions and bending moments.
  • Analyzed deformation of closed shells under patterned internal forces and moments, presenting phase diagrams and exploring dynamics.

Main Results:

  • Demonstrated that nematic alignment combined with gradients in tension and bending moments can induce anisotropic active stresses.
  • Identified specific combinations of forces and moments sufficient to generate key morphogenetic events.
  • Phase diagrams revealed distinct mechanical equilibrium shapes and dynamic deformation pathways.

Conclusions:

  • A combination of nematic alignment and gradients in internal tensions and bending moments is sufficient to drive epithelial morphogenesis.
  • The model successfully reproduces fundamental morphogenetic building blocks, including folding, budding, flattening, and tubulation.
  • Provides a mechanical framework for understanding how active cellular forces translate into tissue-scale shape changes.