Cellular Mechanisms of Embryonic Morphogenesis in C. elegans

Summary

Embryonic morphogenesis in Caenorhabditis elegans is orchestrated through tightly regulated cell shape changes, intercellular adhesion dynamics and cytoskeletal remodelling. During elongation, epidermal cells generate anisotropic contractile forces via actomyosin networks in coordination with underlying muscle tension transmitted through specialised junctions. Spatial patterning of cortical tension and stiffness guides directional tissue deformation along the antero-posterior axis. Concurrently, junctional complexes assemble and disassemble to permit cell rearrangements, while microtubule arrays facilitate targeted delivery of adhesion and remodelling factors. Underlying these mechanical events are conserved signalling modules, notably Rho GTPase pathways, that integrate biochemical cues with force generation to sculpt the embryo into its characteristic vermiform shape.

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Cellular Mechanisms of Embryonic Morphogenesis in C. elegans publication trend

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Technical terms

Actomyosin: A complex of actin filaments and myosin motors that contracts to generate cellular tension.

Cortical tension: The contractile force within the thin actin network beneath the plasma membrane that influences cell shape.

Hemidesmosomes: Adhesive structures that anchor epidermal cells to the underlying basement membrane and transmit tensile forces.

Adherens junctions: Cell–cell adhesion complexes that link the actin cytoskeletons of neighbouring cells, facilitating coordinated movement and shape change.

Microtubules: Rigid cytoskeletal filaments composed of tubulin, involved in intracellular transport and organisation of cellular architecture.

References

  1. The interplay of stiffness and force anisotropies drives embryo elongation. eLife (2017).
  2. Non-centrosomal epidermal microtubules act in parallel to LET-502/ROCK to promote C. elegans elongation. Development (2015).
  3. HMP-1/α-catenin promotes junctional mechanical integrity during morphogenesis. PLOS ONE (2018).

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