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Trinish Sarkar1, Victor Yashunsky1,2, Louis Brézin1,3

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Scientists discovered a new way muscle cells form perpendicular layers in vitro. Extracellular matrix (ECM) at stationary defects guides cell organization, creating crisscross muscle bilayers essential for hydrostatic skeletons.

Keywords:
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Area of Science:

  • Cell biology
  • Biophysics
  • Developmental biology

Background:

  • Hydrostatic skeletons rely on perpendicularly oriented muscle cell layers.
  • In vivo, muscle bilayers assemble and develop with a specific crisscross orientation.

Purpose of the Study:

  • To identify an alternative mechanism for crisscross bilayering of myoblasts in vitro.
  • To understand the role of extracellular matrix (ECM) in this process.

Main Methods:

  • Describing myoblast sheets as contractile active nematics.
  • Observing topological defects and their self-propulsion.
  • Analyzing cell behavior around stationary defects and ECM production.

Main Results:

  • Myoblast sheets exhibit nematic order with self-propelling topological defects.
  • Extracellular matrix (ECM) production leads to a subpopulation of stationary defects.
  • Perpendicular bilayering occurs at these stationary defects, mediated by ECM secretion.

Conclusions:

  • A novel in vitro mechanism for crisscross muscle bilayer formation was identified.
  • Stationary topological defects, influenced by ECM, orchestrate cell migration and organization.
  • This process provides insights into the development of hydrostatic skeletons.