collaborateurs

Quentin Vagne

Maître-assistant(e) chez Physique de la biologie

  • T: +41 22 379 67 56
  • office 3004a (Sciences III)

  • Generic theory of interacting, spinning, active polar particles: A model for cell aggregates. Phys Rev E 2025 Jan;111(1-1):014423. 10.1103/PhysRevE.111.014423.

    résumé

    We present a generic framework for describing interacting, spinning, active polar particles, aimed at modeling dense cell aggregates, where cells are treated as polar, rotating objects that interact mechanically with one another and their surrounding environment. Using principles from nonequilibrium thermodynamics, we derive constitutive equations for interaction forces, torques, and polarity dynamics. We subsequently use this framework to analyze the spontaneous motion of cell doublets, uncovering a rich phase diagram of collective behaviors, including steady rotation driven by flow-polarity coupling or interactions between polarity and cell position.

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  • Polarity-driven three-dimensional spontaneous rotation of a cell doublet Nat. Phys. 20, 1194–1203 (2024). https://doi.org/10.1038/s41567-024-02460-w

    résumé

    Mechanical interactions between cells play a fundamental role in the self-organization of organisms. How these interactions drive coordinated cell movement in three dimensions remains unclear. Here we report that cell doublets embedded in a three-dimensional extracellular matrix undergo spontaneous rotations. We investigate the rotation mechanism and find that it is driven by a polarized distribution of myosin within cell cortices. The mismatched orientation of this polarized distribution breaks the doublet mirror symmetry. In addition, cells adhere at their interface through adherens junctions and with the extracellular matrix through focal contacts near myosin clusters. We use a physical theory describing the doublet as two interacting active surfaces to show that rotation is driven by myosin-generated gradients of active tension whose profiles are dictated by interacting cell polarity axes. We also show that three-dimensional shape symmetries are related to broken symmetries of the myosin distribution in cortices. To test for the rotation mechanism, we suppress myosin clusters using laser ablation and generate new myosin clusters by optogenetics. Our work clarifies how polarity-oriented active mechanical forces drive collective cell motion in three dimensions.

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