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Intercellular friction and motility drive orientational order in cell monolayers
Michael Chiang1, Austin Hopkins2, Benjamin Loewe1,3
1Scottish Universities Physics Alliance, School of Physics and Astronomy, University of Edinburgh, Edinburgh EH9 3FD, United Kingdom.
Intercellular friction in cell monolayers drives a solid-liquid transition, leading to nematic order and topological defects. These defects, coupled with cell overlap, may mediate cell extrusion during tissue development and disease.
Area of Science:
- Physics of complex systems
- Biophysics
- Computational biology
Background:
- Spatiotemporal patterns in multicellular systems are crucial for understanding tissue dynamics in development and disease.
- Cellular collectives exhibit emergent behaviors influenced by cell properties and interactions.
Purpose of the Study:
- To numerically investigate the behavior of deformable cell monolayers with intercellular friction.
- To explore the relationship between intercellular friction, cell motility, and emergent order.
- To model the coupling between topological defects and cellular mechanics.
Main Methods:
- Multiphase field modeling of near-confluent cell monolayers.
- Numerical simulations varying intercellular friction and cell motility.
- Analysis of solid-liquid transitions, nematic order, and topological defects.
Main Results:
- Varying friction and motility induce a solid-liquid transition and local nematic order.
- Intercellular friction increases monolayer viscosity, enhancing flow correlations and nematic order.
- Hexatic and nematic order are coupled; a model explains defect colocalization with cell overlap.
Conclusions:
- Results provide a mechanical basis for observed nematic/hexatic order in multicellular systems.
- Topological defects coinciding with cell overlap suggest a mechanism for cellular extrusion.
- The study identifies a generic pathway to couple topological and physical effects in cellular collectives.
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