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Daraf, L.

Publications and source records attributed to Daraf, L..

2 recordsLinked to original sources

Local mechanical gradients underlie coordinated cascades of epithelial cell-cycle advance

Cell division mechanically perturbs the local environment in epithelial tissues, yet whether and how these perturbations propagate to coordinate cell-cycle progression across neighboring cells remains unclear. Here, we combine live cell-cycle tracking with mechanical analysis to examine how division events organize in space and time. We find that coordinated changes and spatial gradients in forces, morphology, and dynamics precede synchronized G1[->]S transitions in nearby cells. These transitions emerge within localized high-tension zones and give rise to spatiotemporal clusters of cell divisions, indicating that division events are mechanically coupled and propagate across neighboring cells. Supporting this biophysical picture, similar mechanical patterns arising from cell extrusion are sufficient to induce cell-cycle re-entry in neighboring cells. Together, these findings suggest a mechanically mediated framework for coordinated proliferation, possibly driven by positive mechanical feedback.

biophysics↗

3D-printed toolkit for regulating epithelial unjamming

During wound healing and cancer invasion, epithelial monolayers transition from a solid-like, jammed state to a fluid-like unjammed state. However, affordable and accessible tools for modeling and precise tuning of this response remain limited. Here, we present a simple, lithography-free 3D-printed toolkit of customizable inserts and scratchers for fabricating micro-gaps with defined geometries and widths down to [~]50 {micro}m, without requiring cleanroom facilities or specialized expertise. Using epithelial monolayers, we demonstrate that gap width fundamentally regulates unjamming dynamics. Narrow gaps induced rapid, coordinated migration with high initial velocities, whereas wide gaps suppressed early unjamming and produced slower, spatially heterogeneous closure. Cell shape dynamics confirmed conserved elongation, cell rounding, and closure behaviors across conditions. The presented toolkit provides new opportunities for investigating the mechanical and molecular mechanisms that regulate epithelial plasticity, enabling fine control of unjamming transitions and allowing the modeling of both healthy and pathological wound-response regimes.

biophysics↗