Jef Vangheel, Herman Ramon, Bart Smeets
In morphogenesis and disease, biological tissues may exhibit diverse mechanical properties due to their capacity to switch between fluidlike and solidlike states. Here, we introduce a foam model to investigate how active mechanical properties and cellular interactions govern this fluid-to-solid transition in active cell monolayers. This model explicitly represents three-dimensional cell shapes and describes cell-cell interactions via discrete interacting surfaces. Simulations reveal that cell-cell adhesive tension promotes tissue fluidization in high-adhesive tissues, where it mainly promotes cell deformability, while it induces solidification in the low-adhesive regime, where it prevents cell-cell debonding. Moreover, we study the dynamic role of adhesive ligand turnover through an effective intercellular friction. Through simulated shear experiments, we find that intercellular friction strongly suppresses neighbor exchanges, but does not lead to solidlike tissue properties. We discuss the implications of our results for understanding the relationship between fluidization and the partial epithelial-mesenchymal transition, highlighting how differences in adhesion dynamics and intercellular friction may reconcile conflicting observations in tissue mechanics and cancer metastasis.