Theory and simulation for equilibrium glassy dynamics in cellular Potts model of confluent biological tissue

Glassy dynamics in a confluent monolayer is indispensable in morphogenesis, wound healing, bronchial asthma, and many others; a detailed theoretical framework for such a system is, therefore, important. Vertex-model (VM) simulations have provided crucial insights into the dynamics of such systems, but their nonequilibrium nature makes theoretical development difficult. The cellular Potts model (CPM) of confluent monolayers provides an alternative model for such systems with a well-defined equilibrium limit. We combine numerical simulations of the CPM and an analytical study based on one of the most successful theories of equilibrium glass, the random first-order transition theory, and develop a comprehensive theoretical framework for a confluent glassy system. We find that the glassy dynamics within the CPM is qualitatively similar to that in the VM. Our study elucidates the crucial role of geometric constraints in bringing about two distinct regimes in the dynamics, as the target perimeter P_{0} is varied. The unusual sub-Arrhenius relaxation results from the distinctive interaction potential arising from the perimeter constraint in such systems. The fragility of the system decreases with increasing P_{0} in the low-P_{0} regime, whereas the dynamics is independent of P_{0} in the other regime. The rigidity transition, found in the VM, is absent within the CPM; this difference seems to come from the nonequilibrium nature of the former. We show that the CPM captures the basic phenomenology of glassy dynamics in a confluent biological system via comparison of our numerical results with existing experiments on different systems.