Relaxation Dynamics in Persistent Epithelial Tissues

Abstract

Cell monolayers and epithelial tissues display slow dynamics during the liquid-glass transitions, a phenomenon with direct relevance to embryogenesis, tumor metastases, and wound healing. In active cells, persistent motion and cell deformation compete, significantly influencing relaxation dynamics. Here, we numerically construct the liquid-glass transition phase diagram for two-dimensional polydisperse persistent cells. We employ cage-relative measures and conduct extensive simulations to eliminate the influence of system size effects. These effects arise from long-wavelength fluctuations in nearly equilibrated cells and a combination of long-wavelength fluctuations and non-equilibrium effects in highly persistent cells. Our study unveils distinctive intermittent dynamics associated with intermittent T1 transitions in highly persistent cells, where the velocity correlates over space with a characteristic length $\xi$. The $\alpha$ relaxation time exhibits a universal power-law dependence on the irreversible T1 transition rate, $\Gamma_{\rm{T1}}^{\rm irr}$, multiplied by ${\rm exp}(\xi)$. Here, $\xi$ vanishes in nearly equilibrated cells, and $\Gamma_{\rm{T1}}^{\rm irr}$ diminishes towards the mode-coupling glass transition point.