Substrate disorder promotes cell motility in confluent tissues
In vivo and in vitro cells rely on the support of an underlying biocompatible substrate, such as the extracellular matrix or a culture substrate, to spread and proliferate. The mechanical and chemical properties of such structures play a central role in the dynamical and statistical properties of the tissue. At the cell scale, these substrates are highly disordered. Here, we investigate how spatial heterogeneities of the cell-substrate interaction influence the motility of the cells in a model confluent tissue. We use the Self-Propelled Voronoi model and describe the disorder as a spatially dependent preferred geometry of the individual cells. We found that when the characteristic length scale of the preferred geometry is smaller than the cell size, the tissue is less rigid than its homogeneous counterpart, with a consequent increase in cell motility. This result is in sharp contrast to what has been reported for tissues with heterogeneity in the mechanical properties of the individual cells, where the disorder favors rigidity. Using the fraction of rigid cells, we observe a collapse of the motility data for different model parameters and provide evidence that the rigidity transition in the model tissue is accompanied by the emergence of a spanning cluster of rigid cells.