An elastic sheet that deforms near a solid substrate in a viscous fluid is a situation relevant to various dynamical processes in biology, geophysics and engineering. Here, we study the relaxation dynamics of an elastic plate resting on a thin viscous film that is supported by a solid substrate. By combining scaling analysis, numerical simulations and experiments, we identify asymptotic regimes for the elastohydrodynamic leveling of a surface perturbation of the form of a bump, when the flow is driven by either the elastic bending of the plate or thermal fluctuations. In both cases, two distinct regimes are identified when the bump height is either much larger or much smaller than the thickness of the pre-wetted viscous film. Our analysis reveals a distinct crossover between the similarity exponents with the ratio of the perturbation height to the film height. * acarlson@math.uio.no

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Cellular quiescence is a state of reversible cell cycle arrest that is associated with tissue dormancy. Timely regulated entry into and exit from quiescence is important for processes such as tissue homeostasis, tissue repair, stem cell maintenance, developmental processes, and immunity. However, little is known about processes that control the mechanical adaption to cell behavior changes during the transition from quiescence to proliferation. Here, we show that quiescent human keratinocyte monolayers sustain an actinomyosin-based system that facilitates global cell sheet displacements upon serum-stimulated exit from quiescence. Mechanistically, exposure of quiescent cells to serum-borne mitogens leads to rapid amplification of preexisting contractile sites, leading to a burst in monolayer tension that subsequently drives large-scale displacements of otherwise motility-restricted monolayers. The stress level after quiescence exit correlates with the level of quiescence depth at the time of activation, and a critical stress magnitude must be reached to overcome the cell sheet displacement barrier. The study shows that static quiescent cell monolayers are mechanically poised for motility, and it identifies global stress amplification as a mechanism for overcoming motility restrictions in confined confluent cell monolayers.

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