Friction patterns guide actin network contraction.

The shape of cells is the outcome of the balance of inner forces produced by the actomyosin network and the resistive forces produced by cell adhesion to their environment. The specific contributions of contractile, anchoring and friction forces to network deformation rate and orientation are difficult to disentangle in living cells where they influence each other. Here, we reconstituted contractile actomyosin networks in vitro to study specifically the role of the friction forces between the network and its anchoring substrate. To modulate the magnitude and spatial distribution of friction forces, we used glass or lipids surface micropatterning to control the initial shape of the network. We adapted the concentration of Nucleating Promoting Factor on each surface to induce the assembly of actin networks of similar densities and compare the deformation of the network toward the centroid of the pattern shape upon myosin-induced contraction. We found that actin network deformation was faster and more coordinated on lipid bilayers than on glass, showing the resistance of friction to network contraction. To further study the role of the spatial distribution of these friction forces, we designed heterogeneous micropatterns made of glass and lipids. The deformation upon contraction was no longer symmetric but biased toward the region of higher friction. Furthermore, we showed that the pattern of friction could robustly drive network contraction and dominate the contribution of asymmetric distributions of myosins. Therefore, we demonstrate that during contraction, both the active and resistive forces are essential to direct the actin network deformation.

Crawling, waving, inch worming, dilating, and pivoting mechanics of migrating cells: Lessons from Ken Jacobson.

Research on the locomotion of single cells on hard, flat surfaces brought insight into the mechanisms of leading-edge protrusion, spatially graded adhesion, front-rear coordination, and how intracellular and traction forces are harnessed to execute various maneuvers. Here, we highlight how, by studying a variety of cell types, shapes, and movements, Ken Jacobson and his collaborators made several discoveries that triggered the mechanistic understanding of cell motility. We then review the recent advancements and current perspectives in this field.

Synchronization and locking in oscillators with flexible periods.

Entrainment of a nonlinear oscillator by a periodic external force is a much studied problem in nonlinear dynamics and characterized by the well-known Arnold tongues. The circle map is the simplest such system allowing for stable N:M entrainment where the oscillator produces N cycles for every M stimulus cycles. There are a number of experiments that suggest that entrainment to external stimuli can involve both a shift in the phase and an adjustment of the intrinsic period of the oscillator. Motivated by a recent model of Loehr et al. [J. Exp. Psychol.: Hum. Percept. Perform. 37, 1292 (2011)], we explore a two-dimensional map in which the phase and the period are allowed to update as a function of the phase of the stimulus. We characterize the number and stability of fixed points for different N:M-locking regions, specifically, 1:1, 1:2, 2:3, and their reciprocals, as a function of the sensitivities of the phase and period to the stimulus as well as the degree that the oscillator has a preferred period. We find that even in the limited number of locking regimes explored, there is a great deal of multi-stability of locking modes, and the basins of attraction can be complex and riddled. We also show that when the forcing period changes between a starting and final period, the rate of this change determines, in a complex way, the final locking pattern.