Julia Yeomans OBE FRS

Abstract:

Many cells in the human body have to move through dense complex fluids such as various cells in the extracellular matrix or bacteria in mucus. While the motion of swimming bacteria in simple Newtonian fluids can be well quantified using continuum low Reynolds number hydrodynamics, the presence of supramolecular elements such as biopolymers leads to a much more complex behavior. Although the presence of polymers generally lowers particle mobility, surprisingly, several experiments have shown that bacterial speeds increase in polymeric fluids [1, 2, 3, 4], but there is no clear understanding why. We perform extensive coarse-grained MPCD simulations of a bacterium swimming in explicitly modeled solutions of supramolecular model polymers of different lengths, stiffness and densities. We observe an increase of up to 60% in swimming speed with polymer density and show that this is a consequence of a depletion of polymers in the vicinity of the bacterium leading to an effective slip. However, depletion alone cannot explain the large speed-up, but coupling to the chirality of the bacterial flagellum is essential.

Abstract:

Morphological changes during development, tissue repair, and disease largely rely on coordinated cell movements and are controlled by the tissue environment. Epithelial cell sheets are often subjected to large scale deformation during tissue formation. The active mechanical environment in which epithelial cells operate have the ability to promote collective oscillations, but how these cellular movements are generated and relate to collective migration remains unclear. Here, combining in vitro experiments and computational modelling we describe a novel mode of collective oscillations in confined epithelial tissues where the oscillatory motion is the dominant contribution to the cellular movements. We show that epithelial cells exhibit large-scale coherent oscillations when constrained within micro-patterns of varying shapes and sizes, and that their period and amplitude are set by the smallest confinement dimension. Using molecular perturbations, we then demonstrate that force transmission at cell-cell junctions and its coupling to cell polarity are pivotal for the generation of these collective movements. We find that the resulting tissue deformations are sufficient to trigger mechanotransduction within cells, potentially affecting a wide range of cellular processes.

Abstract:

Microbial flagellates typically inhabit complex suspensions of polymeric material which can impact the swimming speed of motile microbes, filter-feeding of sessile cells, and the generation of biofilms. There is currently a need to better understand how the fundamental dynamics of polymers near active cells or flagella impacts these various phenomena, in particular the hydrodynamic and steric influence of a rotating helical filament on suspended polymers. Our Stokesian dynamics simulations show that as a stationary rotating helix pumps fluid along its long axis, polymers migrate radially inwards while being elongated. We observe that the actuation of the helix tends to increase the probability of finding polymeric material within its pervaded volume. This accumulation of polymers within the vicinity of the helix is stronger for longer polymers. We further analyse the stochastic work performed by the helix on the polymers and show that this quantity is positive on average and increases with polymer contour length.