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Juan C. Lasheras

Publications and source records attributed to Juan C. Lasheras.

3 recordsLinked to original sources

Interaction of a migrating cell monolayer with a flexible fiber

Mechanical forces influence the development and behavior of biological tissues. In many situations these forces are exerted or resisted by elastic compliant structures such as the own-tissue cellular matrix or other surrounding tissues. This kind of tissue-elastic body interactions are also at the core of many state-of-the-art {\it in situ} force measurement techniques employed in biophysics. This creates the need to model tissue interaction with the surrounding elastic bodies that exert these forces, raising the question: which are the minimum ingredients needed to describe such interactions? We conduct experiments where migrating cell monolayers push on carbon fibers as a model problem. Although the migrating tissue is able to bend the fiber for some time, it eventually recoils before coming to a stop. This stop occurs when cells have performed a fixed mechanical work on the fiber, regardless of its stiffness. Based on these observations we develop a minimal active-fluid model that reproduces the experiments and predicts quantitatively relevant features of the system. This minimal model points out the essential ingredients needed to describe tissue-elastic solid interactions: an effective inertia and viscous stresses.

physics.bio-ph

Self-organized mechano-chemical dynamics in amoeboid locomotion of Physarum fragments

The aim of this work is to quantify the spatio-temporal dynamics of flow-driven amoeboid locomotion in small ($\sim$100 $μ$m) fragments of the true slime mold \phys {\it polycephalum}. In this model organism, cellular contraction drives intracellular flows, and these flows transport the chemical signals that regulate contraction in the first place. As a consequence of these non-linear interactions, a diversity of migratory behaviors can be observed in migrating \phys fragments. To study these dynamics, we measure the spatio-temporal distributions of the velocities of the endoplasm and ectoplasm of each migrating fragment, the traction stresses it generates on the substratum, and the concentration of free intracellular calcium. Using these unprecedented experimental data, we classify migrating \phys fragments according to their dynamics, finding that they often exhibit spontaneously coordinated waves of flow, contractility and chemical signaling. We show that \phys fragments exhibiting symmetric spatio-temporal patterns of endoplasmic flow migrate significantly slower than fragments with asymmetric patterns. In addition, our joint measurements of ectoplasm velocity and traction stress at the substratum suggest that forward motion of the ectoplasm is enabled by a succession of stick-slip transitions, which we conjecture are also organized in the form of waves. Combining our experiments with a simplified convection-diffusion model, we show that the convective transport of calcium ions may be key for establishing and maintaining the spatio-temporal patterns of calcium concentration that regulate the generation of contractile forces.

q-bio.CB

Distribution of Traction Forces and Intracellular Markers Associated with Shape Changes During Amoeboid Cell Migration

During migration, amoeboid cells perform a cycle of quasi-periodic repetitive events (motility cycle). the cell length and the strain energy exchanged with the substrate oscillate in time with an average frequency, f, on top of which are imposed smaller random fluctuations. the fact that a considerable portion of the changes in cell shape are due to periodic repetitive events enables the use of conditional statistics methods to analyze the network of biochemical processes involved in cell motility. taking advan- tage of this cyclic nature, we apply Principal Component analysis (PCa) and phase- average statistics to analyze the dominant modes of shape change and their association to the activity and localization of molecular motors. We analyze time-lapse measure- ments of cell shape, traction forces and fluorescence from green fluorescent protein (GfP) reporters for f-actin in Dictyostelium cells undergoing guided chemotactic migration. using wild-type cells (wt) as reference, we investigated the contractile and actin crosslinking functions of myosin II by studying myosin II heavy chain null mutant cells (mhcA-) and myosin II essential light chain null cells (mlcE-).

q-bio.CB