ﻻ يوجد ملخص باللغة العربية
Cell crawling is critical to biological development, homeostasis and disease. In many cases, cell trajectories are quasi-random-walk. In vitro assays on flat surfaces often described such quasi-random-walk cell trajectories as approximations to a solution of a Langevin process. However, experiments show quasi-diffusive behavior at small timescales, indicating that instantaneous velocity and velocity autocorrelations are not well-defined. We propose to characterize mean-squared cell displacement using a modified Furth equation with three temporal and spatial regimes: short- and long-time/range diffusion and intermediate time/range ballistic motion. This analysis collapses mean-squared displacements of previously published experimental data onto a single-parameter family of curves, allowing direct comparison between movement in different cell types, and between experiments and numerical simulations. Our method also show that robust cell-motility quantification requires an experiment with a maximum interval between images of a few percent of the cell-motion persistence time or less, and a duration of a few orders-of-magnitude longer than the cell-motion persistence time or more.
Collections of cells exhibit coherent migration during morphogenesis, cancer metastasis, and wound healing. In many cases, bigger clusters split, smaller sub-clusters collide and reassemble, and gaps continually emerge. The connections between cell-l
Amoeboid cell migration is characterized by frequent changes of the direction of motion and resembles a persistent random walk on long time scales. Although it is well known that cell migration is typically driven by the actin cytoskeleton, the cause
Key to collective cell migration is the ability of cells to rearrange their position with respect to their neighbors. Recent theory and experiments demonstrated that cellular rearrangements are facilitated by cell shape, with cells having more elonga
Cell migration, which can be significantly affected by intracellular signaling pathways (ICSP) and extracellular matrix (ECM), plays a crucial role in many physiological and pathological processes. The efficiency of cell migration, which is typically
Cell migration plays essential roles in development, wound healing, diseases, and in the maintenance of a complex body. Experiments in collective cell migration generally measure quantities such as cell displacement and velocity. The observed short-t