# Mechanochemical subcellular-element model of crawling cells

## TL;DR

This paper introduces a mechanochemical model of cell crawling that links intracellular chemical signals to movement direction and distance, providing insights into force-free migration mechanisms.

## Contribution

It presents the first fully force-free cell migration model driven by intracellular chemical reactions, integrating reaction-diffusion dynamics with mechanical processes.

## Key findings

- Chemical dependence of adhesion controls crawling direction.
- Traveling chemical waves influence cell movement.
- Traction force analysis aligns with experimental data.

## Abstract

Constructing physical models of living cells and tissues is an extremely challenging task because of the high complexities of both intra- and intercellular processes. In addition, the force that a single cell generates vanishes in total due to the law of action and reaction. The typical mechanics of cell crawling involve periodic changes in the cell shape and in the adhesion characteristics of the cell to the substrate. However, the basic physical mechanisms by which a single cell coordinates these processes cooperatively to achieve autonomous migration are not yet well understood. To obtain a clearer grasp of how the intracellular force is converted to directional motion, we develop a basic mechanochemical model of a crawling cell based on subcellular elements with the focus on the dependence of the protrusion and contraction as well as the adhesion and deadhesion processes on intracellular biochemical signals. By introducing reaction-diffusion equations that reproduce traveling waves of local chemical concentrations, we clarify that the chemical dependence of the cell-substrate adhesion dynamics determines the crawling direction and distance with one chemical wave. Finally, we also perform multipole analysis of the traction force to compare it with the experimental results. To our knowledge, our present work is the first study that accomplishes fully force-free migration utilizing intracellular chemical reactions. Although the detailed mechanisms of actual cells are far more complicated than our simple model, we believe that this mechanochemical model is a good prototype for more realistic models.