Abstract

In the last decade, the cellular Potts model has been extensively used to model interacting cell systems at the tissue-level. However, in {\bf early} applications of this model, cell movement was taken as a consequence of membrane fluctuations due to cell-cell interactions, or as a response to an external chemotactic gradient. Recent findings have shown that eukaryotic cells can exhibit persistent displacements across scales larger than cell size, even in the absence of external signals. Persistent cell motion has been incorporated to the cellular Potts model by many authors in the context of collective motion, chemotaxis and morphogenesis. In this paper, we use the cellular Potts model in combination with a random field applied over each cell. This field promotes a uniform cell motion in a given direction during a certain time interval, after which the movement direction changes. The dynamics of the direction is coupled to a first order autoregressive process. We investigated statistical properties, such as the mean-squared displacement and spatio-temporal correlations, associated to these self-propelled {\it in silico} cells in different conditions. The proposed model emulates many properties observed in different experimental setups. By studying low and high density cultures, we find that cell-cell interactions decrease the effective persistent time.

Highlights

  • Biological development is a clear example of a complex system and is the result of several morphogenetic processes such as: cell adhesion, cell division, migration, among others [1]

  • Since the classical Steinberg experiments, it has been demonstrated that differential adhesion is a key ingredient for cell rearrangement and cell sorting [53, 54]

  • Graner and Glazier have shown that the cellular Potts models (CPM) model with solely differential adhesion, as driving force, is able to generate cell sorting [16]

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Summary

Introduction

Biological development is a clear example of a complex system and is the result of several morphogenetic processes such as: cell adhesion, cell division, migration, among others [1]. Important insights about the principles involved in the biological development can be extracted from mathematical models used in many works over the last decade [2]. There is still no standard model to describe interacting cells in all scales. Continuous models to study combinations of chemical reaction kinetics and cell mobilities through diffusional processes have been useful at tissue-level scales [5, 6]. Simplified continuous models of self-propelled particles have been useful to uncover a new kind of phase transition in collective motions [7,8,9,10,11,12], (see [13] for a review of motility-induced phase separation)

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