Abstract
The collective dynamics of multicellular systems arise from the interplay of a few fundamental elements: growth, division and apoptosis of single cells; their mechanical and adhesive interactions with neighboring cells and the extracellular matrix; and the tendency of polarized cells to move. Micropatterned substrates are increasingly used to dissect the relative roles of these fundamental processes and to control the resulting dynamics. Here we show that a unifying computational framework based on the cellular Potts model can describe the experimentally observed cell dynamics over all relevant length scales. For single cells, the model correctly predicts the statistical distribution of the orientation of the cell division axis as well as the final organisation of the two daughters on a large range of micropatterns, including those situations in which a stable configuration is not achieved and rotation ensues. Large ensembles migrating in heterogeneous environments form non-adhesive regions of inward-curved arcs like in epithelial bridge formation. Collective migration leads to swirl formation with variations in cell area as observed experimentally. In each case, we also use our model to predict cell dynamics on patterns that have not been studied before.
Highlights
Adhesive micropatterns (MP) determine the spatial distribution of the extracellular matrix (ECM) and allow us to investigate and control cell shape, structure and function through experimental design
The collective dynamics of many cells is more than the sum of its parts
We focus on cellular dynamics on adhesive micropatterns as an especially successful approach to investigate and control complex cell behaviour
Summary
Adhesive micropatterns (MP) determine the spatial distribution of the extracellular matrix (ECM) and allow us to investigate and control cell shape, structure and function through experimental design. They have emerged as an extremely versatile tool to investigate the inner workings of cells [1]. They are especially suited to achieve a quantitative understanding of how cells respond to external cues. Pioneering work with adhesive micropatterns has demonstrated the importance of the ECM-geometry for the survival of cells [2]. Originally designed to immobilize single cells, micropatterns have been extensively used to study their dynamic processes, including the different phases of cell spreading [3] or migration on stripe patterns with a focus on cell speed and persistency [11, 12]
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