Abstract

Model simulations indicate that the response of growing cell populations on mechanical stress follows the same functional relationship and is predictable over different cell lines and growth conditions despite experimental response curves look largely different. We develop a hybrid model strategy in which cells are represented by coarse-grained individual units calibrated with a high resolution cell model and parameterized by measurable biophysical and cell-biological parameters. Cell cycle progression in our model is controlled by volumetric strain, the latter being derived from a bio-mechanical relation between applied pressure and cell compressibility. After parameter calibration from experiments with mouse colon carcinoma cells growing against the resistance of an elastic alginate capsule, the model adequately predicts the growth curve in i) soft and rigid capsules, ii) in different experimental conditions where the mechanical stress is generated by osmosis via a high molecular weight dextran solution, and iii) for other cell types with different growth kinetics from the growth kinetics in absence of external stress. Our model simulation results suggest a generic, even quantitatively same, growth response of cell populations upon externally applied mechanical stress, as it can be quantitatively predicted using the same growth progression function.

Highlights

  • Mechanotransduction is the mechanism by which cells transform an external mechanical stimulus into internal signals

  • We studied data from two different experimental setups that monitor the growth of tumor cells under mechanical compression

  • We have developed an agent-based model with measurable biophysical and cell-biological parameters that can simulate both experiments

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Summary

Introduction

Mechanotransduction is the mechanism by which cells transform an external mechanical stimulus into internal signals. Helmlinger et al (1997) and later Cheng et al (2009) and Mills et al (2014) [8,9,10] experimentally investigated the growth of spheroids embedded in agarose gel pads at varying agarose concentration as a tunable parameter for the stiffness of the surrounding medium. Other approaches such as the application of an osmotic pressure determined by a dextran polymer solution have been developed to investigate the impact of external pressure on spheroid growth [11]. The model developed in that reference has no precise notion of cell shape, does not permit definition of cell volume, pressure and compression cannot be physically correctly related [21]

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