Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/28522
Title: Combinatorial mathematical modelling approaches to interrogate rear retraction dynamics in 3D cell migration
Authors: Hetmanski, JHR
Jones, MC
Chunara, F
Schwartz, J-M
Caswell, PT
Keywords: coated pits;stiffness;cell polarity;small interfering RNA;soil perturbation;simulation and modeling;actins;biochemical simulations
Issue Date: 10-Mar-2021
Publisher: Public Library of Science (PLoS)
Citation: Hetmanski, J.H.R. et al. (2021) 'Combinatorial mathematical modelling approaches to interrogate rear retraction dynamics in 3D cell migration', PLOS Computational Biology, 17 (3), e1008213, pp. 1 - 35. doi: 10.1371/journal.pcbi.1008213.
Abstract: Cell migration in 3D microenvironments is a complex process which depends on the coordinated activity of leading edge protrusive force and rear retraction in a push-pull mechanism. While the potentiation of protrusions has been widely studied, the precise signalling and mechanical events that lead to retraction of the cell rear are much less well understood, particularly in physiological 3D extra-cellular matrix (ECM). We previously discovered that rear retraction in fast moving cells is a highly dynamic process involving the precise spatiotemporal interplay of mechanosensing by caveolae and signalling through RhoA. To further interrogate the dynamics of rear retraction, we have adopted three distinct mathematical modelling approaches here based on (i) Boolean logic, (ii) deterministic kinetic ordinary differential equations (ODEs) and (iii) stochastic simulations. The aims of this multi-faceted approach are twofold: firstly to derive new biological insight into cell rear dynamics via generation of testable hypotheses and predictions; and secondly to compare and contrast the distinct modelling approaches when used to describe the same, relatively under-studied system. Overall, our modelling approaches complement each other, suggesting that such a multi-faceted approach is more informative than methods based on a single modelling technique to interrogate biological systems. Whilst Boolean logic was not able to fully recapitulate the complexity of rear retraction signalling, an ODE model could make plausible population level predictions. Stochastic simulations added a further level of complexity by accurately mimicking previous experimental findings and acting as a single cell simulator. Our approach highlighted the unanticipated role for CDK1 in rear retraction, a prediction we confirmed experimentally. Moreover, our models led to a novel prediction regarding the potential existence of a ‘set point’ in local stiffness gradients that promotes polarisation and rapid rear retraction.
Description: Data Availability: Model files are available as supplementary material and also available on the BioModels database: https://www.ebi.ac.uk/biomodels/MODEL2103010001.
Supporting information is available online at: https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1008213#sec026 .
URI: https://bura.brunel.ac.uk/handle/2438/28522
DOI: https://doi.org/10.1371/journal.pcbi.1008213
ISSN: 1553-734X
Other Identifiers: ORCiD: Joseph Hetmanski https://orcid.org/0000-0002-1493-351X
ORCiD: Matthew C. Jones https://orcid.org/0000-0003-4723-3277
ORCiD: Jean-Marc Schwartz https://orcid.org/0000-0002-6472-0184
ORCiD: Patrick T. Caswell https://orcid.org/0000-0002-2633-2324
e1008213
Appears in Collections:Dept of Life Sciences Research Papers

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