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Comparing individual-based approaches to modelling the self-organization of multicellular tissues

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  • James M Osborne
  • Alexander G Fletcher
  • Joe M Pitt-Francis
  • Philip K Maini
  • David J Gavaghan

Abstract

The coordinated behaviour of populations of cells plays a central role in tissue growth and renewal. Cells react to their microenvironment by modulating processes such as movement, growth and proliferation, and signalling. Alongside experimental studies, computational models offer a useful means by which to investigate these processes. To this end a variety of cell-based modelling approaches have been developed, ranging from lattice-based cellular automata to lattice-free models that treat cells as point-like particles or extended shapes. However, it remains unclear how these approaches compare when applied to the same biological problem, and what differences in behaviour are due to different model assumptions and abstractions. Here, we exploit the availability of an implementation of five popular cell-based modelling approaches within a consistent computational framework, Chaste (http://www.cs.ox.ac.uk/chaste). This framework allows one to easily change constitutive assumptions within these models. In each case we provide full details of all technical aspects of our model implementations. We compare model implementations using four case studies, chosen to reflect the key cellular processes of proliferation, adhesion, and short- and long-range signalling. These case studies demonstrate the applicability of each model and provide a guide for model usage.Author summary: In combination with molecular and live-imaging techniques, computational modelling plays an increasingly important role in the study of tissue growth and renewal. To this end a variety of cell-based modelling approaches have been developed, ranging in complexity from lattice-based cellular automata to lattice-free models that treat cells as point-like particles or extended shapes. However, it remains unclear how these approaches compare when applied to the same biological problem, and under which circumstances each approach is valid. Here we implement five classes of such model in a consistent computational framework, Chaste. We apply each model to four simulation studies, chosen to illustrate how the cellular processes such as proliferation, adhesion, and short- and long-range signalling may be implemented in each model. These case studies demonstrate the applicability of each model and highlight where one may expect to see qualitative differences between model behaviours. Taken together, these findings provide a guide for model usage.

Suggested Citation

  • James M Osborne & Alexander G Fletcher & Joe M Pitt-Francis & Philip K Maini & David J Gavaghan, 2017. "Comparing individual-based approaches to modelling the self-organization of multicellular tissues," PLOS Computational Biology, Public Library of Science, vol. 13(2), pages 1-34, February.
  • Handle: RePEc:plo:pcbi00:1005387
    DOI: 10.1371/journal.pcbi.1005387
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    References listed on IDEAS

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    1. Gary R Mirams & Christopher J Arthurs & Miguel O Bernabeu & Rafel Bordas & Jonathan Cooper & Alberto Corrias & Yohan Davit & Sara-Jane Dunn & Alexander G Fletcher & Daniel G Harvey & Megan E Marsh & J, 2013. "Chaste: An Open Source C++ Library for Computational Physiology and Biology," PLOS Computational Biology, Public Library of Science, vol. 9(3), pages 1-8, March.
    2. Peter Buske & Jörg Galle & Nick Barker & Gabriela Aust & Hans Clevers & Markus Loeffler, 2011. "A Comprehensive Model of the Spatio-Temporal Stem Cell and Tissue Organisation in the Intestinal Crypt," PLOS Computational Biology, Public Library of Science, vol. 7(1), pages 1-13, January.
    3. Sabine Schilling & Maria Willecke & Tinri Aegerter-Wilmsen & Olaf A Cirpka & Konrad Basler & Christian von Mering, 2011. "Cell-Sorting at the A/P Boundary in the Drosophila Wing Primordium: A Computational Model to Consolidate Observed Non-Local Effects of Hh Signaling," PLOS Computational Biology, Public Library of Science, vol. 7(4), pages 1-12, April.
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