ArticleJournal of the Royal Society, Interface2010
Cellular automata and integrodifferential equation models for cell renewal in mosaic tissues.
Article in Journal of the Royal Society, Interface, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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4 citing papers in PubMed.
- Learning spatio-temporal patterns with Neural Cellular Automata.PLoS computational biology · 2024Article
- BIO-LGCA: A cellular automaton modelling class for analysing collective cell migration.PLoS computational biology · 2021Article
- How much information can be obtained from tracking the position of the leading edge in a scratch assay?Journal of the Royal Society, Interface · 2014Article
- Models of collective cell behaviour with crowding effects: comparing lattice-based and lattice-free approaches.Journal of the Royal Society, Interface · 2012Article
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4 authors.
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Abstract
Mosaic tissues are composed of two or more genetically distinct cell types. They occur naturally, and are also a useful experimental method for exploring tissue growth and maintenance. By marking the different cell types, one can study the patterns formed by proliferation, renewal and migration. Here, we present mathematical modelling suggesting that small changes in the type of interaction that cells have with their local cellular environment can lead to very different outcomes for the composition of mosaics. In cell renewal, proliferation of each cell type may depend linearly or nonlinearly on the local proportion of cells of that type, and these two possibilities produce very different patterns. We study two variations of a cellular automaton model based on simple rules for renewal. We then propose an integrodifferential equation model, and again consider two different forms of cellular interaction. The results of the continuous and cellular automata models are qualitatively the same, and we observe that changes in local environment interaction affect the dynamics for both. Furthermore, we demonstrate that the models reproduce some of the patterns seen in actual mosaic tissues. In particular, our results suggest that the differing patterns seen in organ parenchymas may be driven purely by the process of cell replacement under different interaction scenarios.
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