Literature DB >> 20375040

Cellular automata and integrodifferential equation models for cell renewal in mosaic tissues.

J M Bloomfield1, J A Sherratt, K J Painter, G Landini.   

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.

Mesh:

Year:  2010        PMID: 20375040      PMCID: PMC2988252          DOI: 10.1098/rsif.2010.0071

Source DB:  PubMed          Journal:  J R Soc Interface        ISSN: 1742-5662            Impact factor:   4.118


  23 in total

1.  Modeling of mosaic patterns in chimeric liver and adrenal cortex: algorithmic organogenesis?

Authors:  G Landini; P M Iannaccone
Journal:  FASEB J       Date:  2000-04       Impact factor: 5.191

2.  How far can a juxtacrine signal travel?

Authors:  M R Owen; J A Sherratt; S R Myers
Journal:  Proc Biol Sci       Date:  1999-03-22       Impact factor: 5.349

3.  Mosaic pattern of maternal and paternal keratinocyte clones in normal human epidermis revealed by analysis of X-chromosome inactivation.

Authors:  A Asplund; Z Guo; X Hu; C Wassberg; F Pontén
Journal:  J Invest Dermatol       Date:  2001-07       Impact factor: 8.551

4.  Critical coarsening without surface tension: the universality class of the voter model.

Authors:  I Dornic; H Chaté; J Chave; H Hinrichsen
Journal:  Phys Rev Lett       Date:  2001-07-10       Impact factor: 9.161

Review 5.  Experimental chimeras: current concepts and controversies in normal development and pathogenesis.

Authors:  Y K Ng; P M Iannaccone
Journal:  Curr Top Dev Biol       Date:  1992       Impact factor: 4.897

6.  A continuum approach to modelling cell-cell adhesion.

Authors:  Nicola J Armstrong; Kevin J Painter; Jonathan A Sherratt
Journal:  J Theor Biol       Date:  2006-06-07       Impact factor: 2.691

7.  Simulating invasion with cellular automata: connecting cell-scale and population-scale properties.

Authors:  Matthew J Simpson; Alistair Merrifield; Kerry A Landman; Barry D Hughes
Journal:  Phys Rev E Stat Nonlin Soft Matter Phys       Date:  2007-08-17

8.  Adding adhesion to a chemical signaling model for somite formation.

Authors:  Nicola J Armstrong; Kevin J Painter; Jonathan A Sherratt
Journal:  Bull Math Biol       Date:  2008-09-03       Impact factor: 1.758

9.  The impact of adhesion on cellular invasion processes in cancer and development.

Authors:  Kevin J Painter; Nicola J Armstrong; Jonathan A Sherratt
Journal:  J Theor Biol       Date:  2010-03-25       Impact factor: 2.691

10.  Mathematical modelling and numerical simulation of the morphological development of neurons.

Authors:  Bruce P Graham; Arjen van Ooyen
Journal:  BMC Neurosci       Date:  2006-10-30       Impact factor: 3.288

View more
  3 in total

1.  Models of collective cell behaviour with crowding effects: comparing lattice-based and lattice-free approaches.

Authors:  Michael J Plank; Matthew J Simpson
Journal:  J R Soc Interface       Date:  2012-06-13       Impact factor: 4.118

2.  How much information can be obtained from tracking the position of the leading edge in a scratch assay?

Authors:  Stuart T Johnston; Matthew J Simpson; D L Sean McElwain
Journal:  J R Soc Interface       Date:  2014-08-06       Impact factor: 4.118

3.  BIO-LGCA: A cellular automaton modelling class for analysing collective cell migration.

Authors:  Andreas Deutsch; Josué Manik Nava-Sedeño; Simon Syga; Haralampos Hatzikirou
Journal:  PLoS Comput Biol       Date:  2021-06-15       Impact factor: 4.475

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.