The Mathematical Institute, University of Oxford, Eprints Archive

An integrative computational model for intestinal tissue renewal

Leeuwen, I M M and Mirams, G R and Walter, A and Fletcher, A and Murray, P J and Osborne, J and Varma, S and Young, S J and Cooper, J and Doyle, B and Pitt-Francis, J and Momtahan, L and Pathmanathan, P. and Whiteley, J. P. and Chapman, S. J. and Gavaghan, D. J. and Jensen, O E and King, J. R. and Maini, P. K. and Waters, S. L. and Byrne, H. M. (2009) An integrative computational model for intestinal tissue renewal. Cell Proliferation .

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Abstract

Objectives

The luminal surface of the gut is lined with a monolayer of epithelial cells that acts as a nutrient absorptive engine and protective barrier. To maintain its integrity and functionality, the epithelium is renewed every few days. Theoretical models are powerful tools that can be used to test hypotheses concerning the regulation of this renewal process, to investigate how its dysfunction can lead to loss of homeostasis and neoplasia, and to identify potential therapeutic interventions. Here we propose a new multiscale model for crypt dynamics that links phenomena occurring at the subcellular, cellular and tissue levels of organisation.

Methods

At the subcellular level, deterministic models characterise molecular networks, such as cell-cycle control and Wnt signalling. The output of these models determines the behaviour of each epithelial cell in response to intra-, inter- and extracellular cues. The modular nature of the model enables us to easily modify individual assumptions and analyse their effects on the system as a whole.

Results

We perform virtual microdissection and labelling-index experiments, evaluate the impact of various model extensions, obtain new insight into clonal expansion in the crypt, and compare our predictions with recent mitochondrial DNA mutation data.

Conclusions

We demonstrate that relaxing the assumption that stem-cell positions are fixed enables clonal expansion and niche succession to occur. We also predict that the presence of extracellular factors near the base of the crypt alone suffices to explain the observed spatial variation in nuclear beta-catenin levels along the crypt axis.

Item Type:Article
Subjects:A - C > Biology and other natural sciences
Research Groups:Oxford Centre for Industrial and Applied Mathematics
ID Code:910
Deposited By:Ruth Preston
Deposited On:25 Mar 2010 14:49
Last Modified:27 Dec 2012 20:59

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