Stochastic multiscale models of cell populations: asymptotic and numerical mehods Articles uri icon

publication date

  • February 2015

start page

  • 64

end page

  • 93


  • 1


  • 10

International Standard Serial Number (ISSN)

  • 0973-5348


  • In this paper we present a new methodology that allows us to formulate and analyse stochastic multiscale models of the dynamics of cell populations. In the spirit of existing hybrid multiscale models, we set up our model in a hierarchical way according to the characteristic
    time scales involved, where the stochastic population dynamics is governed by the birth and death rates as prescribed by the corresponding intracellular pathways (e.g. stochastic cell-cycle model). The feed-back loop is closed by the coupling between the dynamics of the population
    and the intracellular dynamics via the concentration of oxygen: Cells consume oxygen which, in turn, regulate the rate at which cells proceed through their cell-cycle. The coupling between intracellular and population dynamics is carried out through a novel method to obtain the birth
    rate from the stochastic cell-cycle model, based on a mean-first passage time approach. Cell proliferation is assumed to be activated when one or more of the proteins involved in the cell-cycle regulatory pathway hit a threshold. This view allows us to calculate the birth rate as a
    function of the age of the cell and the extracellular oxygen in terms of the corresponding mean-first passage time. We then proceed to formulate the stochastic dynamics of the population of cells in terms of an age-structured Master Equation. Further, we have developed generalisations of asymptotic (WKB) methods for our age-structured Master Equation as well as a τ-leap method to simulate the evolution of our age-structured population. Finally, we illustrate this general methodology with a particular example of a cell population where progression through the cell-cycle is regulated by the availability of oxygen


  • Mathematics


  • multiscale modelling; stochastic modelling; cancer; cell-cycle