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Stochastic Multiscale Models of Cell Population Dynamics: Asymptotic and Numerical Methods

机译:细胞种群动态随机多尺度模型:渐近和数值方法

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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). "file 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 dynainics 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 tau-leap method to simulate the evolution of our age-structured population. Finally, we illustrate Otis general methodology with a particular example of a cell population where progression through the cell-cycle is regulated by the availability of oxygen.
机译:在本文中,我们提出了一种新的方法,使我们能够制定和分析细胞种群动态的随机多尺度模型。本着现有混合多尺度模型的精神,我们根据涉及的特征时间尺度以分层方式建立模型,其中随机种群动态由相应细胞内途径(例如随机细胞)规定的出生率和死亡率决定-周期模型)。 “文件反馈回路是通过种群动态与细胞内动力学之间通过氧气浓度的耦合而封闭的:细胞消耗氧气,氧气又调节着细胞通过其细胞周期的速率。这种耦合基于平均-第一次通过时间的方法,通过一种新颖的方法从随机细胞周期模型中获得细胞动力学与种群动力学之间的联系,并假定当涉及一种或多种蛋白质时,细胞增殖被激活在细胞周期调节途径中的出生率达到阈值,该观点使我们能够根据相应的均值优先通过时间来计算出生率与细胞年龄和细胞外氧的关系。基于年龄结构的Master方程的细胞种群随机动力学进一步,我们为年龄结构的Master E开发了渐近(WKB)方法的推广公式和tau-leap方法来模拟我们年龄结构人口的演变。最后,我们用一个特定的细胞种群示例说明了Otis的一般方法,其中整个细胞周期的进程受氧气的可用性调节。

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