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首页> 外文期刊>Journal of Theoretical Biology >Stochastic multi-scale, models of competition within heterogeneous cellular populations: Simulation methods and mean-field analysis
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Stochastic multi-scale, models of competition within heterogeneous cellular populations: Simulation methods and mean-field analysis

机译:随机多尺度,异构蜂窝种群中的竞争模型:仿真方法和平均场分析

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We propose a modelling framework to analyse the stochastic behaviour of heterogeneous, multi-scale cellular populations. We illustrate our methodology with a particular example in which we study a population with an oxygen-regulated proliferation rate. Our formulation is based on an age-dependent stochastic process. Cells within the population are characterised by their age (i.e. time elapsed since they were born). The age-dependent (oxygen-regulated) birth rate is given by a stochastic model of oxygen-dependent cell cycle progression. Once the birth rate is determined, we formulate an age-dependent birth-and-death process, which dictates the time evolution of the cell population. The population is under a feedback loop which controls its steady state size (carrying capacity): cells consume oxygen which in turn fuels cell proliferation. We show that our stochastic model of cell cycle progression allows for heterogeneity within the cell population induced by stochastic effects. Such heterogeneous behaviour is reflected in variations in the proliferation rate. Within this set-up, we have established three main results. First, we have shown that the age to the G1/S transition, which essentially determines the birth rate, exhibits a remarkably simple scaling behaviour. Besides the fact that this simple behaviour emerges from a rather complex model, this allows for a huge simplification of our numerical methodology. A further result is the observation that heterogeneous populations undergo an internal process of quasi-neutral competition. Finally, we investigated the effects of cell-cycle-phase dependent therapies (such as radiation therapy) on heterogeneous populations. In particular, we have studied the case in which the population contains a quiescent sub-population. Our mean-field analysis and numerical simulations confirm that, if the survival fraction of the therapy is too high, rescue of the quiescent population occurs. This gives rise to emergence of resistance to therapy since the rescued population is less sensitive to therapy. (C) 2016 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license.
机译:我们提出了一种建模框架来分析异质,多尺度蜂窝种群的随机行为。我们用氧气调节增殖率研究人群的特定实例说明了我们的方法。我们的配方基于年龄依赖的随机过程。人群中的细胞的特征在于他们的年龄(即自出生以来经过的时间)。依赖于年龄依赖性(氧气调节的)出生率由氧依赖性细胞周期进展的随机模型给出。一旦确定出生率,我们制定了依赖年龄依赖性的出生和死亡过程,这决定了细胞群的时间演变。人口在反馈回路下,控制其稳态尺寸(承载能力):细胞消耗氧气,其燃料细胞增殖。我们表明,我们的细胞周期进程的随机模型允许随机效应引起的细胞群内的异质性。这种异质行为被反映在增殖率的变化中。在此设置中,我们建立了三个主要结果。首先,我们已经表明,G1 / S转型的年龄基本上决定出生率,表现出显着简单的缩放行为。除了从相当复杂的模型中出现这种简单行为的事实,这允许大量简化了我们的数值方法。另一个结果是观察到异质群体经历准中性竞争的内部过程。最后,我们研究了细胞周期相依赖性疗法(如放射治疗)对异质群体的影响。特别是,我们研究了人口含有静态子群的情况。我们的平均场分析和数值模拟证实,如果治疗的存活率太高,则会发生静态人群的救援。由于救助人口对治疗不太敏感,这导致对治疗的抵抗力产生。 (c)2016年作者。由elsevier有限公司出版。这是CC下的开放式访问文件。

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