Martinson W Duncan, Volkening Alexandria, Schmidtchen Markus, Venkataraman Chandrasekhar, Carrillo José A
Mathematical Institute, University of Oxford, Oxford, UK.
Department of Mathematics, Purdue University, West Lafayette, IN, USA.
R Soc Open Sci. 2024 Jul 17;11(7):232002. doi: 10.1098/rsos.232002. eCollection 2024 Jul.
Self-organization of individuals within large collectives occurs throughout biology. Mathematical models can help elucidate the individual-level mechanisms behind these dynamics, but analytical tractability often comes at the cost of biological intuition. Discrete models provide straightforward interpretations by tracking each individual yet can be computationally expensive. Alternatively, continuous models supply a large-scale perspective by representing the 'effective' dynamics of infinite agents, but their results are often difficult to translate into experimentally relevant insights. We address this challenge by quantitatively linking spatio-temporal dynamics of continuous models and individual-based data in settings with biologically realistic, time-varying cell numbers. Specifically, we introduce and fit scaling parameters in continuous models to account for discrepancies that can arise from low cell numbers and localized interactions. We illustrate our approach on an example motivated by zebrafish-skin pattern formation, in which we create a continuous framework describing the movement and proliferation of a single cell population by upscaling rules from a discrete model. Our resulting continuous models accurately depict ensemble average agent-based solutions when migration or proliferation act alone. Interestingly, the same parameters are not optimal when both processes act simultaneously, highlighting a rich difference in how combining migration and proliferation affects discrete and continuous dynamics.
个体在大型群体中的自组织现象在整个生物学领域都有发生。数学模型有助于阐明这些动态背后的个体层面机制,但解析的易处理性往往是以牺牲生物学直觉为代价的。离散模型通过追踪每个个体提供了直接的解释,但计算成本可能很高。相比之下,连续模型通过表示无限个体的“有效”动态提供了大规模视角,但其结果往往难以转化为与实验相关的见解。我们通过在具有生物学现实意义、随时间变化的细胞数量的环境中,定量地将连续模型的时空动态与基于个体的数据联系起来,来应对这一挑战。具体而言,我们在连续模型中引入并拟合缩放参数,以解释因细胞数量少和局部相互作用而可能出现的差异。我们以斑马鱼皮肤图案形成为例来说明我们的方法,在这个例子中,我们通过放大离散模型的规则,创建了一个描述单个细胞群体运动和增殖的连续框架。当迁移或增殖单独起作用时,我们得到的连续模型准确地描绘了基于个体的总体平均解。有趣的是,当这两个过程同时起作用时,相同的参数并非最优,这突出了迁移和增殖相结合对离散和连续动态影响方式的丰富差异。