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Agent-based model of angiogenesis simulates capillary sprout initiation in multicellular networks

机译:基于代理的血管生成模型模拟多细胞网络中的毛细血管萌芽

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摘要

Many biological processes are controlled by both deterministic and stochastic influences. However, efforts to model these systems often rely on either purely stochastic or purely rule-based methods. To better understand the balance between stochasticity and determinism in biological processes a computational approach that incorporates both influences may afford additional insight into underlying biological mechanisms that give rise to emergent system properties. We apply a combined approach to the simulation and study of angiogenesis, the growth of new blood vessels from existing networks. This complex multicellular process begins with selection of an initiating endothelial cell, or tip cell, which sprouts from the parent vessels in response to stimulation by exogenous cues. We have constructed an agent-based model of sprouting angiogenesis to evaluate endothelial cell sprout initiation frequency and location, and we have experimentally validated it using high-resolution time-lapse confocal microscopy. ABM simulations were then compared to a Monte Carlo model, revealing that purely stochastic simulations could not generate sprout locations as accurately as the rule-informed agent-based model. These findings support the use of rule-based approaches for modeling the complex mechanisms underlying sprouting angiogenesis over purely stochastic methods.
机译:许多生物过程都受到确定性和随机性影响的控制。但是,对这些系统进行建模的工作通常依赖于纯粹随机的或纯粹基于规则的方法。为了更好地理解生物过程中随机性和确定性之间的平衡,结合了这两种影响的计算方法可以提供对引起新兴系统特性的潜在生物学机制的进一步了解。我们将组合方法应用于模拟和研究血管生成,即现有网络中新血管的生长。这种复杂的多细胞过程始于选择起始内皮细胞或尖端细胞,该内皮细胞或尖端细胞响应于外源线索的刺激而从亲本血管中萌芽。我们已经建立了一个基于代理的发芽血管生成模型来评估内皮细胞发芽的起始频率和位置,并且我们已经使用高分辨率时移共聚焦显微镜对它进行了实验验证。然后将ABM模拟与蒙特卡洛模型进行比较,发现纯随机模拟无法像基于规则的基于主体的模型那样准确地生成萌芽位置。这些发现支持使用基于规则的方法对纯随机方法之上发芽血管生成的复杂机制进行建模。

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