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Global analysis of endothelial cell line proliferation patterns based on nutrient‐depletion models: implications for a standardization of cell proliferation assays

机译:基于营养耗竭模型的内皮细胞系增殖模式的全球分析:对细胞增殖测定法标准化的启示

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摘要

It is known that cell populations growing in different environmental conditions may exhibit different proliferation patterns. However, it is not clear if, despite the diversity of the so‐observed patterns, inherent cellular growth characteristics of the population can nevertheless be determined. This study quantifies the proliferative behaviour of the permanent endothelial human cell line, Eahy926, and establishes to which extent the estimation of the cell proliferation rate depends on variations of the experimental protocols. Cell proliferation curves were obtained for cells cultured over 16 days and the influences of cell seeding densities, foetal bovine serum content and frequency of culture medium changes were investigated. Quantitative dynamic modelling was conducted to evaluate the kinetic characteristics of this cell population. We proposed successive models and retained a nutrient‐depletion toxicity dependant model, which takes into account the progressive depletion of nutrients, as well as the increase of toxicity in the cell culture medium. This model is shown to provide a very good and robust prediction of the experimental proliferation curves, whatever are the considered frequency of culture medium changes and serum concentrations. Thus, the model enables an intrinsic quantification of the parameters driving EAhy926 proliferation, including proliferation, nutrient consumption and toxicity increase rates, rather independently of the experiments design. We therefore propose that such models could provide a basis for a standardized quantification of intrinsic cell proliferation kinetics.
机译:已知在不同环境条件下生长的细胞群体可能表现出不同的增殖方式。但是,尽管观察到的模式各不相同,但是尚不清楚是否可以确定人群固有的细胞生长特征。这项研究量化了永久性内皮人类细胞系Eahy926的增殖行为,并确定了细胞增殖率的估计取决于实验方案的不同程度。获得了16天培养的细胞的细胞增殖曲线,并研究了细胞接种密度,胎牛血清含量和培养基更换频率的影响。进行定量动力学建模以评估该细胞群体的动力学特征。我们提出了连续的模型,并保留了依赖营养物消耗的毒性模型,该模型考虑了营养物的逐步消耗以及细胞培养基中毒性的增加。无论考虑到培养基变化的频率和血清浓度如何,该模型均显示出对实验增殖曲线的很好而可靠的预测。因此,该模型能够对驱动EAhy926增殖的参数进行固有量化,包括增殖,养分消耗和毒性增加速率,而与实验设计无关。因此,我们建议这种模型可以为内在细胞增殖动力学的标准化量化提供基础。

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