腺苷介导的血管生成算法模型的原理验证研究。

Q1 Mathematics
Francisco Azuaje, Frédérique Léonard, Magali Rolland-Turner, Yvan Devaux, Daniel R Wagner
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引用次数: 4

摘要

背景:我们研究了一种由血管内皮生长因子(VEGF)、抗血管生成可溶性VEGF受体1 (sVEGFR-1)和腺苷(Ado)控制的血管生成建模算法。我们探讨了其可行性,以测试血管生成相关的假设。我们通过增强VEGF活性和拮抗sVEGFR-1来研究Ado作为血管生成调节剂的作用。结果:我们实现了一个由内皮细胞、VEGF、sVEGFR-1和Ado实体的动态相互作用组成的血管生成算法模型。该模型基于一种基于逻辑规则的方法,其中细胞和分子的局部行为使用if-then规则进行编码。该模型显示了Ado分别通过激活和抑制VEGF和sVEGFR-1来促进血管生成。尽管该模型相对简单,但它概括了在体外模型中观察到的基本特征。然而,我们的模型和体外数据之间观察到的分歧表明可能存在知识差距,并可能指导未来的实验方向。结论:该模型可支持探索不同分子实体和实验条件在血管生成中的作用的假设。未来的扩展也可以应用于协助研究规划在这个和其他生物医学领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis.

Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis.

Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis.

Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis.

Background: We investigated an algorithmic approach to modelling angiogenesis controlled by vascular endothelial growth factor (VEGF), the anti-angiogenic soluble VEGF receptor 1 (sVEGFR-1) and adenosine (Ado). We explored its feasibility to test angiogenesis-relevant hypotheses. We illustrated its potential to investigate the role of Ado as an angiogenesis modulator by enhancing VEGF activity and antagonizing sVEGFR-1.

Results: We implemented an algorithmic model of angiogenesis consisting of the dynamic interaction of endothelial cells, VEGF, sVEGFR-1 and Ado entities. The model is based on a logic rule-based methodology in which the local behaviour of the cells and molecules is encoded using if-then rules. The model shows how Ado may enhance angiogenesis through activating and inhibiting effects on VEGF and sVEGFR-1 respectively. Despite the relative simplicity of the model, it recapitulated basic features observed in in vitro models. However, observed disagreements between our models and in vitro data suggest possible knowledge gaps and may guide future experimental directions.

Conclusions: The proposed model can support the exploration of hypotheses about the role of different molecular entities and experimental conditions in angiogenesis. Future expansions can also be applied to assist research planning in this and other biomedical domains.

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来源期刊
Theoretical Biology and Medical Modelling
Theoretical Biology and Medical Modelling MATHEMATICAL & COMPUTATIONAL BIOLOGY-
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Theoretical Biology and Medical Modelling is an open access peer-reviewed journal adopting a broad definition of "biology" and focusing on theoretical ideas and models associated with developments in biology and medicine. Mathematicians, biologists and clinicians of various specialisms, philosophers and historians of science are all contributing to the emergence of novel concepts in an age of systems biology, bioinformatics and computer modelling. This is the field in which Theoretical Biology and Medical Modelling operates. We welcome submissions that are technically sound and offering either improved understanding in biology and medicine or progress in theory or method.
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