血管网络三维建模的新方法

Maria Margarida Dias Soares Quinas Guerra, Rui D. M. Travasso
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引用次数: 6

摘要

模拟了一个混合多尺度相场模型,该模型描述了划分新毛细血管和基质的界面动力学。四个方程模拟了增殖内皮细胞(ECs)对促血管生成因子(T)梯度的响应行为,导致从原始毛细血管中萌芽的血管树的生长和时间进化。新的芽被激活的尖端细胞拉着,并以与血管生成因子梯度成正比的速度移动。促血管生成因子的来源是缺氧细胞。这个因子在整个三维系统中扩散,并被ec消耗,ec的扩散由一个序参数(φ)控制。趋化反应越高,血管分支数量增加,血管变薄;越厚的血管和分支网络的增殖率越高,缺氧细胞数量的增加导致分支数量越多,血管生成因子消耗越多,血管越长,内部的增殖能力越强。
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Novel approach to vascular network modeling in 3D
A simulation of a hybrid multi-scale phase-field model which describes the dynamics of the interface that divides the new capillaries and the stroma was performed. Four equations model the behaviour of proliferating endothelial cells (ECs) in response to a gradient of a pro-angiogenic factor (T), leading to the growth and time evolution of a tree of vascular vessels from sprouts emerging from the original capillar. New sprouts are pulled by activated tip cells and move with a velocity proportional to the gradient of angiogenic factors. The sources of pro-angiogenic factor are hypoxic cells. This factor diffuses throughout a three-dimensional system and is consumed by the ECs whose proliferation is governed by an order parameter (φ). Higher values of chemotactic response led to an increase of the number of ramifications in the vessels, which were thinner; higher values of proliferation rate to thicker vessels and a more ramified network and an increase in the number of hypoxic cells led to a higher number of branches, higher angiogenic factor consumption, longer and internally more proliferative vessels.
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