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2D data-driven stalk cell prediction model based on tip-stalk cell interaction in angiogenesis

机译:基于尖端茎细胞相互作用的二维数据驱动茎细胞预测模型

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Angiogenesis is the growth process of blood vessels from existing vessels. During angiogenesis, endothelial cells (ECs), which line the vessel, specialize into tip and stalk cells. Tip cells respond to angiogenic signals, burrow into the extracellular matrix (ECM) and form conduits. Stalk cells follow the tip cells along the conduits, and form solid sprouts or lumen vessels. Interactions between stalk cells and tip cells are important for creating functional vessels. The goal of this work is to predict stalk cells migration trajectories from known tip cell trajectories. Four factors influence the position and velocity of cell migration in ECM: cell-cell interaction, drag force, chemotactic signal and cell-ECM interaction. As chemotactic signal and cell-ECM interactions have little effect on stalk cell movement, the proposed model includes the influence of cell-cell interactions and drag force only. The unknown parameters in the model are inferred by Maximum Likelihood Estimation (MLE) from experimental time-lapse cell migration data. Numerical results suggest that the proposed model can accurately predict stalk cell trajectories. The proposed model may be useful for the study of angiogenesis, a critical process for cancer tumor growth.
机译:血管生成是现有血管中血管的生长过程。在血管生成过程中,位于血管内的内皮细胞(EC)专长于尖端和茎细胞。尖端细胞响应血管生成信号,钻入细胞外基质(ECM)并形成导管。茎细胞沿着导管沿着尖端细胞,并形成固体芽或腔管。茎细胞和尖端细胞之间的相互作用对于创建功能性血管很重要。这项工作的目的是根据已知的尖端细胞轨迹预测茎细胞的迁移轨迹。四个因素影响ECM中细胞迁移的位置和速度:细胞-细胞相互作用,拖曳力,趋化信号和细胞-ECM相互作用。由于趋化信号和细胞-ECM相互作用对茎细胞的运动影响很小,因此该模型仅包括细胞-细胞相互作用和阻力的影响。通过实验时移细胞迁移数据的最大似然估计(MLE)推断模型中的未知参数。数值结果表明,该模型可以准确预测茎细胞的轨迹。所提出的模型可能对血管生成的研究有用,血管生成是癌症肿瘤生长的关键过程。

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