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Confocal Imaging of Intercellular Calcium in HeLa Cells for Monitoring Drug-Response: Biophysical Framework for Visualization of the Time-Lapse Images

机译:HeLa细胞中细胞间钙的共聚焦成像以监测药物反应:时移图像的可视化的生物物理框架。

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Recent advancements in biomedical imaging focus on fluorescent imaging using laser scanning confocal microscopy. However, high-resolution imaging of cellular activity remains considerably expensive for both in vitro and in vivo model. In this context, integration of mathematical modeling and imaging data analysis to predict the cellular activity may aid understanding of cell signaling. Here we performed dynamic imaging using confocal microscopy and propose a model considering cell to cell connectivity that can predict the effect of the drug on Ca2+ oscillations. The proposed model consists of a large number of ordinary differential (ODE) equations and uses the concept of adjoint matrix containing coupling factors to capture the activity of cells with the random arrangement. The results show that the cell-to-cell connection plays a crucial role in controlling the calcium oscillations through a diffusion-based mechanism. The present simulation tool can be used as a generalized framework to generate and visualize the time-lapse videos required for in vitro drug testing for various drug doses.
机译:生物医学成像的最新进展集中在使用激光扫描共聚焦显微镜的荧光成像上。然而,对于体外和体内模型,细胞活性的高分辨率成像仍然相当昂贵。在这种情况下,数学建模和成像数据分析的集成以预测细胞活动可能有助于理解细胞信号传导。在这里,我们使用共聚焦显微镜进行了动态成像,并提出了一种考虑细胞间连通性的模型,该模型可以预测药物对钙的影响 2 + 振荡。所提出的模型由大量的常微分(ODE)方程组成,并使用包含耦合因子的伴随矩阵的概念来捕获具有随机排列的细胞的活动。结果表明,细胞间连接在通过基于扩散的机制控制钙振荡中起着至关重要的作用。本仿真工具可以用作通用框架,以生成和可视化各种药物剂量的体外药物测试所需的延时视频。

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