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Calibrating spatio-temporal models of leukocyte dynamics against in vivo live-imaging data using approximate Bayesian computation

机译:使用近似贝叶斯计算,针对体内实时成像数据校准白细胞动力学的时空模型

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摘要

In vivo studies allow us to investigate biological processes at the level of the organism. But not all aspects of in vivo systems are amenable to direct experimental measurements. In order to make the most of such data we therefore require statistical tools that allow us to obtain reliable estimates for e. g. kinetic in vivo parameters. Here we show how we can use approximate Bayesian computation approaches in order to analyse leukocyte migration in zebrafish embryos in response to injuries. We track individual leukocytes using live imaging following surgical injury to the embryos' tail-fins. The signalling gradient that leukocytes follow towards the site of the injury cannot be directly measured but we can estimate its shape and how it changes with time from the directly observed patterns of leukocyte migration. By coupling simple models of immune signalling and leukocyte migration with the unknown gradient shape into a single statistical framework we can gain detailed insights into the tissue-wide processes that are involved in the innate immune response to wound injury. In particular we find conclusive evidence for a temporally and spatially changing signalling gradient that modulates the changing activity of the leukocyte population in the embryos. We conclude with a robustness analysis which highlights the most important factors determining the leukocyte dynamics. Our approach relies only on the ability to simulate numerically the process under investigation and is therefore also applicable in other in vivo contexts and studies.
机译:体内研究使我们能够在生物体水平上研究生物学过程。但是,并非体内系统的所有方面都适合直接进行实验测量。因此,为了充分利用这些数据,我们需要统计工具,以使我们能够获得e的可靠估计。 G。体内动力学参数。在这里,我们展示了如何使用近似贝叶斯计算方法来分析斑马鱼胚胎中白细胞迁移对伤害的反应。在对胚胎尾鳍进行手术损伤后,我们使用实时成像追踪单个白细胞。无法直接测量白细胞朝向损伤部位的信号传导梯度,但是我们可以从直接观察到的白细胞迁移模式中估计其形状以及其随时间的变化。通过将免疫信号和白细胞迁移的简单模型与未知的梯度形状耦合到一个统计框架中,我们可以获得对涉及伤口损伤的先天免疫反应所涉及的整个组织过程的详细见解。特别是,我们找到了确定信号的时空变化的确凿证据,该信号梯度可调节胚胎中白细胞种群的变化活性。我们以鲁棒性分析结束,该鲁棒性分析突出了决定白细胞动力学的最重要因素。我们的方法仅依赖于对所研究过程进行数值模拟的能力,因此也适用于其他体内环境和研究。

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