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一种用于模拟细胞群体中异质钙反应的贝叶斯方法。

A Bayesian approach to modelling heterogeneous calcium responses in cell populations.

作者信息

Tilūnaitė Agne, Croft Wayne, Russell Noah, Bellamy Tomas C, Thul Rüdiger

机构信息

School of Mathematical Sciences, University of Nottingham, Nottingham, England, United Kingdom.

School of Life Sciences, University of Nottingham, Nottingham, England, United Kingdom.

出版信息

PLoS Comput Biol. 2017 Oct 6;13(10):e1005794. doi: 10.1371/journal.pcbi.1005794. eCollection 2017 Oct.

Abstract

Calcium responses have been observed as spikes of the whole-cell calcium concentration in numerous cell types and are essential for translating extracellular stimuli into cellular responses. While there are several suggestions for how this encoding is achieved, we still lack a comprehensive theory. To achieve this goal it is necessary to reliably predict the temporal evolution of calcium spike sequences for a given stimulus. Here, we propose a modelling framework that allows us to quantitatively describe the timing of calcium spikes. Using a Bayesian approach, we show that Gaussian processes model calcium spike rates with high fidelity and perform better than standard tools such as peri-stimulus time histograms and kernel smoothing. We employ our modelling concept to analyse calcium spike sequences from dynamically-stimulated HEK293T cells. Under these conditions, different cells often experience diverse stimulus time courses, which is a situation likely to occur in vivo. This single cell variability and the concomitant small number of calcium spikes per cell pose a significant modelling challenge, but we demonstrate that Gaussian processes can successfully describe calcium spike rates in these circumstances. Our results therefore pave the way towards a statistical description of heterogeneous calcium oscillations in a dynamic environment.

摘要

在众多细胞类型中,钙反应已被观察为全细胞钙浓度的峰值,并且对于将细胞外刺激转化为细胞反应至关重要。虽然对于如何实现这种编码有几种建议,但我们仍然缺乏一个全面的理论。为了实现这一目标,有必要可靠地预测给定刺激下钙峰值序列的时间演变。在这里,我们提出了一个建模框架,使我们能够定量描述钙峰值的时间。使用贝叶斯方法,我们表明高斯过程能够以高保真度对钙峰值速率进行建模,并且比诸如刺激周围时间直方图和核平滑等标准工具表现更好。我们运用我们的建模概念来分析动态刺激的HEK293T细胞的钙峰值序列。在这些条件下,不同的细胞通常会经历不同的刺激时间进程,这是一种在体内可能发生的情况。这种单细胞变异性以及每个细胞伴随的少量钙峰值构成了一个重大的建模挑战,但我们证明高斯过程能够在这些情况下成功描述钙峰值速率。因此,我们的结果为动态环境中异质钙振荡的统计描述铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3009/5646906/ed396f04fe45/pcbi.1005794.g001.jpg

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