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Monte Carlo Simulation of Cell Death Signaling Predicts Large Cell-to-Cell Stochastic Fluctuations through the Type 2 Pathway of Apoptosis

机译:细胞死亡信号的蒙特卡洛模拟预测通过细胞凋亡的2型途径大细胞间的随机波动。

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摘要

Apoptosis, or genetically programmed cell death, is a crucial cellular process that maintains the balance between life and death in cells. The precise molecular mechanism of apoptosis signaling and the manner in which type 1 and type 2 pathways of the apoptosis signaling network are differentially activated under distinct apoptotic stimuli is poorly understood. Based on Monte Carlo stochastic simulations, we show that the type 1 pathway becomes activated under strong apoptotic stimuli, whereas the type 2 mitochondrial pathway dominates apoptotic signaling in response to a weak death signal. Our results also show signaling in the type 2 pathway is stochastic; the population average over many cells does not capture the cell-to-cell fluctuations in the time course (∼1–10 h) of downstream caspase-3 activation. On the contrary, the probability distribution of caspase-3 activation for the mitochondrial pathway shows a distinct bimodal behavior that can be used to characterize the stochastic signaling in type 2 apoptosis and other similar complex signaling processes. Interestingly, such stochastic fluctuations in apoptosis signaling occur even in the presence of large numbers of signaling molecules.
机译:凋亡或基因编程的细胞死亡是维持细胞生命与死亡之间平衡的关键细胞过程。人们对细胞凋亡信号传导的确切分子机制以及细胞凋亡信号传导网络的1型和2型途径在不同的凋亡刺激下被差异激活的方式了解甚少。基于蒙特卡洛随机模拟,我们显示1型途径在强烈的细胞凋亡刺激下被激活,而2型线粒体途径在对微弱死亡信号的响应中主导细胞凋亡信号。我们的结果还表明2型途径中的信号是随机的。在下游caspase-3激活的时间过程(约1-10小时)中,许多细胞的平均数并未捕获细胞间的波动。相反,线粒体途径中caspase-3激活的概率分布显示出独特的双峰行为,可用于表征2型细胞凋亡和其他类似复杂信号过程中的随机信号。有趣的是,即使存在大量的信号分子,细胞凋亡信号的这种随机波动也会发生。

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