Monte Carlo simulation of cell death signaling predicts large cell-to-cell stochastic fluctuations through the type 2 pathway of apoptosis

被引:31
作者
Raychaudhuri, Subhadip [1 ,2 ,3 ,4 ]
Willgohs, Eric [1 ]
Nguyen, Thuc-Nghi [1 ]
Khan, Elaine M. [5 ]
Goldkorn, Tzipora [3 ,5 ]
机构
[1] Univ Calif Davis, Dept Biomed Engn, Davis, CA 95616 USA
[2] Univ Calif Davis, Grad Grp Biophys, Davis, CA 95616 USA
[3] Univ Calif Davis, Immunol Grad Grp, Davis, CA 95616 USA
[4] Univ Calif Davis, Grad Grp Appl Math, Davis, CA 95616 USA
[5] Univ Calif Davis, Sch Med, Davis, CA 95616 USA
关键词
D O I
10.1529/biophysj.108.135483
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
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 (similar to 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.
引用
收藏
页码:3559 / 3562
页数:4
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