Lyapunov exponents and phase diagrams reveal multi-factorial control over TRAIL-induced apoptosis

被引:46
作者
Aldridge, Bree B. [1 ,2 ]
Gaudet, Suzanne [1 ]
Lauffenburger, Douglas A. [2 ]
Sorger, Peter K. [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Dept Syst Biol, Ctr Cell Decis Proc, Boston, MA 02115 USA
[2] MIT, Dept Biol Engn, Ctr Cell Decis Proc, Cambridge, MA 02139 USA
关键词
apoptosis; caspases; dynamical systems analysis; kinetic modeling; XIAP; X-LINKED INHIBITOR; RECEPTOR-INDUCED APOPTOSIS; CD95; TYPE-I; CASPASE ACTIVATION; XIAP INHIBITION; PROTEIN XIAP; CELL-DEATH; INACTIVATION; DEGRADATION; SMAC/DIABLO;
D O I
10.1038/msb.2011.85
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Receptor-mediated apoptosis proceeds via two pathways: one requiring only a cascade of initiator and effector caspases (type I behavior) and the second requiring an initiator-effector caspase cascade and mitochondrial outer membrane permeabilization (type II behavior). Here, we investigate factors controlling type I versus II phenotypes by performing Lyapunov exponent analysis of an ODE-based model of cell death. The resulting phase diagrams predict that the ratio of XIAP to pro-caspase-3 concentrations plays a key regulatory role: type I behavior predominates when the ratio is low and type II behavior when the ratio is high. Cell-to-cell variability in phenotype is observed when the ratio is close to the type I versus II boundary. By positioning multiple tumor cell lines on the phase diagram we confirm these predictions. We also extend phase space analysis to mutations affecting the rate of caspase-3 ubiquitylation by XIAP, predicting and showing that such mutations abolish all-or-none control over activation of effector caspases. Thus, phase diagrams derived from Lyapunov exponent analysis represent a means to study multi-factorial control over a complex biochemical pathway. Molecular Systems Biology 7: 553; published online 22 November 2011; doi:10.1038/msb.2011.85
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页数:21
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