Dynamics within the CD95 death-inducing signaling complex decide life and death of cells

被引:109
|
作者
Neumann, Leo [1 ,4 ]
Pforr, Carina [2 ]
Beaudouin, Joel [1 ,4 ]
Pappa, Alexander [2 ,3 ]
Fricker, Nicolai [2 ]
Krammer, Peter H. [2 ]
Lavrik, Inna N. [2 ]
Eils, Roland [1 ,4 ]
机构
[1] German Canc Res Ctr, Div Theoret Bioinformat, D-69120 Heidelberg, Germany
[2] German Canc Res Ctr, Div Immunogenet, D-69120 Heidelberg, Germany
[3] Medac GmbH, Wedel Hamburg, Germany
[4] Univ Heidelberg, Inst Pharm & Mol Biotechnol, Dept Bioinformat & Funct Genom, Heidelberg, Germany
关键词
apoptosis; CD95; signaling; DISC; model reduction; NF-kappa B; NF-KAPPA-B; RECEPTOR-INDUCED APOPTOSIS; CASPASE-8; ACTIVATION; CD95-INDUCED APOPTOSIS; LONG FORM; T-CELLS; C-FLIPL; INHIBITOR; MODEL; FADD;
D O I
10.1038/msb.2010.6
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
This study explores the dilemma in cellular signaling that triggering of CD95 (Fas/APO-1) in some situations results in cell death and in others leads to the activation of NF-kappa B. We established an integrated kinetic mathematical model for CD95-mediated apoptotic and NF-kappa B signaling. Systematic model reduction resulted in a surprisingly simple model well approximating experimentally observed dynamics. The model postulates a new link between c-FLIPL cleavage in the death-inducing signaling complex (DISC) and the NF-kappa B pathway. We validated experimentally that CD95 stimulation resulted in an interaction of p43-FLIP with the IKK complex followed by its activation. Furthermore, we showed that the apoptotic and NF-kappa B pathways diverge already at the DISC. Model and experimental analysis of DISC formation showed that a subtle balance of c-FLIPL and procaspase-8 determines life/death decisions in a nonlinear manner. We present an integrated model describing the complex dynamics of CD95-mediated apoptosis and NF-kappa B signaling. Molecular Systems Biology 6: published online 9 March 2010; doi: 10.1038/msb.2010.6
引用
收藏
页数:17
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