A Systems Model of Signaling Identifies a Molecular Basis Set for Cytokine-Induced Apoptosis 论文

2005Science引用 541
Computational Drug Discovery MethodsReceptor Mechanisms and SignalingProtein Kinase Regulation and GTPase Signaling

详细信息

发表期刊/会议
Science
发表日期
2005-12-08
发表年份
2005

关键词

Computational Drug Discovery MethodsReceptor Mechanisms and SignalingProtein Kinase Regulation and GTPase Signaling

摘要

Signal transduction pathways control cellular responses to stimuli, but it is unclear how molecular information is processed as a network. We constructed a systems model of 7980 intracellular signaling events that directly links measurements to 1440 response outputs associated with apoptosis. The model accurately predicted multiple time-dependent apoptotic responses induced by a combination of the death-inducing cytokine tumor necrosis factor with the prosurvival factors epidermal growth factor and insulin. By capturing the role of unsuspected autocrine circuits activated by transforming growth factor-alpha and interleukin-1alpha, the model revealed new molecular mechanisms connecting signaling to apoptosis. The model derived two groupings of intracellular signals that constitute fundamental dimensions (molecular "basis axes") within the apoptotic signaling network. Projection along these axes captures the entire measured apoptotic network, suggesting that cell survival is determined by signaling through this canonical basis set.