Lessons from mathematically modeling the NF-κB pathway

被引:104
作者
Basak, Soumen [2 ]
Behar, Marcelo [1 ]
Hoffmann, Alexander [1 ]
机构
[1] Univ Calif San Diego, San Diego Ctr Syst Biol Cellular Stress Responses, Signaling Syst Lab, La Jolla, CA 92093 USA
[2] Natl Inst Immunol, Syst Immunol Lab, New Delhi 110067, India
基金
英国惠康基金;
关键词
computational models; I?B control; temporal control; signaling dynamics; dose-response control; negative feedback; LYMPHOTOXIN BETA-RECEPTOR; TUMOR-NECROSIS-FACTOR; TO-CELL VARIABILITY; GENE-EXPRESSION; TEMPORAL CONTROL; INDEPENDENT DEGRADATION; INFLAMMATORY RESPONSE; TRANSCRIPTION FACTORS; SENSITIVITY-ANALYSIS; SIGNALING PATHWAY;
D O I
10.1111/j.1600-065X.2011.01092.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mathematical modeling has proved to be a critically important approach in the study of many complex networks and dynamic systems in physics, engineering, chemistry, and biology. The nuclear factor ?B (NF-?B) system consists of more than 50 proteins and protein complexes and is both a highly networked and dynamic system. To date, mathematical modeling has only addressed a small fraction of the molecular species and their regulation, but when employed in conjunction with experimental analysis has already led to important insights. Here, we provide a personal account of studying how the NF-?B signaling system functions using mathematical descriptions of the molecular mechanisms. We focus on the insights gained about some of the key regulatory components: the control of the steady state, the signaling dynamics, and signaling crosstalk. We also discuss the biological relevance of these regulatory systems properties.
引用
收藏
页码:221 / 238
页数:18
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