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
相关论文
共 67 条
[11]   Understanding NF-κB signaling via mathematical modeling [J].
Cheong, Raymond ;
Hoffmann, Alexander ;
Levchenko, Andre .
MOLECULAR SYSTEMS BIOLOGY, 2008, 4 (1)
[12]   Hodgkin lymphoma cells express TACI and BCMA receptors and generate survival and proliferation signals in response to BAFF and APRIL [J].
Chiu, April ;
Xu, Weifeng ;
He, Bing ;
Dillon, Stacey R. ;
Gross, Jane A. ;
Sievers, Eric ;
Qiao, Xugang ;
Santini, Paul ;
Hyjek, Elizabeth ;
Lee, Joong-Won ;
Cesarman, Ethel ;
Chadburn, Amy ;
Knowles, Daniel M. ;
Cerutti, Andrea .
BLOOD, 2007, 109 (02) :729-739
[13]   Investigations into the analysis and modeling of the TNFα-mediated NF-κB-signaling pathway [J].
Cho, KH ;
Shin, SY ;
Lee, HW ;
Wolkenhauer, O .
GENOME RESEARCH, 2003, 13 (11) :2413-2422
[14]   Achieving stability of lipopolysaccharide-induced NF-κB activation [J].
Covert, MW ;
Leung, TH ;
Gaston, JE ;
Baltimore, D .
SCIENCE, 2005, 309 (5742) :1854-1857
[15]   Regulation of p100 (NFKB2) expression in human monocytes in response to inflammatory mediators and lymphokines [J].
de Wit, H ;
Dokter, WHA ;
Koopmans, SB ;
Lummen, C ;
van der Leij, M ;
Smit, JW ;
Vellenga, E .
LEUKEMIA, 1998, 12 (03) :363-370
[16]   The lymphotoxin β receptor controls organogenesis and affinity maturation in peripheral lymphoid tissues [J].
Fütterer, A ;
Mink, K ;
Luz, A ;
Kosco-Vilbois, MH ;
Pfeffer, K .
IMMUNITY, 1998, 9 (01) :59-70
[17]   New regulators of NF-κB in inflammation [J].
Ghosh, Sankar ;
Hayden, Matthew S. .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (11) :837-848
[18]   Noncooperative Interactions between Transcription Factors and Clustered DNA Binding Sites Enable Graded Transcriptional Responses to Environmental Inputs [J].
Giorgetti, Luca ;
Siggers, Trevor ;
Tiana, Guido ;
Caprara, Greta ;
Notarbartolo, Samuele ;
Corona, Teresa ;
Pasparakis, Manolis ;
Milani, Paolo ;
Bulyk, Martha L. ;
Natoli, Gioacchino .
MOLECULAR CELL, 2010, 37 (03) :418-428
[19]   Mathematical modeling identified c-FLIP as an apoptotic switch in death receptor induced apoptosis [J].
Han, Lihui ;
Zhao, Yishu ;
Jia, Xiaoqing .
APOPTOSIS, 2008, 13 (10) :1198-1204
[20]   NF-κB oscillations and cell-to-cell variability [J].
Hayot, F. ;
Jayaprakash, C. .
JOURNAL OF THEORETICAL BIOLOGY, 2006, 240 (04) :583-591