A single NFκB system for both canonical and non-canonical signaling

被引:300
作者
Shih, Vincent Feng-Sheng [1 ,2 ]
Tsui, Rachel [1 ,2 ]
Caldwell, Andrew [1 ,2 ]
Hoffmann, Alexander [1 ,2 ]
机构
[1] Univ Calif San Diego, Signaling Syst Lab, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Chem & Biochem, San Diego Ctr Syst Biol, La Jolla, CA 92093 USA
关键词
NF kappa B; inflammation; immune response; immune development; mathematical model; signaling crosstalk; LYMPHOID ORGAN DEVELOPMENT; SELECTIVE GENE ACTIVATION; SEVERE LIVER DEGENERATION; DEFICIENT MICE; IKK-ALPHA; C-REL; TRANSCRIPTION FACTORS; TNF-ALPHA; TEMPORAL CONTROL; SPLENIC MICROARCHITECTURE;
D O I
10.1038/cr.2010.161
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Two distinct nuclear factor kappa B (NF kappa B) signaling pathways have been described; the canonical pathway that mediates inflammatory responses, and the non-canonical pathway that is involved in immune cell differentiation and maturation and secondary lymphoid organogenesis. The former is dependent on the I kappa B kinase adaptor molecule NEMO, the latter is independent of it. Here, we review the molecular mechanisms of regulation in each signaling axis and attempt to relate the apparent regulatory logic to the physiological function. Further, we review the recent evidence for extensive cross-regulation between these two signaling axes and summarize them in a wiring diagram. These observations suggest that NEMO-dependent and -independent signaling should be viewed within the context of a single NF kappa B signaling system, which mediates signaling from both inflammatory and organogenic stimuli in an integrated manner. As in other regulatory biological systems, a systems approach including mathematical models that include quantitative and kinetic information will be necessary to characterize the network properties that mediate physiological function, and that may break down to cause or contribute to pathology.
引用
收藏
页码:86 / 102
页数:17
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