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

被引:301
|
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
相关论文
共 50 条
  • [1] A single NFκB system for both canonical and non-canonical signaling
    Vincent Feng-Sheng Shih
    Rachel Tsui
    Andrew Caldwell
    Alexander Hoffmann
    Cell Research, 2011, 21 : 86 - 102
  • [2] Copper is a potent inhibitor of both the canonical and non-canonical NFκB pathways
    Kenneth, Niall S.
    Hucks, George E., Jr.
    Kocab, Andrew J.
    McCollom, Annie L.
    Duckett, Colin S.
    CELL CYCLE, 2014, 13 (06) : 1006 - 1014
  • [3] Non-canonical NF-κB signaling pathway
    Shao-Cong Sun
    Cell Research, 2011, 21 : 71 - 85
  • [4] Non-canonical NF-κB signaling pathway
    Sun, Shao-Cong
    CELL RESEARCH, 2011, 21 (01) : 71 - 85
  • [5] Restricting non-canonical NFκB
    Andrea Du Toit
    Nature Reviews Molecular Cell Biology, 2014, 15 (3) : 151 - 151
  • [6] Canonical and Non-canonical Reelin Signaling
    Bock, Hans H.
    May, Petra
    FRONTIERS IN CELLULAR NEUROSCIENCE, 2016, 10
  • [7] Constitutive non-canonical NFκB signaling in pancreatic cancer cells
    Wharry, Catherine E.
    Haines, Kathleen M.
    Carroll, Richard G.
    May, Michael J.
    CANCER BIOLOGY & THERAPY, 2009, 8 (16) : 1567 - 1576
  • [8] Manipulation of Non-canonical NF-B Signaling by Non-oncogenic Viruses
    Struzik, Justyna
    Szulc-Dabrowska, Lidia
    ARCHIVUM IMMUNOLOGIAE ET THERAPIAE EXPERIMENTALIS, 2019, 67 (01) : 41 - 48
  • [9] Non-canonical NF-κB signaling activation and regulation: principles and perspectives
    Razani, Bahram
    Reichardt, Anna Devi
    Cheng, Genhong
    IMMUNOLOGICAL REVIEWS, 2011, 244 : 44 - 54
  • [10] NON-CANONICAL NF-κB SIGNALING DRIVES THE AGGRESSIVE INVASIVENESS OF GLIOBLASTOMA
    Cherry, Evan
    Lee, Dong
    Jung, Jiung
    Sitcheran, Raquel
    NEURO-ONCOLOGY, 2014, 16