Circuitry of nuclear factor κB signaling

被引:756
作者
Hoffmann, A
Baltimore, D
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, Signaling Syst Lab, La Jolla, CA 92093 USA
[2] CALTECH, Div Biol, Pasadena, CA 91125 USA
关键词
D O I
10.1111/j.0105-2896.2006.00375.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
Over the past few years, the transcription factor nuclear factor (NF)-kappa B and the proteins that regulate it have emerged as a signaling system of pre-eminent importance in human physiology and in an increasing number of pathologies. While NF-kappa B is present in all differentiated cell types, its discovery and early characterization were rooted in understanding B-cell biology. Significant research efforts over two decades have yielded a large body of literature devoted to understanding NF-kappa B's functioning in the immune system. NF-kappa B has been found to play roles in many different compartments of the immune system during differentiation of immune cells and development of lymphoid organs and during immune activation. NF-kappa B is the nuclear effector of signaling pathways emanating from many receptors, including those of the inflammatory tumor necrosis factor and Toll-like receptor superfamilies. With this review, we hope to provide historical context and summarize the diverse physiological functions of NF-kappa B in the immune system before focusing on recent advances in elucidating the molecular mechanisms that mediate cell type-specific and stimulus-specific functions of this pleiotropic signaling system. Understanding the genetic regulatory circuitry of NF-kappa B functionalities involves system-wide measurements, biophysical studies, and computational modeling.
引用
收藏
页码:171 / 186
页数:16
相关论文
共 93 条
  • [21] Induction of gadd45β by NF-κB downregulates pro-apoptotic JNK signalling
    De Smaele, E
    Zazzeroni, F
    Papa, S
    Nguyen, DU
    Jin, RG
    Jones, J
    Cong, R
    Franzoso, G
    [J]. NATURE, 2001, 414 (6861) : 308 - 313
  • [22] The lymphotoxin-β receptor induces different patterns of gene expression via two NF-κB pathways
    Dejardin, E
    Droin, NM
    Delhase, M
    Haas, E
    Cao, YX
    Makris, C
    Li, ZW
    Karin, M
    Ware, CF
    Green, DR
    [J]. IMMUNITY, 2002, 17 (04) : 525 - 535
  • [23] A cytokine-responsive I kappa B kinase that activates the transcription factor NF-kappa B
    DiDonato, JA
    Hayakawa, M
    Rothwarf, DM
    Zandi, E
    Karin, M
    [J]. NATURE, 1997, 388 (6642) : 548 - 554
  • [24] THE CANDIDATE PROTOONCOGENE BCL-3 ENCODES A TRANSCRIPTIONAL COACTIVATOR THAT ACTIVATES THROUGH NF-KAPPA-B P50 HOMODIMERS
    FUJITA, T
    NOLAN, GP
    LIOU, HC
    SCOTT, ML
    BALTIMORE, D
    [J]. GENES & DEVELOPMENT, 1993, 7 (7B) : 1354 - 1363
  • [25] Genetic approaches in mice to understand Rel/NF-κB and IκB function:: transgenics and knockouts
    Gerondakis, S
    Grossmann, M
    Nakamura, Y
    Pohl, T
    Grumont, R
    [J]. ONCOGENE, 1999, 18 (49) : 6888 - 6895
  • [26] The role of Rel/NF-κB transcription factors in B lymphocyte survival
    Gerondakis, S
    Strasser, A
    [J]. SEMINARS IN IMMUNOLOGY, 2003, 15 (03) : 159 - 166
  • [27] CLONING OF THE P50 DNA-BINDING SUBUNIT OF NF-KAPPA-B - HOMOLOGY TO REL AND DORSAL
    GHOSH, S
    GIFFORD, AM
    RIVIERE, LR
    TEMPST, P
    NOLAN, GP
    BALTIMORE, D
    [J]. CELL, 1990, 62 (05) : 1019 - 1029
  • [28] Rel-dependent induction of A1 transcription is required to protect B cells from antigen receptor ligation-induced apoptosis
    Grumont, RJ
    Rourke, IJ
    Gerondakis, S
    [J]. GENES & DEVELOPMENT, 1999, 13 (04) : 400 - 411
  • [29] Limiting inflammatory responses during activation of innate immunity
    Han, JH
    Ulevitch, RJ
    [J]. NATURE IMMUNOLOGY, 2005, 6 (12) : 1198 - 1205
  • [30] Hinz M, 1999, MOL CELL BIOL, V19, P2690