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Sci. STKE, 17 October 2006
Vol. 2006, Issue 357, p. re13
[DOI: 10.1126/stke.3572006re13]
REVIEWS
Regulation and Function of IKK and IKK-Related Kinases
Hans Häcker1* and
Michael Karin2
1Department of Infectious Diseases, St. Jude Children's Research Hospital, 332 North Lauderdale Street, Memphis, TN 38105, USA. 2Laboratory of Gene Regulation and Signal Transduction, Department of Pharmacology, School of Medicine, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Abstract:
Members of the nuclear factor kappa B (NF-B) family of dimeric transcription factors (TFs) regulate expression of a large number of genes involved in immune responses, inflammation, cell survival, and cancer. NF-B TFs are rapidly activated in response to various stimuli, including cytokines, infectious agents, and radiation-induced DNA double-strand breaks. In nonstimulated cells, some NF-B TFs are bound to inhibitory IB proteins and are thereby sequestered in the cytoplasm. Activation leads to phosphorylation of IB proteins and their subsequent recognition by ubiquitinating enzymes. The resulting proteasomal degradation of IB proteins liberates IB-bound NF-B TFs, which translocate to the nucleus to drive expression of target genes. Two protein kinases with a high degree of sequence similarity, IKK and IKK, mediate phosphorylation of IB proteins and represent a convergence point for most signal transduction pathways leading to NF-B activation. Most of the IKK and IKK molecules in the cell are part of IKK complexes that also contain a regulatory subunit called IKK or NEMO. Despite extensive sequence similarity, IKK and IKK have largely distinct functions, due to their different substrate specificities and modes of regulation. IKK (and IKK) are essential for rapid NF-B activation by proinflammatory signaling cascades, such as those triggered by tumor necrosis factor (TNF) or lipopolysaccharide (LPS). In contrast, IKK functions in the activation of a specific form of NF-B in response to a subset of TNF family members and may also serve to attenuate IKK-driven NF-B activation. Moreover, IKK is involved in keratinocyte differentiation, but this function is independent of its kinase activity. Several years ago, two protein kinases, one called IKK or IKK-i and one variously named TBK1 (TANK-binding kinase), NAK (NF-Bactivated kinase), or T2K (TRAF2-associated kinase), were identified that exhibit structural similarity to IKK and IKK. These protein kinases are important for the activation of interferon response factor 3 (IRF3) and IRF7, TFs that play key roles in the induction of type I interferon (IFN-I). Together, the IKKs and IKK-related kinases are instrumental for activation of the host defense system. This Review focuses on the functions of IKK and IKK-related kinases and the molecular mechanisms that regulate their activities.
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Site-Specific Antiatherogenic Effect of the Antioxidant Ebselen in the Diabetic Apolipoprotein E-Deficient Mouse.
P. Chew, D. Y.C. Yuen, P. Koh, N. Stefanovic, M. A. Febbraio, I. Kola, M. E. Cooper, and J. B. de Haan (2009)
Arterioscler Thromb Vasc Biol
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Synergistic Growth Inhibition of Squamous Cell Carcinoma of the Head and Neck by Erlotinib and Epigallocatechin-3-Gallate: The Role of p53-Dependent Inhibition of Nuclear Factor-{kappa}B.
A. R. M. R. Amin, F. R. Khuri, Z. Chen, and D. M. Shin (2009)
Cancer Prevention Research
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KiSS1 Metastasis Suppressor Gene Product Induces Suppression of Tyrosine Kinase Receptor Signaling to Akt, Tumor Necrosis Factor Family Ligand Expression, and Apoptosis.
J.-M. Navenot, N. Fujii, and S. C. Peiper (2009)
Mol. Pharmacol.
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Pulsatile Stimulation Determines Timing and Specificity of NF-{kappa}B-Dependent Transcription.
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Science
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Pathogen Recognition and Inflammatory Signaling in Innate Immune Defenses.
Lipoic acid increases heat shock protein expression and inhibits stress kinase activation to improve insulin signaling in skeletal muscle from high-fat-fed rats.
A. A. Gupte, G. L. Bomhoff, J. K. Morris, B. K. Gorres, and P. C. Geiger (2009)
J Appl Physiol
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Heat Treatment Improves Glucose Tolerance and Prevents Skeletal Muscle Insulin Resistance in Rats Fed a High-Fat Diet.
A. A. Gupte, G. L. Bomhoff, R. H. Swerdlow, and P. C. Geiger (2009)
Diabetes
58, 567-578
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GGAP2/PIKE-A Directly Activates Both the Akt and Nuclear Factor-{kappa}B Pathways and Promotes Prostate Cancer Progression.
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Cancer Res.
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The Zinc Finger of NEMO Is a Functional Ubiquitin-binding Domain.
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284, 2902-2907
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Opposing functions of IKK{beta} during acute and chronic intestinal inflammation.
L. Eckmann, T. Nebelsiek, A. A. Fingerle, S. M. Dann, J. Mages, R. Lang, S. Robine, M. F. Kagnoff, R. M. Schmid, M. Karin, et al. (2008)
PNAS
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Interleukin (IL) 1{beta} Induction of IL-6 Is Mediated by a Novel Phosphatidylinositol 3-Kinase-dependent AKT/I{kappa}B Kinase {alpha} Pathway Targeting Activator Protein-1.
Essential Cytoplasmic Translocation of a Cytokine Receptor-Assembled Signaling Complex.
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Science
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Gonadotropin-regulated Testicular Helicase (DDX25), an Essential Regulator of Spermatogenesis, Prevents Testicular Germ Cell Apoptosis.
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Bacterial-Modulated Signaling Pathways in Gut Homeostasis.
Retinoic acid modulates chromatin to potentiate tumor necrosis factor alpha signaling on the DIF2 promoter.
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The NF-{kappa}B Canonical Pathway Is Involved in the Control of the Exonucleolytic Processing of Coding Ends during V(D)J Recombination.
M. M. Souto-Carneiro, R. Fritsch, N. Sepulveda, M. J. Lagareiro, N. Morgado, N. S. Longo, and P. E. Lipsky (2008)
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20-Hydroxyeicosatetraenoic Acid Stimulates Nuclear Factor-{kappa}B Activation and the Production of Inflammatory Cytokines in Human Endothelial Cells.
T. Ishizuka, J. Cheng, H. Singh, M. D. Vitto, V. L. Manthati, J. R. Falck, and M. Laniado-Schwartzman (2008)
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