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NF-kappaB and inflammation in genetic disease
Authors:Sebban Hélène  Courtois Gilles
Affiliation:INSERM U697, Pavillon Bazin, H?pital Saint-Louis, 1, Avenue Claude Vellefaux, 75010 Paris, France.
Abstract:
By responding to pro-inflammatory cytokines, such as IL-1beta and TNF-alpha, and controlling itself the expression of numerous mediators of inflammation, NF-kappaB plays a pivotal role in controlling the proper sequence of events characterizing the inflammation process. Although excessive NF-kappaB activation is often associated with inflammatory signs in many different tissues, impaired NF-kappaB activation can also generate inflammation. This is the case in humans suffering from the genetic disease incontinentia pigmenti that exhibit severe skin inflammation. Identifying the molecular basis of this pathology, mutations affecting the gene coding for NEMO, has allowed production of mouse models for investigating the disease. Their characterization supports the view that a very tight positive and negative regulation of the NF-kappaB signaling pathway is required in vivo to ensure not only a fine-tuned response to injury or infection but also to maintain tissue homeostasis.
Keywords:CFTR, cystic fibrosis transmembrane conductance regulator   EDA-ID, anhidrotic ectodermal dysplasia with immunodeficiency   IκB, IkappaB   IKK, IκB kinase   IL-1, interleukin-1   IL-1-R, interleukin-1-receptor   IL-1RacP, IL-1 receptor accessory protein   iNOS, inducible nitric oxide synthase   IP, incontinentia pigmenti   IRAK, IL-1 receptor associated kinase   LPS, lipopolysaccharide   NEMO, NF-κB essential modulator   NF-κB, nuclear factor-kappa B   NOD, nucleotide-binding oligomerization domain   RIP, receptor interacting protein   TAB, TAK1-binding protein   TAK, TGF-β activated kinase   TIR, Toll/IL-1 receptor domain   TIRAP, TIR domain-containing adaptor protein   TLR, Toll-like receptor   TNF, tumor necrosis factor   TNF-R, TNF-receptor   TRADD, TNF-receptor-associated death domain protein   TRAF, TNF receptor-associated factor   TRAM, TRIF-related adapter molecule   TRIF, TIR-domain-containing adapter-inducing IFN-β
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