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PMID: 16439988 Published · ppublish English Journal Article Review

Deciphering the pathway from the TCR to NF-kappaB.

Cell death and differentiation ·Vol. 13 ·No. 5 ·2006-05-00 ·Pages 826-33

Weil R, Israël A

Abstract

A major regulator of lymphocyte survival and activation is the transcription factor nuclear factor-kappaB (NF-kappaB). Controlled activation of NF-kappaB is essential for the immune and inflammatory response as well as for cell proliferation and protection against apoptosis. The NEMO/IkappaB kinase (IKK) complex is the central integrator of most stimuli leading to NF-kappaB activation, but a detailed knowledge of the upstream events is available only for a limited number of stimuli. In particular, although most players have probably been identified, relatively little is known about the detailed molecular mechanisms involved in the cascade leading to NF-kappaB activation following engagement of the T-cell receptor by a foreign antigen. In this review, we discuss recent insights into this specific signal transduction cascade, and the way it is controlled both spatially and temporally.

MeSH Terms
Adaptor Proteins, Signal Transducing/metabolism Apoptosis Regulatory Proteins/metabolism Gene Expression Regulation Humans I-kappa B Kinase/metabolism Lymphoma, B-Cell, Marginal Zone/metabolism Models, Biological NF-kappa B/metabolism Protein Kinase C/metabolism Receptors, Antigen, T-Cell/metabolism Signal Transduction
Chemicals
Adaptor Proteins, Signal Transducing Apoptosis Regulatory Proteins NF-kappa B Receptors, Antigen, T-Cell I-kappa B Kinase Protein Kinase C
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Weil R
Unité de Signalisation Moléculaire et Activation Cellulaire, URA 2582 Centre National de la Recherche Scientifique, Institut Pasteur, 25 Rue du Dr. Roux, 75724 Paris Cedex 15, France.
Israël A
Article Info
Journal
Cell death and differentiation
Abbr.
Cell Death Differ
ISSN
1350-9047
Published
2006-05-00
Pages
826-33
Language
English
Region
England
NLM ID
9437445
Subset
IM
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