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Article: From antigen to activation: Specific signal transduction pathways linking antigen receptors to NF-κB

TitleFrom antigen to activation: Specific signal transduction pathways linking antigen receptors to NF-κB
Authors
KeywordsLymphocyte
Antigen receptor
NF-κB
Signal transduction
BCL10
Issue Date2003
Citation
Seminars in Immunology, 2003, v. 15, n. 3, p. 177-183 How to Cite?
AbstractA precise balance between cellular apoptosis and cellular survival is essential for the proper functioning of the immune system. Whereas apoptosis eliminates self-reactive or supernumerary lymphocytes, survival signaling that counteracts apoptotic programs is needed to allow B and T lymphocytes that recognize pathogens to become activated and expand in response to infection. A major regulator of lymphocyte survival and activation is the transcription factor NF-κB. Controlled activation of NF-κB is essential for normal innate and adaptive immune responses, and dysregulated NF-κB signaling in lymphocytes contributes to diseases ranging from chronic inflammation and autoimmunity to lymphoma. The core NF-κB activating machinery composed of the NF-κB, IκB and IKK proteins is relatively well-characterized, but it is less clear how distinct upstream stimuli activate NF-κB in a tissue-, time- and signal-specific manner. In this review, we discuss recent insights into the specific signal transduction pathways leading to NF-κB activation that are triggered by engagement of the antigen receptors of T and B cells. We focus mainly on T cell receptor (TCR)-mediated NF-κB activation and draw parallels to B cell receptor (BCR)-mediated NF-κB activation where appropriate. © 2003 Published by Elsevier Science Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/291674
ISSN
2021 Impact Factor: 10.671
2020 SCImago Journal Rankings: 3.765
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorRuland, Jürgen-
dc.contributor.authorMak, Tak W.-
dc.date.accessioned2020-11-17T14:54:52Z-
dc.date.available2020-11-17T14:54:52Z-
dc.date.issued2003-
dc.identifier.citationSeminars in Immunology, 2003, v. 15, n. 3, p. 177-183-
dc.identifier.issn1044-5323-
dc.identifier.urihttp://hdl.handle.net/10722/291674-
dc.description.abstractA precise balance between cellular apoptosis and cellular survival is essential for the proper functioning of the immune system. Whereas apoptosis eliminates self-reactive or supernumerary lymphocytes, survival signaling that counteracts apoptotic programs is needed to allow B and T lymphocytes that recognize pathogens to become activated and expand in response to infection. A major regulator of lymphocyte survival and activation is the transcription factor NF-κB. Controlled activation of NF-κB is essential for normal innate and adaptive immune responses, and dysregulated NF-κB signaling in lymphocytes contributes to diseases ranging from chronic inflammation and autoimmunity to lymphoma. The core NF-κB activating machinery composed of the NF-κB, IκB and IKK proteins is relatively well-characterized, but it is less clear how distinct upstream stimuli activate NF-κB in a tissue-, time- and signal-specific manner. In this review, we discuss recent insights into the specific signal transduction pathways leading to NF-κB activation that are triggered by engagement of the antigen receptors of T and B cells. We focus mainly on T cell receptor (TCR)-mediated NF-κB activation and draw parallels to B cell receptor (BCR)-mediated NF-κB activation where appropriate. © 2003 Published by Elsevier Science Ltd.-
dc.languageeng-
dc.relation.ispartofSeminars in Immunology-
dc.subjectLymphocyte-
dc.subjectAntigen receptor-
dc.subjectNF-κB-
dc.subjectSignal transduction-
dc.subjectBCL10-
dc.titleFrom antigen to activation: Specific signal transduction pathways linking antigen receptors to NF-κB-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/S1044-5323(03)00034-4-
dc.identifier.pmid14563116-
dc.identifier.scopuseid_2-s2.0-0742287249-
dc.identifier.volume15-
dc.identifier.issue3-
dc.identifier.spage177-
dc.identifier.epage183-
dc.identifier.isiWOS:000184400600007-
dc.identifier.issnl1044-5323-

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