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pubmed-article:9151703pubmed:issue10lld:pubmed
pubmed-article:9151703pubmed:dateCreated1997-6-24lld:pubmed
pubmed-article:9151703pubmed:abstractTextTumor necrosis factor receptor (TNFR)-associated factor 2 (TRAF2) and TRAF1 were found as components of the TNFR2 signaling complex, which exerts multiple biological effects on cells such as cell proliferation, cytokine production, and cell death. In the TNFR2-mediated signaling pathways, TRAF2 works as a mediator for activation signals such as NF-kappaB, but the role of TRAF1 has not been previously determined. Here we show in transgenic mice that TRAF1 overexpression inhibits antigen-induced apoptosis of CD8(+) T lymphocytes. Our results demonstrate a biological role for TRAF1 as a regulator of apoptotic signals and also support the hypothesis that the combination of TRAF proteins in a given cell type determines distinct biological effects triggered by members of the TNF receptor superfamily.lld:pubmed
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pubmed-article:9151703pubmed:statusMEDLINElld:pubmed
pubmed-article:9151703pubmed:monthMaylld:pubmed
pubmed-article:9151703pubmed:issn0022-1007lld:pubmed
pubmed-article:9151703pubmed:authorpubmed-author:LeeS YSYlld:pubmed
pubmed-article:9151703pubmed:authorpubmed-author:WongBBlld:pubmed
pubmed-article:9151703pubmed:authorpubmed-author:ChoiYYlld:pubmed
pubmed-article:9151703pubmed:authorpubmed-author:SpeiserD EDElld:pubmed
pubmed-article:9151703pubmed:authorpubmed-author:SantanaAAlld:pubmed
pubmed-article:9151703pubmed:authorpubmed-author:OhashiP SPSlld:pubmed
pubmed-article:9151703pubmed:authorpubmed-author:KongY YYYlld:pubmed
pubmed-article:9151703pubmed:authorpubmed-author:ArronJJlld:pubmed
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pubmed-article:9151703pubmed:day19lld:pubmed
pubmed-article:9151703pubmed:volume185lld:pubmed
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pubmed-article:9151703pubmed:pagination1777-83lld:pubmed
pubmed-article:9151703pubmed:dateRevised2009-11-18lld:pubmed
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