The distinct roles of TRAF2 and RIP in IKK activation by TNF-R1: TRAF2 recruits IKK to TNF-R1 while RIP mediates IKK activation

被引:366
作者
Devin, A
Cook, A
Lin, Y
Rodriguez, Y
Kelliher, M
Liu, ZG [1 ]
机构
[1] NCI, Dept Cell & Canc Biol, Med Branch, Div Clin Sci,NIH, Bethesda, MD 20892 USA
[2] Univ Massachusetts, Med Ctr, Worcester, MA 01605 USA
关键词
D O I
10.1016/S1074-7613(00)80194-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The death domain kinase RIP and the TNF receptor-associated factor 2 (TRAF2) are essential effecters in TNF signaling. To understand the mechanism by which RIP and TRAF2 regulate TNF-induced activation of the transcription factor NF-KB, we investigated their respective roles in TNF-R1-mediated IKK activation using both RIP-/- and TRAF2(-/-) fibroblasts. We found that TNF-R1-mediated IKK activation requires both RIP and TRAF2 proteins. Although TRAF2 or RIP can be independently recruited to the TNF-R1 complex, neither one of them alone is capable of transducing the TNF signal that leads to IKK activation. Moreover, we demonstrated that IKK is recruited to the TNF-R1 complex through TRAF2 upon TNF treatment and that IKK activation requires the presence of RIP in the same complex.
引用
收藏
页码:419 / 429
页数:11
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