Hsu H, Shu H B, Pan M G, Goeddel D V
Tularik, Incorporated, South San Francisco, California 94080, USA.
Cell. 1996 Jan 26;84(2):299-308. doi: 10.1016/s0092-8674(00)80984-8.
Tumor necrosis factor (TNF) can induce apoptosis and activate NF-kappa B through signaling cascades emanating from TNF receptor 1 (TNFR1). TRADD is a TNFR1-associated signal transducer that is involved in activating both pathways. Here we show that TRADD directly interacts with TRAF2 and FADD, signal transducers that activate NF-kappa B and induce apoptosis, respectively. A TRAF2 mutant lacking its N-terminal RING finger domain is a dominant-negative inhibitor of TNF-mediated NF-kappa B activation, but does not affect TNF-induced apoptosis. Conversely, a FADD mutant lacking its N-terminal 79 amino acids is a dominant-negative inhibitor of TNF-induced apoptosis, but does not inhibit NF-kappa B activation. Thus, these two TNFR1-TRADD signaling cascades appear to bifurcate at TRADD.
肿瘤坏死因子(TNF)可通过源自肿瘤坏死因子受体1(TNFR1)的信号级联反应诱导细胞凋亡并激活核因子κB(NF-κB)。肿瘤坏死因子受体相关死亡结构域蛋白(TRADD)是一种与TNFR1相关的信号转导分子,参与激活这两条信号通路。在此我们表明,TRADD直接与肿瘤坏死因子受体相关因子2(TRAF2)和FADD相互作用,这两种信号转导分子分别激活NF-κB和诱导细胞凋亡。一种缺失其N端环状结构域的TRAF2突变体是TNF介导的NF-κB激活的显性负性抑制剂,但不影响TNF诱导的细胞凋亡。相反,一种缺失其N端79个氨基酸的FADD突变体是TNF诱导的细胞凋亡的显性负性抑制剂,但不抑制NF-κB激活。因此,这两条TNFR1-TRADD信号级联反应似乎在TRADD处发生分支。