贸易
时尚
交通2
生物
细胞生物学
下调和上调
肿瘤坏死因子受体1
半胱氨酸蛋白酶8
受体
半胱氨酸蛋白酶
癌症研究
坏死性下垂
胞浆
细胞凋亡
信号转导
死亡域
肿瘤坏死因子α
程序性细胞死亡
肿瘤坏死因子受体
免疫学
生物化学
酶
基因
作者
M. Saeed Sheikh,Ying Huang
出处
期刊:Cell Cycle
[Taylor & Francis]
日期:2003-11-28
卷期号:2 (6): 549-551
被引量:111
摘要
The extrinsic pathway of apoptosis originates at the membrane and engages membrane death receptors. Tumor necrosis factor receptor 1 (TNF-R1) is a death receptor that transduces both the death and survival signals but the molecular mechanisms via which TNF-R1 mediates these signals remain poorly understood. Recently, it has been reported that the TNF-R1 transduces these signals via two signaling complexes. The first complex (complex I) is formed at the membrane by TNF-R1, TRADD, RIP, TRAF2 and c-IAP1, while the second complex (complex II), formed in the cytosol, predominantly contains FADD and pro-caspases 8/10 but lacks TNF-R1. Complex I is responsible for activating NF-kappaB and thus, the transduction of survival signals. Complex II, on the other hand, is reported to transduce the apoptotic signals and it does so only if NF-kappaB is unable to promote upregulation of the anti-apoptotic FLIPL. These findings highlighting the complexities of TNF-R1-mediated signaling events are likely to further the progress in the constantly evolving area of death receptor-dependent signaling pathways.
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