肿瘤坏死因子α
交通2
细胞生物学
信号转导
NF-κB
转录因子
调解人
IκB激酶
细胞因子
NFKB1型
刺激
生物
促炎细胞因子
炎症
化学
免疫学
神经科学
肿瘤坏死因子受体
生物化学
基因
出处
期刊:Cytokine
[Elsevier]
日期:2008-01-01
卷期号:41 (1): 1-8
被引量:159
标识
DOI:10.1016/j.cyto.2007.09.016
摘要
Tumor Necrosis Factor alpha (TNFalpha) is a pro-inflammatory cytokine that plays important roles in different biological processes, including the induction of other cytokines. One of the most important downstream signaling targets activated by TNFalpha is the NF-kappaB transcription factor, which has been identified to be involved in inflammatory, anti-apoptotic, and immune responses. Stimulation of cells with TNFalpha triggers activation of NF-kappaB through various signaling molecules, including TRAF2, RIP, MAP3K, and the IKK complex. Recently, numerous studies have been performed to explore the detailed mechanism by which NF-kappaB is activated upon TNFalpha stimulation. Current understanding of this pathway has been focused on the identification of signaling components, the role of post-translational modification and the sub-cellular translocation of those components. Additionally, more negative regulators in the TNF-IKK pathway are emerging.
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