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Crosstalk between NF-KB-Activating and Apoptosis-Inducting Proteins of the TNF-Receptor Complex

机译:TNF受体复合物的NF-KB激活蛋白和凋亡诱导蛋白之间的串扰

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摘要

The cytokine tumor necrosis factor (TNF ) elicits a wide range of biological responses, incluing inflammation, cell proliferation, differentiation , and apoptosis. Although the molecular mechanisms of TNF signaling have been largely elucidated, the principle that regulates the balance of life and death is still unknown. This review will focus on the crosstalk that exists between proteins of the TNF receptor(TNF-F) signalosome, and which are involved in the initiation of nuclear factor kappa B(NF-kB) activation or apoptoisis. At least four different mechanisms of regulation can be distinguished(i) NF-Kb-mediated induction of proteins of the TNF-R complex;(ii) NF-Kb-independent protection against apoptosis by the TNF-r-associating factor 2 (TRAF 2) -mediated recruitment of antiapoptotic proteins;(iii) dual activation of apoptosis and NF-kB by a signal molecule. and(iv) amplification of the death signal by proteolytic inactivation of signaling proteins that are involved in NF-kB activation or cell survival
机译:细胞因子肿瘤坏死因子(TNF)引起广泛的生物学反应,包括炎症,细胞增殖,分化和凋亡。尽管已经阐明了TNF信号传导的分子机制,但调节生死平衡的原理仍然未知。这项审查将侧重于TNF受体(TNF-F)信号小体的蛋白质之间存在的串扰,并且参与核因子κB(NF-kB)激活或凋亡的启动。至少可以区分四种不同的调节机制:(i)NF-Kb介导的TNF-R复合物蛋白的诱导;(ii)TNF-r相关因子2(TRAF)对NF-Kb的细胞凋亡的独立保护2)-介导的抗凋亡蛋白的募集;(iii)信号分子对凋亡和NF-κB的双重激活。 (iv)通过蛋白水解灭活涉及NF-kB激活或细胞存活的信号蛋白来扩增死亡信号

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