NF-κ b活化蛋白与tnf受体复合物诱导凋亡蛋白间的串扰

Karen Heyninck, Rudi Beyaert
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引用次数: 79

摘要

肿瘤坏死因子(TNF)引发广泛的生物反应,包括炎症、细胞增殖、分化和凋亡。虽然TNF信号传导的分子机制已基本阐明,但其调节生与死平衡的原理仍是未知的。本文将对TNF受体(TNF- r)信号体蛋白之间的串扰进行综述,这些串扰参与了核因子κB (NF-κB)激活或凋亡的启动。至少有四种不同的调节机制可以区分:(i) NF-κ b介导的TNF-R复合物蛋白的诱导;(ii)通过tnf - r相关因子2 (TRAF2)介导的抗凋亡蛋白募集,NF-κ b不依赖于凋亡的保护作用;(iii)单分子双重激活细胞凋亡和NF-κB;(iv)通过蛋白水解使参与NF-κB活化或细胞存活的信号蛋白失活,放大死亡信号。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Crosstalk between NF-κB-Activating and Apoptosis-Inducing Proteins of the TNF-Receptor Complex

The cytokine tumor necrosis factor (TNF) elicits a wide range of biological responses, including 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-R) signalosome, and which are involved in the initiation of nuclear factor kappa B (NF-κB) activation or apoptosis. At least four different mechanisms of regulation can be distinguished: (i) NF-κB-mediated induction of proteins of the TNF-R complex; (ii) NF-κB-independent protection against apoptosis by the TNF-R-associating factor 2 (TRAF2)-mediated recruitment of antiapoptotic proteins; (iii) dual activation of apoptosis and NF-κB by a single molecule; and (iv) amplification of the death signal by proteolytic inactivation of signaling proteins that are involved in NF-κB activation or cell survival.

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