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慢性预言死亡:TNF 信号中的双重顺序细胞死亡检查点。

Chronicles of a death foretold: dual sequential cell death checkpoints in TNF signaling.

机构信息

Immunology Institute, Mount Sinai School of Medicine, New York, NY, USA.

出版信息

Cell Cycle. 2010 Mar 15;9(6):1065-71. doi: 10.4161/cc.9.6.10982.

Abstract

The kinase RIP1 wears a coat of many colors during TNF receptor signaling and can regulate both activation of pro-survival NFkB and programmed cell death pathways. In this review, we outline how coating RIP1 with K63-linked ubiquitin chains forms a protective layer that prevents RIP1 from binding apoptotic regulators and serves as an early guard against cell death. Further on, binding of NFkB signaling components to the ubiquitin coat of RIP1 activates long-term pro-survival signaling and forms a more impenetrable suit of armor against cell death. If RIP1 is not decorated with ubiquitin chains it becomes an unstoppable harbinger of bad news: programmed cell death.

摘要

激酶 RIP1 在 TNF 受体信号转导过程中扮演着多重角色,能够调节促生存 NFkB 和程序性细胞死亡途径的激活。在这篇综述中,我们概述了 RIP1 被 K63 连接的泛素链包裹如何形成一个保护层,防止 RIP1 与凋亡调节因子结合,并作为细胞死亡的早期防护。此外,NFkB 信号成分与 RIP1 泛素涂层的结合激活了长期的促生存信号,并形成了更坚固的对抗细胞死亡的盔甲。如果 RIP1 没有被泛素链修饰,它就会成为一个不可阻挡的坏消息的先兆:程序性细胞死亡。

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