A novel NINJ1-mediated regulatory step is essential for active membrane rupture and common to different cell death pathways.

Catarina Dias, Veit Hornung, Jesper Nylandsted
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引用次数: 1

Abstract

Plasma membrane rupture (PMR), the final event in lytic cell death that is in part responsible for the release of pro-inflammatory signals, was believed to be a passive event that followed osmotic swelling. Kayagaki et al. 1 have discovered that PMR is, in fact, mediated by ninjurin-1 (NINJ1), adding a novel regulatory step that is conserved across different types of lytic cell death, such as pyroptosis, necroptosis, and apoptosis. PMR is dependent on NINJ1 oligomerization, which is mediated by its highly conserved putative N-terminal α-helix. In vivo data suggest that the NINJ1-dependent secretome that is released upon PMR is likely to modulate antimicrobial host defense, suggesting this additional regulatory step also has physiological relevance.

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一个新的ninj1介导的调控步骤是活性膜破裂所必需的,并且在不同的细胞死亡途径中是共同的。
质膜破裂(PMR)是溶解性细胞死亡的最后一个事件,它在一定程度上负责促炎信号的释放,被认为是渗透性肿胀之后的被动事件。Kayagaki等人发现PMR实际上是由ninjurin-1 (NINJ1)介导的,增加了一个新的调控步骤,该步骤在不同类型的溶解性细胞死亡(如焦亡、坏死和凋亡)中是保守的。PMR依赖于NINJ1寡聚化,这是由其高度保守的n端α-螺旋介导的。体内数据表明,PMR释放的依赖于ninj1的分泌组可能调节抗微生物宿主防御,这表明这一额外的调节步骤也具有生理相关性。
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