坏死:MLKL聚合。

Journal of nature and science Pub Date : 2018-07-01
Andrea Johnston, Zhigao Wang
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引用次数: 0

摘要

坏死是一种调节性坏死的亚型,当半胱天冬酶被抑制或未能激活时就会发生。细胞死亡受体的刺激导致信号级联,触发胱天蛋白酶非依赖性的免疫原性细胞死亡。核心途径依赖于受体相互作用蛋白激酶(RIPK)1和3,它们通过受体同源相互作用基序(RHIM)结构域相互作用,并形成称为坏死小体的淀粉样结构。RIPK3募集并磷酸化坏死途径中的末端介质混合谱系激酶结构域样假激酶(MLKL)。MLKL聚合形成第二个淀粉样结构,导致细胞膜破裂,导致细胞死亡。尽管核心坏死途径已经阐明,但MLKL膜移位和膜破坏的细节仍然是一个开放的研究领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Necroptosis: MLKL Polymerization.

Necroptosis is a subtype of regulated necrosis that occurs when caspases are inhibited or fail to activate. Stimulus of cell death receptors results in a signaling cascade that triggers caspase independent, immunogenic cell death. The core pathway relies on receptor interacting protein kinase (RIPK) 1 and 3, which interact through their receptor homotypic interacting motif (RHIM) domains, and form amyloid-like structures termed the necrosome. RIPK3 recruits and phosphorylates mixed lineage kinase domain-like pseudokinase (MLKL), the terminal mediator in the necroptotic pathway. MLKL polymerizes to form a second amyloid-like structure that causes cell membrane disruption resulting in cell death. Although the core necroptosis pathway has been elucidated, the details of MLKL membrane translocation and membrane disruption remain an open area of research.

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