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RIPK3调节的坏死的执行

Execution of RIPK3-regulated necrosis.

作者信息

Cai Zhenyu, Liu Zheng-Gang

机构信息

Center for Cancer Research; National Cancer Institute; National Institutes of Health , Bethesda, MD USA.

出版信息

Mol Cell Oncol. 2014 Oct 29;1(2):e960759. doi: 10.4161/23723548.2014.960759. eCollection 2014 Apr-Jun.

Abstract

Necroptosis is a form of regulated necrotic cell death that is mediated by receptor-interacting protein 1 (RIP1) and RIP3 kinases. Diverse receptors, including death receptors, Toll-like receptors, interferon receptors, and DAI DNA receptors are able to trigger necroptosis. The newly identified MLKL protein functions downstream of RIP1/RIP3 and is essential for the execution of necroptosis. Studies also indicate involvement of reactive oxygen species and calcium and sodium ions. Identification of the key mediators of necroptosis is critical for understanding the molecular mechanisms of the necroptotic process.

摘要

坏死性凋亡是一种由受体相互作用蛋白1(RIP1)和RIP3激酶介导的程序性坏死性细胞死亡形式。包括死亡受体、Toll样受体、干扰素受体和DAI DNA受体在内的多种受体能够触发坏死性凋亡。新鉴定出的混合谱系激酶结构域样蛋白(MLKL)在RIP1/RIP3的下游发挥作用,是坏死性凋亡执行过程所必需的。研究还表明活性氧以及钙和钠离子也参与其中。鉴定坏死性凋亡的关键介质对于理解坏死性凋亡过程的分子机制至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dac/4905176/acd67a0d7971/kmco-01-02-960759-g001.jpg

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