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本文引用的文献

1
MLKL, the Protein that Mediates Necroptosis, Also Regulates Endosomal Trafficking and Extracellular Vesicle Generation.MLKL,介导细胞坏死的蛋白质,也调节内体运输和细胞外囊泡的产生。
Immunity. 2017 Jul 18;47(1):51-65.e7. doi: 10.1016/j.immuni.2017.06.001. Epub 2017 Jun 27.
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Initiation and execution mechanisms of necroptosis: an overview.坏死性凋亡的起始与执行机制:综述
Cell Death Differ. 2017 Jul;24(7):1184-1195. doi: 10.1038/cdd.2017.65. Epub 2017 May 12.
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Ferroptosis: bug or feature?铁死亡:缺陷还是特性?
Immunol Rev. 2017 May;277(1):150-157. doi: 10.1111/imr.12533.
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The in vivo evidence for regulated necrosis.细胞程序性坏死的体内证据。
Immunol Rev. 2017 May;277(1):128-149. doi: 10.1111/imr.12551.
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ESCRT-III Acts Downstream of MLKL to Regulate Necroptotic Cell Death and Its Consequences.ESCRT-III在混合谱系激酶结构域样蛋白(MLKL)下游发挥作用,以调节坏死性凋亡细胞死亡及其后果。
Cell. 2017 Apr 6;169(2):286-300.e16. doi: 10.1016/j.cell.2017.03.020.
6
On the Mechanism of Cytoprotection by Ferrostatin-1 and Liproxstatin-1 and the Role of Lipid Peroxidation in Ferroptotic Cell Death.铁抑素-1和脂氧抑素-1的细胞保护机制以及脂质过氧化在铁死亡细胞死亡中的作用
ACS Cent Sci. 2017 Mar 22;3(3):232-243. doi: 10.1021/acscentsci.7b00028. Epub 2017 Mar 7.
7
Ferroptosis Inhibition: Mechanisms and Opportunities.铁死亡抑制:机制与机遇。
Trends Pharmacol Sci. 2017 May;38(5):489-498. doi: 10.1016/j.tips.2017.02.005. Epub 2017 Mar 28.
8
Characterization of ferroptosis in murine models of hemochromatosis.血色素沉着症小鼠模型中铁死亡的特征描述。
Hepatology. 2017 Aug;66(2):449-465. doi: 10.1002/hep.29117. Epub 2017 May 16.
9
Heat stress induces ferroptosis-like cell death in plants.热胁迫诱导植物发生铁死亡样细胞死亡。
J Cell Biol. 2017 Feb;216(2):463-476. doi: 10.1083/jcb.201605110. Epub 2017 Jan 18.
10
Insane in the membrane: a structural perspective of MLKL function in necroptosis.膜内之“疯狂”:坏死性凋亡中混合谱系激酶结构域样蛋白功能的结构视角
Immunol Cell Biol. 2017 Feb;95(2):152-159. doi: 10.1038/icb.2016.125. Epub 2017 Jan 17.

铁死亡如何融入调控性细胞死亡家族?

How do we fit ferroptosis in the family of regulated cell death?

机构信息

Pharmacology and Therapeutics, Biomedical Sciences, Dangan, NUI Galway, Galway, Ireland.

VIB Inflammation Research Center, Ghent, Belgium.

出版信息

Cell Death Differ. 2017 Dec;24(12):1991-1998. doi: 10.1038/cdd.2017.149. Epub 2017 Oct 6.

DOI:10.1038/cdd.2017.149
PMID:28984871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5686356/
Abstract

In the last few years many new cell death modalities have been described. To classify different types of cell death, the term 'regulated cell death' was introduced to discriminate it from 'accidental cell death'. Regulated cell death involves the activation of genetically encoded molecular machinery that couples the presence of some signal to cell death. These forms of cell death, like apoptosis, necroptosis and pyroptosis have important physiological roles in development, tissue repair, and immunity. Accidental cell death occurs in response to physical or chemical insults and occurs independently of molecular signalling pathways. Ferroptosis, an emerging and recently (re)discovered type of regulated cell death occurs through Fe(II)-dependent lipid peroxidation when the reduction capacity of a cell is insufficient. Ferroptosis is coined after the requirement for free ferrous iron. Here, we will consider the extent to which ferroptosis is similar to other regulated cell deaths and explore emerging ideas about the physiological role of ferroptosis.

摘要

在过去的几年中,已经描述了许多新的细胞死亡方式。为了对不同类型的细胞死亡进行分类,引入了“程序性细胞死亡”一词,将其与“意外细胞死亡”区分开来。程序性细胞死亡涉及到激活基因编码的分子机制,将某些信号与细胞死亡联系起来。这些形式的细胞死亡,如细胞凋亡、坏死性凋亡和细胞焦亡,在发育、组织修复和免疫中具有重要的生理作用。意外细胞死亡是对物理或化学损伤的反应,独立于分子信号通路发生。铁死亡是一种新出现的、最近(重新)发现的程序性细胞死亡类型,当细胞的还原能力不足时,通过铁依赖性脂质过氧化发生。铁死亡这个词是由游离亚铁的需求衍生而来的。在这里,我们将考虑铁死亡与其他程序性细胞死亡的相似程度,并探讨铁死亡的生理作用的新观点。