坏死性下垂
生物
程序性细胞死亡
干扰素
细胞生物学
信号转导
串扰
裂谷1
先天免疫系统
细胞凋亡
免疫学
免疫系统
遗传学
光学
物理
作者
Xinyu Chen,Yinghong Dai,Xin-xing Wan,Xi‐min Hu,Wenjuan Zhao,Xiao-Xia Ban,Hao Wan,Kun Huang,Qí Zhāng,Kun Xiong
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2022-12-21
卷期号:28 (1): 52-52
被引量:20
标识
DOI:10.3390/molecules28010052
摘要
Cell death is a fundamental pathophysiological process in human disease. The discovery of necroptosis, a form of regulated necrosis that is induced by the activation of death receptors and formation of necrosome, represents a major breakthrough in the field of cell death in the past decade. Z-DNA-binding protein (ZBP1) is an interferon (IFN)-inducing protein, initially reported as a double-stranded DNA (dsDNA) sensor, which induces an innate inflammatory response. Recently, ZBP1 was identified as an important sensor of necroptosis during virus infection. It connects viral nucleic acid and receptor-interacting protein kinase 3 (RIPK3) via two domains and induces the formation of a necrosome. Recent studies have also reported that ZBP1 induces necroptosis in non-viral infections and mediates necrotic signal transduction by a unique mechanism. This review highlights the discovery of ZBP1 and its novel findings in necroptosis and provides an insight into its critical role in the crosstalk between different types of cell death, which may represent a new therapeutic option.
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