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DAI可感知甲型流感病毒基因组RNA并激活依赖RIPK3的细胞死亡。

DAI Senses Influenza A Virus Genomic RNA and Activates RIPK3-Dependent Cell Death.

作者信息

Thapa Roshan J, Ingram Justin P, Ragan Katherine B, Nogusa Shoko, Boyd David F, Benitez Asiel A, Sridharan Haripriya, Kosoff Rachelle, Shubina Maria, Landsteiner Vanessa J, Andrake Mark, Vogel Peter, Sigal Luis J, tenOever Benjamin R, Thomas Paul G, Upton Jason W, Balachandran Siddharth

机构信息

Blood Cell Development and Function Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.

Department of Molecular Biosciences, LaMontagne Center for Infectious Disease, University of Texas, Austin, TX 78712, USA.

出版信息

Cell Host Microbe. 2016 Nov 9;20(5):674-681. doi: 10.1016/j.chom.2016.09.014. Epub 2016 Oct 13.

Abstract

Influenza A virus (IAV) is an RNA virus that is cytotoxic to most cell types in which it replicates. IAV activates the host kinase RIPK3, which induces cell death via parallel pathways of necroptosis, driven by the pseudokinase MLKL, and apoptosis, dependent on the adaptor proteins RIPK1 and FADD. How IAV activates RIPK3 remains unknown. We report that DAI (ZBP1/DLM-1), previously implicated as a cytoplasmic DNA sensor, is essential for RIPK3 activation by IAV. Upon infection, DAI recognizes IAV genomic RNA, associates with RIPK3, and is required for recruitment of MLKL and RIPK1 to RIPK3. Cells lacking DAI or containing DAI mutants deficient in nucleic acid binding are resistant to IAV-triggered necroptosis and apoptosis. DAI-deficient mice fail to control IAV replication and succumb to lethal respiratory infection. These results identify DAI as a link between IAV replication and RIPK3 activation and implicate DAI as a sensor of RNA viruses.

摘要

甲型流感病毒(IAV)是一种RNA病毒,对其进行复制的大多数细胞类型具有细胞毒性。IAV激活宿主激酶RIPK3,RIPK3通过由假激酶MLKL驱动的坏死性凋亡平行途径和依赖衔接蛋白RIPK1和FADD的凋亡诱导细胞死亡。IAV如何激活RIPK3仍然未知。我们报告称,DAI(ZBP1/DLM-1),先前被认为是一种细胞质DNA传感器,对于IAV激活RIPK3至关重要。感染后,DAI识别IAV基因组RNA,与RIPK3结合,并且是将MLKL和RIPK1募集到RIPK3所必需的。缺乏DAI或含有核酸结合缺陷的DAI突变体的细胞对IAV触发的坏死性凋亡和凋亡具有抗性。缺乏DAI的小鼠无法控制IAV复制,并死于致命的呼吸道感染。这些结果确定DAI是IAV复制与RIPK3激活之间的联系,并表明DAI是RNA病毒的传感器。

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1
ZBP1/DAI is an innate sensor of influenza virus triggering the NLRP3 inflammasome and programmed cell death pathways.
Sci Immunol. 2016 Aug 5;1(2). doi: 10.1126/sciimmunol.aag2045. Epub 2016 Aug 12.
2
RIPK3 Activates Parallel Pathways of MLKL-Driven Necroptosis and FADD-Mediated Apoptosis to Protect against Influenza A Virus.
Cell Host Microbe. 2016 Jul 13;20(1):13-24. doi: 10.1016/j.chom.2016.05.011. Epub 2016 Jun 16.
3
Influenza A Virus Panhandle Structure Is Directly Involved in RIG-I Activation and Interferon Induction.
J Virol. 2015 Jun;89(11):6067-79. doi: 10.1128/JVI.00232-15. Epub 2015 Mar 25.
4
Single-molecule FRET reveals a corkscrew RNA structure for the polymerase-bound influenza virus promoter.
Proc Natl Acad Sci U S A. 2014 Aug 12;111(32):E3335-42. doi: 10.1073/pnas.1406056111. Epub 2014 Jul 28.
5
RIPK1 both positively and negatively regulates RIPK3 oligomerization and necroptosis.
Cell Death Differ. 2014 Oct;21(10):1511-21. doi: 10.1038/cdd.2014.76. Epub 2014 Jun 6.
6
RIPK1- and RIPK3-induced cell death mode is determined by target availability.
Cell Death Differ. 2014 Oct;21(10):1600-12. doi: 10.1038/cdd.2014.70. Epub 2014 Jun 6.
7
Characterization of innate responses to influenza virus infection in a novel lung type I epithelial cell model.
J Gen Virol. 2014 Feb;95(Pt 2):350-362. doi: 10.1099/vir.0.058438-0. Epub 2013 Nov 16.
9
Zalpha-domains: at the intersection between RNA editing and innate immunity.
Semin Cell Dev Biol. 2012 May;23(3):275-80. doi: 10.1016/j.semcdb.2011.11.001. Epub 2011 Nov 7.
10
Adenosine deaminases acting on RNA (ADARs) are both antiviral and proviral.
Virology. 2011 Mar 15;411(2):180-93. doi: 10.1016/j.virol.2010.12.004. Epub 2011 Jan 5.

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