Interferons command Trim22 to fight against viruses.
作者信息
Lian Qiaoshi, Sun Bing
机构信息
State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai 200031, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
出版信息
Cell Mol Immunol. 2017 Sep;14(9):794-796. doi: 10.1038/cmi.2017.76. Epub 2017 Aug 7.
Abstract
摘要
相似文献
1
Interferons command Trim22 to fight against viruses.
Cell Mol Immunol. 2017 Sep;14(9):794-796. doi: 10.1038/cmi.2017.76. Epub 2017 Aug 7.
2
Mutations Conferring Increased Sensitivity to Tripartite Motif 22 Restriction Accumulated Progressively in the Nucleoprotein of Seasonal Influenza A (H1N1) Viruses between 1918 and 2009.
mSphere. 2018 Apr 4;3(2). doi: 10.1128/mSphere.00110-18. Print 2018 Apr 25.
3
TRIM22. A Multitasking Antiviral Factor.
Cells. 2021 Jul 23;10(8):1864. doi: 10.3390/cells10081864.
4
TRIM22 inhibits endometrial cancer progression through the NOD2/NF‑κB signaling pathway and confers a favorable prognosis.
Int J Oncol. 2020 May;56(5):1225-1239. doi: 10.3892/ijo.2020.5004. Epub 2020 Mar 4.
5
TRIM22 regulates macrophage autophagy and enhances Mycobacterium tuberculosis clearance by targeting the nuclear factor-multiplicity κB/beclin 1 pathway.
J Cell Biochem. 2018 Nov;119(11):8971-8980. doi: 10.1002/jcb.27153. Epub 2018 Jul 16.
6
The interferon-stimulated gene TRIM22: A double-edged sword in HIV-1 infection.
Cytokine Growth Factor Rev. 2018 Apr;40:40-47. doi: 10.1016/j.cytogfr.2018.02.001. Epub 2018 Feb 10.
7
TRIM22-Mediated Apoptosis is Associated with Bak Oligomerization in Monocytes.
Sci Rep. 2017 Jan 12;7:39961. doi: 10.1038/srep39961.
8
Tripartite motif-containing 22 inhibits the activity of hepatitis B virus core promoter, which is dependent on nuclear-located RING domain.
Hepatology. 2009 Aug;50(2):424-33. doi: 10.1002/hep.23011.
9
Variants in TRIM22 That Affect NOD2 Signaling Are Associated With Very-Early-Onset Inflammatory Bowel Disease.
Gastroenterology. 2016 May;150(5):1196-1207. doi: 10.1053/j.gastro.2016.01.031. Epub 2016 Feb 4.
10
Knockdown of Tripartite motif-containing 22 (TRIM22)relieved the apoptosis of lens epithelial cells by suppressing the expression of TNF receptor-associated factor 6 (TRAF6).
Bioengineered. 2021 Dec;12(1):7213-7222. doi: 10.1080/21655979.2021.1980645.
引用本文的文献
1
SARS-CoV-2 variants induce increased inflammatory gene expression but reduced interferon responses and heme synthesis as compared with wild type strains.
Sci Rep. 2024 Oct 28;14(1):25734. doi: 10.1038/s41598-024-76401-1.
2
Severe Asthma and Biological Therapies: Now and the Future.
J Clin Med. 2023 Sep 8;12(18):5846. doi: 10.3390/jcm12185846.
3
Impact of TRIM5α and TRIM22 Genes Expression on the Clinical Course of Coronavirus Disease 2019.
Arch Med Res. 2023 Feb;54(2):105-112. doi: 10.1016/j.arcmed.2022.12.010. Epub 2022 Dec 28.
4
D2I and F9Y Mutations in the NS1 Protein of Influenza A Virus Affect Viral Replication via Regulating Host Innate Immune Responses.
Viruses. 2022 Jun 1;14(6):1206. doi: 10.3390/v14061206.
5
Large-scale genomic study reveals robust activation of the immune system following advanced Inner Engineering meditation retreat.
Proc Natl Acad Sci U S A. 2021 Dec 21;118(51). doi: 10.1073/pnas.2110455118.
6
TRIM22. A Multitasking Antiviral Factor.
Cells. 2021 Jul 23;10(8):1864. doi: 10.3390/cells10081864.
7
Dual R108K and G189D Mutations in the NS1 Protein of A/H1N1 Influenza Virus Counteract Host Innate Immune Responses.
Viruses. 2021 May 13;13(5):905. doi: 10.3390/v13050905.
8
Network Analysis and Transcriptome Profiling Identify Autophagic and Mitochondrial Dysfunctions in SARS-CoV-2 Infection.
Front Genet. 2021 Mar 16;12:599261. doi: 10.3389/fgene.2021.599261. eCollection 2021.
9
Induction and Evasion of Type-I Interferon Responses during Influenza A Virus Infection.
Cold Spring Harb Perspect Med. 2021 Oct 1;11(10):a038414. doi: 10.1101/cshperspect.a038414.
10
Network Analysis and Transcriptome Profiling Identify Autophagic and Mitochondrial Dysfunctions in SARS-CoV-2 Infection.
bioRxiv. 2020 Jul 20:2020.05.13.092536. doi: 10.1101/2020.05.13.092536.
本文引用的文献
1
Laboratory of genetics and physiology 2 (LGP2) plays an essential role in hepatitis C virus infection-induced interferon responses.
Hepatology. 2017 May;65(5):1478-1491. doi: 10.1002/hep.29050. Epub 2017 Mar 30.
2
Relationship of TRIM5 and TRIM22 polymorphisms with liver disease and HCV clearance after antiviral therapy in HIV/HCV coinfected patients.
J Transl Med. 2016 Sep 2;14(1):257. doi: 10.1186/s12967-016-1005-7.
3
Interferon alpha (IFNα)-induced TRIM22 interrupts HCV replication by ubiquitinating NS5A.
Cell Mol Immunol. 2016 Jan;13(1):94-102. doi: 10.1038/cmi.2014.131. Epub 2015 Feb 16.
4
Emerging roles of interferon-stimulated genes in the innate immune response to hepatitis C virus infection.
Cell Mol Immunol. 2016 Jan;13(1):11-35. doi: 10.1038/cmi.2014.127. Epub 2014 Dec 29.
5
MDA5 plays a critical role in interferon response during hepatitis C virus infection.
J Hepatol. 2015 Apr;62(4):771-8. doi: 10.1016/j.jhep.2014.11.007. Epub 2014 Nov 21.
6
Newly described pattern recognition receptors team up against intracellular pathogens.
Nat Rev Immunol. 2013 Aug;13(8):551-65. doi: 10.1038/nri3479. Epub 2013 Jul 12.
7
The E3-ligase TRIM family of proteins regulates signaling pathways triggered by innate immune pattern-recognition receptors.
Immunity. 2013 Feb 21;38(2):384-98. doi: 10.1016/j.immuni.2012.11.013.
8
TRIM22 inhibits influenza A virus infection by targeting the viral nucleoprotein for degradation.
J Virol. 2013 Apr;87(8):4523-33. doi: 10.1128/JVI.02548-12. Epub 2013 Feb 13.
9
Intrinsic antiviral immunity.
Nat Immunol. 2012 Feb 16;13(3):214-22. doi: 10.1038/ni.2229.
10
Regulation of innate immune signalling pathways by the tripartite motif (TRIM) family proteins.
EMBO Mol Med. 2011 Sep;3(9):513-27. doi: 10.1002/emmm.201100160. Epub 2011 Aug 9.
Zotero 插件