MicroRNA-218 inhibits type I interferon production and facilitates virus immune evasion via targeting RIG-I

التفاصيل البيبلوغرافية
العنوان: MicroRNA-218 inhibits type I interferon production and facilitates virus immune evasion via targeting RIG-I
المؤلفون: Yongle Qiu, Yuanhang Liu, Jiandong Ban, Xixue Geng
المصدر: Biotechnology and applied biochemistryReferences. 67(3)
سنة النشر: 2019
مصطلحات موضوعية: 0106 biological sciences, Male, viruses, Biomedical Engineering, Bioengineering, Microbial Sensitivity Tests, Biology, 01 natural sciences, Applied Microbiology and Biotechnology, Antiviral Agents, Virus, 03 medical and health sciences, Mice, Immune system, 010608 biotechnology, Drug Discovery, microRNA, Animals, Gene, Cells, Cultured, 030304 developmental biology, Immune Evasion, 0303 health sciences, RIG-I, Process Chemistry and Technology, Macrophages, General Medicine, Vesiculovirus, Evasion (ethics), Type I interferon production, Cell biology, Mice, Inbred C57BL, MicroRNAs, Interferon Type I, Molecular Medicine, DEAD Box Protein 58, Signal transduction, Biotechnology
الوصف: The host protective immunity against viral infection requires the effective detection of viral antigens and the subsequent production of type I interferons (IFNs) by host immune cells. Retinoic acid-inducible gene I (RIG-I) is the crucial signaling element responsible for sensing viral RNA component and initiating the downstream antiviral signaling pathways, leading to the production of type I IFNs. In this work, we identified microRNA-218 (miR-218) as a new virus-induced miRNA that dampens the expression of RIG-I in mouse and human macrophages, leading to the impaired production of type I IFNs. Interfering miR-218 expression rescued RIG-I-mediated antiviral signaling and thus protected macrophages from viral infection. Hence, our results provide new understanding of miRNA-mediated viral immune evasion and may be potentially useful for the treatment of viral infection in the future.
تدمد: 1470-8744
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49d799c492d510dfd79dc2e4360caf9dTest
https://pubmed.ncbi.nlm.nih.gov/31912548Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....49d799c492d510dfd79dc2e4360caf9d
قاعدة البيانات: OpenAIRE