| Literature DB >> 27226534 |
Luoquan Chen1, Yinjing Song1, Li He1, Xiaopeng Wan1, Lihua Lai1, Feng Dai1, Yang Liu2, Qingqing Wang3.
Abstract
Effective recognition of viral infection and subsequent triggering of antiviral innate immune responses are essential for the host antiviral defense, which is tightly regulated by multiple regulators, including microRNAs. Previous reports have shown that some microRNAs are induced during virus infection and participate in the regulation of the innate antiviral response. However, whether the type I IFN response is regulated by miR-223 is still unknown. Here, we reported that vesicular stomatitis virus (VSV) infection induced significant up-regulation of miR-223 in murine macrophages. We observed that miR-223 overexpression up-regulated type I IFN expression levels in VSV-infected macrophages. We also demonstrated that miR-223 directly targets FOXO3 to regulate the type I IFN production. Furthermore, type I IFN, which is triggered by VSV infection, is responsible for the up-regulation of miR-223, thus forming a positive regulatory loop for type I IFN production. Our results uncovered a novel mechanism of miR-223-mediated regulation of type I IFN production in the antiviral innate immunity for the first time.Entities:
Keywords: FOXO3; IRF7; antiviral agent; innate immunity; interferon; interferon regulatory factor (IRF); microRNA (miRNA); microRNA-223; type I interferon
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Year: 2016 PMID: 27226534 PMCID: PMC4938189 DOI: 10.1074/jbc.M115.700252
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157