| Literature DB >> 33670458 |
Yeon-Su Lee1, Xiaoyong Bao2, Hwi-Ho Lee3, Jiyoung Joan Jang3, Enkhjin Saruuldalai3, Gaeul Park1, Wonkyun Ronny Im3,4, Jong-Lyul Park5,6, Seon-Young Kim5,6, Sooyong Shin4, Sung Ho Jeon4, Sangmin Kang3, Hyun-Sung Lee7, Ju-Seog Lee8, Ke Zhang2, Eun Jung Park3, In-Hoo Kim3, Yong Sun Lee3.
Abstract
Interferons (IFNs) are a crucial component in the innate immune response. Especially the IFN-β signaling operates in most cell types and plays a key role in the first line of defense upon pathogen intrusion. The induction of IFN-β should be tightly controlled, because its hyperactivation can lead to tissue damage or autoimmune diseases. Activation of the IFN-β promoter needs Interferon Regulatory Factor 3 (IRF3), together with Nuclear Factor kappa-light-chain-enhancer of activated B cells (NF-κB) and Activator Protein 1 (AP-1). Here we report that a human noncoding RNA, nc886, is a novel suppressor for the IFN-β signaling and inflammation. Upon treatment with several pathogen-associated molecular patterns and viruses, nc886 suppresses the activation of IRF3 and also inhibits NF-κB and AP-1 via inhibiting Protein Kinase R (PKR). These events lead to decreased expression of IFN-β and resultantly IFN-stimulated genes. nc886's role might be to restrict the IFN-β signaling from hyperactivation. Since nc886 expression is regulated by epigenetic and environmental factors, nc886 might explain why innate immune responses to pathogens are variable depending on biological settings.Entities:
Keywords: Interferon Regulatory Factor 3; Protein Kinase R; interferon; nc886; pathogen
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Year: 2021 PMID: 33670458 PMCID: PMC7922379 DOI: 10.3390/ijms22042003
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923