转录因子
干扰素
病毒学
生物
细胞生物学
免疫学
癌症研究
遗传学
基因
作者
Tohru Kimura,Katsutoshi Nakayama,Josef Penninger,Motoo Kitagawa,Hisashi Harada,T. Matsuyama,Nobuyuki Tanaka,Ryutaro Kamijo,J Vilček,Tak W. Mak,Tadatsugu Taniguchi
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1994-06-24
卷期号:264 (5167): 1921-1924
被引量:309
标识
DOI:10.1126/science.8009222
摘要
The mechanisms underlying interferon (IFN)-induced antiviral states are not well understood. Interferon regulatory factor-1 (IRF-1) is an IFN-inducible transcriptional activator, whereas IRF-2 suppresses IRF-1 action. The inhibition of encephalomyocarditis virus (EMCV) replication by IFN-α and especially by IFN-γ was impaired in cells from mice with a null mutation in the IRF-1 gene (IRF-1 -/- mice). The IRF-1 -/- mice were less resistant than normal mice to EMCV infection, as revealed by accelerated mortality and a larger virus titer in target organs. The absence of IRF-1 did not clearly affect replication of two other types of viruses. Thus, IRF-1 is necessary for the antiviral action of IFNs against some viruses, but IFNs activate multiple activation pathways through diverse target genes to induce the antiviral state.
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