Suppr超能文献

麻疹病毒激活人肺上皮细胞系A549中的核因子-κB和信号转导及转录激活因子转录因子,并诱导α/β干扰素和白细胞介素-6的产生。

Measles virus activates NF-kappa B and STAT transcription factors and production of IFN-alpha/beta and IL-6 in the human lung epithelial cell line A549.

作者信息

Helin E, Vainionpää R, Hyypiä T, Julkunen I, Matikainen S

机构信息

Department of Virology, University of Turku, Kiinamyllynkatu 13, FIN-20520 Turku, Finland.

出版信息

Virology. 2001 Nov 10;290(1):1-10. doi: 10.1006/viro.2001.1174.

Abstract

Epithelial cells of the respiratory tract are the primary targets of measles virus (MV) infection. In this work we have studied the effect of MV infection on the activation of transcription factors nuclear factor (NF)-kappa B and signal transducer and activator of transcription (STAT) and the production of cytokines in the lung epithelial A549 cell line. NF-kappa B and STAT activation were induced by MV in A549 cells as analyzed by electrophoretic mobility shift assay. NF-kappa B activation was rapid and it was not inhibited by the protein synthesis inhibitor cycloheximide, suggesting that MV directly activates NF-kappa B. In contrast, Stat1, Stat3, and interferon-stimulated gene factor 3 (ISGF3) DNA binding was induced by MV infection with delayed kinetics compared to NF-kappa B activation. MV infection also resulted in an efficient interferon (IFN)-alpha/beta and interleukin-6 production. Cycloheximide and neutralizing anti-IFN-alpha/beta antibodies inhibited MV-induced activation of Stat1, Stat3, and ISGF3 DNA binding in A549 cells. In conclusion, the results suggest that MV infection activates transcription factors involved in the initiation of innate immune responses in epithelial cells by two different mechanisms: directly by leading to NF-kappa B activation and indirectly via IFN-alpha/beta leading to STAT activation.

摘要

呼吸道上皮细胞是麻疹病毒(MV)感染的主要靶标。在本研究中,我们研究了MV感染对肺上皮A549细胞系中转录因子核因子(NF)-κB和信号转导及转录激活因子(STAT)的激活以及细胞因子产生的影响。通过电泳迁移率变动分析可知,MV在A549细胞中诱导了NF-κB和STAT的激活。NF-κB的激活迅速,且不受蛋白质合成抑制剂环己酰亚胺的抑制,这表明MV直接激活NF-κB。相比之下,与NF-κB激活相比,MV感染以延迟动力学诱导Stat1、Stat3和干扰素刺激基因因子3(ISGF3)的DNA结合。MV感染还导致高效的干扰素(IFN)-α/β和白细胞介素-6的产生。环己酰亚胺和中和抗IFN-α/β抗体抑制了MV诱导的A549细胞中Stat1、Stat3和ISGF3的DNA结合。总之,结果表明MV感染通过两种不同机制激活上皮细胞中参与先天免疫反应起始的转录因子:直接导致NF-κB激活,间接通过IFN-α/β导致STAT激活。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验