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干扰素非依赖型非经典 STAT 激活与病毒诱导的炎症

Interferon Independent Non-Canonical STAT Activation and Virus Induced Inflammation.

机构信息

Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi 712100, China.

Molecular Virology Laboratory, VA-MD College of Veterinary Medicine and Maryland Pathogen Research Institute, University of Maryland, College Park, MD 20742, USA.

出版信息

Viruses. 2018 Apr 14;10(4):196. doi: 10.3390/v10040196.

Abstract

Interferons (IFNs) are a group of secreted proteins that play critical roles in antiviral immunity, antitumor activity, activation of cytotoxic T cells, and modulation of host immune responses. IFNs are cytokines, and bind receptors on cell surfaces to trigger signal transduction. The major signaling pathway activated by IFNs is the JAK/STAT (Janus kinase/signal transducer and activator of transcription) pathway, a complex pathway involved in both viral and host survival strategies. On the one hand, viruses have evolved strategies to escape from antiviral host defenses evoked by IFN-activated JAK/STAT signaling. On the other hand, viruses have also evolved to exploit the JAK/STAT pathway to evoke activation of certain STATs that somehow promote viral pathogenesis. In this review, recent progress in our understanding of the virus-induced IFN-independent STAT signaling and its potential roles in viral induced inflammation and pathogenesis are summarized in detail, and perspectives are provided.

摘要

干扰素 (IFNs) 是一组分泌蛋白,在抗病毒免疫、抗肿瘤活性、细胞毒性 T 细胞的激活以及宿主免疫反应的调节中发挥关键作用。IFNs 是细胞因子,与细胞表面的受体结合以触发信号转导。IFNs 激活的主要信号通路是 JAK/STAT(Janus 激酶/信号转导和转录激活因子)通路,这是一条复杂的通路,涉及病毒和宿主的生存策略。一方面,病毒已经进化出逃避由 IFN 激活的 JAK/STAT 信号引发的抗病毒宿主防御的策略。另一方面,病毒也进化出利用 JAK/STAT 通路来引发某些 STAT 的激活,这些 STAT 以某种方式促进病毒发病机制。在这篇综述中,详细总结了我们对病毒诱导的 IFN 非依赖性 STAT 信号及其在病毒诱导的炎症和发病机制中的潜在作用的最新理解方面的进展,并提供了一些观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0e8/5923490/a862d3948bab/viruses-10-00196-g001.jpg

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