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呼吸道上皮细胞中腺病毒介导的天然免疫的新见解

New Insights to Adenovirus-Directed Innate Immunity in Respiratory Epithelial Cells.

作者信息

Carlin Cathleen R

机构信息

Department of Molecular Biology and Microbiology and the Case Comprehensive Cancer Center, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.

出版信息

Microorganisms. 2019 Jul 25;7(8):216. doi: 10.3390/microorganisms7080216.

Abstract

The nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) family of transcription factors is a key component of the host innate immune response to infectious adenoviruses and adenovirus vectors. In this review, we will discuss a regulatory adenoviral protein encoded by early region 3 (E3) called E3-RIDα, which targets NFκB through subversion of novel host cell pathways. E3-RIDα down-regulates an EGF receptor signaling pathway, which overrides NFκB negative feedback control in the nucleus, and is induced by cell stress associated with viral infection and exposure to the pro-inflammatory cytokine TNF-α. E3-RIDα also modulates NFκB signaling downstream of the lipopolysaccharide receptor, Toll-like receptor 4, through formation of membrane contact sites controlling cholesterol levels in endosomes. These innate immune evasion tactics have yielded unique perspectives regarding the potential physiological functions of host cell pathways with important roles in infectious disease.

摘要

活化B细胞核因子κB轻链增强子(NFκB)转录因子家族是宿主对感染性腺病毒和腺病毒载体先天性免疫反应的关键组成部分。在本综述中,我们将讨论由早期区域3(E3)编码的一种调节性腺病毒蛋白,称为E3-RIDα,它通过颠覆新的宿主细胞途径靶向NFκB。E3-RIDα下调表皮生长因子受体信号通路,该通路在细胞核中凌驾于NFκB负反馈控制之上,并由与病毒感染和暴露于促炎细胞因子TNF-α相关的细胞应激诱导。E3-RIDα还通过形成控制内体胆固醇水平的膜接触位点,调节脂多糖受体Toll样受体4下游的NFκB信号传导。这些先天性免疫逃避策略为宿主细胞途径在传染病中发挥重要作用的潜在生理功能提供了独特的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa9f/6723309/fc98526f9d57/microorganisms-07-00216-g002.jpg

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