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猪流行性腹泻病毒 ORF3 蛋白引起内质网应激以促进自噬。

Porcine epidemic diarrhea virus ORF3 protein causes endoplasmic reticulum stress to facilitate autophagy.

机构信息

College of Life Science and Technology, HeiLongJiang BaYi Agricultural University, Daqing 163319, China; Biotechnology Center, HeiLongJiang BaYi Agricultural University, Daqing 163319, China.

Branch of Animal Husbandry and Veterinary of HeiLongJiang Academy of Agricultural Sciences, Qiqihar, 161005, China.

出版信息

Vet Microbiol. 2019 Aug;235:209-219. doi: 10.1016/j.vetmic.2019.07.005. Epub 2019 Jul 8.

Abstract

Porcine epidemic diarrhea virus (PEDV), the causative agent of PED, is an enveloped, positive-stranded RNA virus in the genus Alphacoronavirus, family Coronaviridae, order Nidovirales. PEDV non-structural accessory protein ORF3 is an ion channel related to viral infectivity and pathogenicity. Our previous study showed that PEDV ORF3 has expression characteristic of aggregation in cytoplasm, but its biological function remains elusive. Thus in this study, we initiated the construction of various vectors to express ORF3, and found ORF3 localized in the cytoplasm in the aggregation manner. Subsequently, confocal microscopy analysis showed that the aggregated ORF3 localized in endoplasmic reticulum (ER) to trigger ER stress response via up-regulation of GRP78 protein expression and activation of PERK-eIF2α signaling pathway. In addition, our results showed that PEDV ORF3 could induce the autophagy through inducing conversion of LC3-I to LC3-II, but couldn't influence the apoptosis. In contrast, conversion of LC3-I/LC3-II could be significantly inhibited by 4-PBA, an ER stress inhibitor, indicating that ORF3-induced autophagy is dependent on ER stress response. This work not only provides some new findings for the biological function of the PEDV ORF3 protein, but also help us for the further understanding the molecular interaction between PEDV ORF3 protein and cells.

摘要

猪流行性腹泻病毒(PEDV)是引起猪流行性腹泻的病原体,属于冠状病毒科冠状病毒属的有包膜、正链 RNA 病毒。PEDV 的非结构辅助蛋白 ORF3 是一种与病毒感染力和致病性相关的离子通道。我们之前的研究表明,PEDV ORF3 在细胞质中有聚集表达的特征,但它的生物学功能仍不清楚。因此,在本研究中,我们开始构建各种载体来表达 ORF3,发现 ORF3 以聚集的方式定位于细胞质中。随后,共聚焦显微镜分析表明,聚集的 ORF3 定位于内质网(ER),通过上调 GRP78 蛋白表达和激活 PERK-eIF2α 信号通路来引发 ER 应激反应。此外,我们的结果表明,PEDV ORF3 可以通过诱导 LC3-I 向 LC3-II 的转化来诱导自噬,但不能影响细胞凋亡。相反,ER 应激抑制剂 4-PBA 可以显著抑制 LC3-I/LC3-II 的转化,表明 ORF3 诱导的自噬依赖于 ER 应激反应。这项工作不仅为 PEDV ORF3 蛋白的生物学功能提供了一些新的发现,还有助于我们进一步了解 PEDV ORF3 蛋白与细胞之间的分子相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77f/7117398/a945eeb199dc/gr1_lrg.jpg

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