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牛病毒性腹泻病毒1型感染期间牛A20基因的过表达阻断了MDBK细胞中的NF-κB信号通路。

Bovine A20 gene overexpression during bovine viral diarrhea virus-1 infection blocks NF-κB pathway in MDBK cells.

作者信息

Villalba Melina, Canales Nivia, Maldonado Nicolas, Otth Carola, Fredericksen Fernanda, Garcés Pablo, Stepke Cristopher, Arriagada Valentina, Olavarría Víctor H

机构信息

Instituto de Bioquímica y Microbiología, Facultad de Ciencias, Laboratorio de Virología, Universidad Austral de Chile, Valdivia, Chile.

Instituto de Microbiología Clínica, Facultad de Medicina, Universidad Austral de Chile, Valdivia, Chile.

出版信息

Dev Comp Immunol. 2017 Dec;77:23-29. doi: 10.1016/j.dci.2017.07.019. Epub 2017 Jul 21.

Abstract

Viruses have developed cellular strategies to ensure progeny survival. One of the most interesting is immune camouflage, where the virus triggers a controlled-intensity immune response that prevents total destruction of the infected cell, thus "winning time" for the virus. This study explored the regulatory contexts of the bovine A20 gene during bovine viral diarrhea virus (BVDV)-1 infection, using IL-8 as an immune-response sentinel molecule. Assessments were conducted through RT-qPCR, Western blotting, gene silencing/overexpression, luciferase assays, and the use of pharmacological inhibitors, among other approaches. The results demonstrated that a) BVDV-1 increased A20 levels in Madin-Darby bovine kidney cells, b) increased A20 led to decreased IL-8 expression, and c) the virus affected the NF-κB signaling pathway. Collectively, these data identify bovine A20 as a strong regulator of immune marker expression. In conclusion, this is the first report on BVDV-1 modulating bovine IL-8 activation through the NF-κB/A20 pathway.

摘要

病毒已经发展出细胞策略来确保后代的存活。其中最有趣的一种是免疫伪装,即病毒引发一种强度可控的免疫反应,这种反应可防止被感染细胞被完全破坏,从而为病毒“赢得时间”。本研究以白细胞介素-8(IL-8)作为免疫反应的哨兵分子,探索了牛病毒性腹泻病毒1型(BVDV-1)感染期间牛A20基因的调控背景。通过逆转录定量聚合酶链反应(RT-qPCR)、蛋白质免疫印迹法、基因沉默/过表达、荧光素酶检测以及使用药理学抑制剂等方法进行评估。结果表明:a)BVDV-1可提高马-达二氏牛肾细胞中A20的水平;b)A20水平升高会导致IL-8表达降低;c)该病毒会影响核因子κB(NF-κB)信号通路。总体而言,这些数据表明牛A20是免疫标志物表达的强力调节因子。总之,这是关于BVDV-1通过NF-κB/A20途径调节牛IL-8激活的首份报告。

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