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MCPIP1 通过靶向病毒 RNA 抑制柯萨奇病毒 B3 的复制,并负调控病毒诱导的炎症反应。

MCPIP1 inhibits coxsackievirus B3 replication by targeting viral RNA and negatively regulates virus-induced inflammation.

机构信息

Institute of Biology and Medical Sciences, Soochow University, Building 703, 199 Ren-ai Road, Suzhou, 215123, China.

出版信息

Med Microbiol Immunol. 2018 Feb;207(1):27-38. doi: 10.1007/s00430-017-0523-0. Epub 2017 Oct 17.

Abstract

Monocyte chemotactic protein-induced protein 1(MCPIP1) is identified as an important inflammatory regulator during immune response. MCPIP1 possesses antiviral activities against several viruses, such as Japanese encephalitis. However, its role on Coxsackievirus B3 (CVB3) infection, a positive-stranded RNA virus, has not been addressed. Here, we reported that MCPIP1 was up-regulated in cardiomyocytes by CVB3 infection and in hearts and pancreas of infected mice. Then we found that overexpression of MCPIP1 inhibited CVB3 replication and knockdown of it promoted virus replication. Luciferase assay demonstrated MCPIP1 targeting non-ARE region of CVB3 3'UTR, which was dependent on its RNase, RNA binding and oligomerization abilities, but not deubiquitinase activity. We further verified that MCPIP1 negatively regulated CVB3-induced inflammatory response in macrophages. Thus, our data suggest MCPIP1 as a potent host defense against CVB3 infection and viral myocarditis.

摘要

单核细胞趋化蛋白诱导蛋白 1(MCPIP1)被鉴定为免疫反应过程中的一种重要炎症调节因子。MCPIP1 具有针对多种病毒的抗病毒活性,例如日本脑炎病毒。然而,它在柯萨奇病毒 B3(CVB3)感染中的作用,一种正链 RNA 病毒,尚未得到解决。在这里,我们报道了 CVB3 感染可使心肌细胞中 MCPIP1 上调,并且在感染小鼠的心脏和胰腺中也是如此。然后我们发现,MCPIP1 的过表达可抑制 CVB3 的复制,而敲低则可促进病毒复制。荧光素酶测定表明 MCPIP1 靶向 CVB3 3'UTR 的非 ARE 区域,这依赖于其核糖核酸酶、RNA 结合和寡聚化能力,但不依赖于去泛素化酶活性。我们进一步验证了 MCPIP1 可负调控巨噬细胞中 CVB3 诱导的炎症反应。因此,我们的数据表明 MCPIP1 是针对 CVB3 感染和病毒性心肌炎的有效宿主防御机制。

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