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呼吸道合胞病毒非结构蛋白 1 通过 miR-19a-3p 促进 5-脂氧合酶。

Respiratory Syncytial Virus Nonstructural Protein 1 Promotes 5-Lipoxygenase via miR-19a-3p.

机构信息

Department of Pediatrics, Children's Digital Health and Data Center, Zhongnan Hospital of Wuhan University, Wuhan, China.

出版信息

J Immunol Res. 2022 May 20;2022:4086710. doi: 10.1155/2022/4086710. eCollection 2022.

Abstract

BACKGROUND

Respiratory syncytial virus (RSV) infection can regulate the expression of a wide range of noncoding microRNAs (miRNAs), in which mir-19a-3p can participate in airway inflammatory response by regulating 5-lipoxygenase (5-LO) pathway. RSV nonstructural protein (NS) 1 is involved in the airway hyperresponsiveness during RSV infection.

METHODS

The expression levels of miR-19a-3p and inflammatory signaling-related indicators were detected using quantitative real-time PCR and western blot analyses on the A549 cells transfected with NS1 expression plasmids (pNS1). The 5-LO-mediated inflammatory signaling pathway was assessed when the miR-19a-3p or 5-LO was inhibited.

RESULTS

The immunofluorescence analysis showed that the plasmid-mediated NS1 protein was observed in both the cytoplasm and nucleus. The expression level of miR-19a-3p was significantly upregulated in the pNS1 or RSV-treated cells, which was reversed by the NS1 small interfering RNA. In addition, pNS1 also upregulated the expression of 5-LO, interleukin-5 (IL-5), and leukotriene B (LTB), which was also significantly inhibited by the miR-19a-3p antagonists. The 5-LO inhibitor MK886 prevented the increase in the expression level of IL-5 induced by pNS1.

CONCLUSIONS

These results suggested that the RSV NS1 might play an important role in the pathogenesis of RSV by activating the 5-LO and subsequent inflammatory cytokines through miR-19a-3p.

摘要

背景

呼吸道合胞病毒(RSV)感染可以调节广泛的非编码 microRNAs(miRNAs)的表达,其中 mir-19a-3p 可以通过调节 5-脂氧合酶(5-LO)途径参与气道炎症反应。RSV 非结构蛋白(NS)1 参与 RSV 感染期间的气道高反应性。

方法

通过定量实时 PCR 和 Western blot 分析转染 NS1 表达质粒(pNS1)的 A549 细胞,检测 miR-19a-3p 和炎症信号相关指标的表达水平。当抑制 miR-19a-3p 或 5-LO 时,评估 5-LO 介导的炎症信号通路。

结果

免疫荧光分析显示,质粒细胞和核内均观察到质粒介导的 NS1 蛋白。pNS1 或 RSV 处理的细胞中 miR-19a-3p 的表达水平显著上调,NS1 小干扰 RNA 可逆转该上调。此外,pNS1 还上调了 5-LO、白细胞介素 5(IL-5)和白三烯 B(LTB)的表达,miR-19a-3p 拮抗剂也显著抑制了它们的表达。5-LO 抑制剂 MK886 可防止 pNS1 诱导的 IL-5 表达水平升高。

结论

这些结果表明,RSV NS1 可能通过激活 5-LO 和随后的炎症细胞因子通过 miR-19a-3p 发挥重要作用,从而导致 RSV 的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e422/9146443/e298b6a5d8f4/JIR2022-4086710.001.jpg

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