首页> 外文期刊>Biochemical and Biophysical Research Communications >A novel p38 mitogen activated protein kinase (MAPK) specific inhibitor suppresses respiratory syncytial virus and influenza A virus replication by inhibiting virus-induced p38 MAPK activation
【24h】

A novel p38 mitogen activated protein kinase (MAPK) specific inhibitor suppresses respiratory syncytial virus and influenza A virus replication by inhibiting virus-induced p38 MAPK activation

机译:一种新型的p38丝裂原活化蛋白激酶(MAPK)特异性抑制剂通过抑制病毒诱导的p38 MAPK活化来抑制呼吸道合胞病毒和甲型流感病毒复制

获取原文
获取原文并翻译 | 示例
           

摘要

Respiratory syncytial virus (RSV) and influenza A virus are leading causes of acute lower respiratory infectious disease. Respiratory diseases caused by RSV and influenza A virus result in serious economic burden and life-threatening disease for immunocompromised people. With the revelation that p38 mitogen-activated protein kinase (MAPK) activity in host cells is crucial for infection and replication of RSV and influenza A virus, inhibition of p38 MAPK activity has been suggested as a potential antiviral therapeutic strategy. However, the low selectivity and high toxicity of the p38 MAPK inhibitors necessitate the development of better inhibitors. Herein, we report the synthesis of a novel p38 MAPK inhibitor, NJK14047, with high kinase selectivity. In this work, it was demonstrated that NJK14047 inhibits RSV- and influenza A-mediated p38 MAPK activation in epithelial cells. Subsequently, NJK14047 treatment resulted in decreased viral replication and viral mRNA synthesis. In addition, secretion of interleukin-6 from infected cells was greatly diminished by NJK14047, suggesting that it can ameliorate immunopathological responses to RSV and influenza A. Collectively, the results suggest that NJK14047 has therapeutic potential to treat respiratory viral infection through the suppression of p38 MAPK activation, which is suggested to be an essential step for respiratory virus infection. (C) 2016 Elsevier Inc. All rights reserved.
机译:呼吸道合胞病毒(RSV)和A型流感病毒是急性下呼吸道感染性疾病的主要原因。 RSV和甲型流感病毒引起的呼吸道疾病给免疫受损的人带来了严重的经济负担和威胁生命的疾病。揭示宿主细胞中p38丝裂原活化蛋白激酶(MAPK)的活性对于RSV和甲型流感病毒的感染和复制至关重要,因此有人提出抑制p38 MAPK活性是一种潜在的抗病毒治疗策略。但是,p38 MAPK抑制剂的低选择性和高毒性需要开发更好的抑制剂。在本文中,我们报道了具有高激酶选择性的新型p38 MAPK抑制剂NJK14047的合成。在这项工作中,证明NJK14047抑制上皮细胞中RSV和甲型流感介导的p38 MAPK活化。随后,NJK14047处理导致病毒复制和病毒mRNA合成减少。此外,NJK14047大大减少了感染细胞中白细胞介素6的分泌,表明它可以改善对RSV和A型流感的免疫病理反应。总的来说,该结果表明NJK14047具有通过抑制p38来治疗呼吸道病毒感染的治疗潜力。 MAPK激活,这被认为是呼吸道病毒感染的重要步骤。 (C)2016 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号