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

被引:36
|
作者
Choi, Myung-Soo [1 ]
Heo, Jinyuk [2 ]
Yi, Chae-Min [1 ]
Ban, Junsu [1 ]
Lee, Noh-Jin [1 ]
Lee, Na-Rae [1 ]
Kim, Sang Won [2 ]
Kim, Nam-Jung [2 ]
Inn, Kyung-Soo [1 ]
机构
[1] Kyung Hee Univ, Dept Pharmaceut Sci, Coll Pharm, 26 Kyungheedae Ro, Seoul 02447, South Korea
[2] Kyung Hee Univ, Dept Pharm, Coll Pharm, 26 Kyungheedae Ro, Seoul 02447, South Korea
基金
新加坡国家研究基金会;
关键词
p38 mitogen activated protein kinase; Respiratory syncytial virus; Influenza A virus; Antiviral agent; INFECTION; CHILDREN; PATHWAY;
D O I
10.1016/j.bbrc.2016.06.111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
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页码:311 / 316
页数:6
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