Haemophilus parasuis induces activation of NF-κB and MAP kinase signaling pathways mediated by toll-like receptors

被引:49
作者
Chen, Yushan [1 ]
Liu, Ting [1 ]
Langford, Paul [2 ]
Hua, Kexin [1 ]
Zhou, Shanshan [1 ]
Zhai, Yajun [1 ]
Xiao, Hongde [3 ]
Luo, Rui [1 ]
Bi, Dingren [1 ]
Jin, Hui [1 ]
Zhou, Rui [1 ]
机构
[1] Huazhong Agr Univ, Coll Vet Med, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
[2] Univ London Imperial Coll Sci Technol & Med, Paediat Sect, London W2 1PG, England
[3] Hubei Ctr Anim Dis Control & Prevent, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
Haemophilus parasuis; Inflammatory response; NF-kappa B pathway; MAPK pathway; TLRs; PK-15; CELLS; TRANSCRIPTION FACTORS; GLASSERS-DISEASE; PROTEIN-KINASES; SC096; STRAIN; INFECTION; EXPRESSION; IL-8; PIGS; TRANSDUCTION;
D O I
10.1016/j.molimm.2015.02.016
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
Glasser's disease in pigs caused by Haemophilus parasuis is characterized by a severe membrane inflammation. In our previous study, we have identified activation of the transcription factor NF-kappa B after H. parasuis infection of porcine epithelial cells. In this study, we found that H. parasuis infection also contributed to the activation of p38/JNK MAPK pathway predominantly linked to inflammation, but not the ERK MAPK pathway associated with growth, differentiation and development. Inhibition of NF-kappa B, p38 and JNK but not ERK activity significantly reduced IL-8 and CCL4 expression by H. parasuis. We also found TLR1, TLR2,TLR4 and TLR6 were required for NF-kappa B, p38 and JNK MAPK activation. Furthermore, MyD88 and TRIF signaling cascades were essential for H. parasuis-induced NF-kappa B activation. These results provided new insights into the molecular pathways underlying the inflammatory response induced by H. parasuis. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:360 / 366
页数:7
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