Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/33032
標題: Mechanisms underlying Actinobacillus pleuropneumoniae exotoxin ApxI induced expression of IL-1 beta, IL-8 and TNF-alpha in porcine alveolar macrophages
作者: Chen, Zeng-Weng
Chien, Maw-Sheng
Chang, Nai-Yun
Chen, Ter-Hsin
Wu, Chi-Ming
Huang, Chienjin
Lee, Wei-Cheng
Hsuan, Shih-Ling
關鍵字: pasteurella-haemolytica leukotoxin
activated protein-kinase
nf-kappa-b
gene-expression
rtx toxins
inflammatory cytokines
c-jun
signaling pathways
calcium elevation
bovine leukocytes
摘要: Actinobacillus pleuropneumoniae (A. pleuropneumoniae) causes fibrino-hemorrhagic necrotizing pleuropneumonia in pigs. Production of proinflammatory mediators in the lungs is an important feature of A. pleuropneumoniae infection. However, bacterial components other than lipopolysaccharide involved in this process remain unidentified. The goals of this study were to determine the role of A. pleuropneumoniae exotoxin ApxI in cytokine induction and to delineate the underlying mechanisms. Using real-time quantitative PCR analysis, we found native ApxI stimulated porcine alveolar macrophages (PAMs) to transcribe mRNAs of IL-1 beta, IL-8 and TNF-alpha in a concentration-and time-dependent manner. Heat-inactivation or pre-incubation of ApxI with a neutralizing antiserum attenuated ApxI bioactivity to induce cytokine gene expression. The secretion of IL-1 beta, IL-8 and TNF-alpha protein from PAMs stimulated with ApxI was also confirmed by quantitative ELISA. In delineating the underlying signaling pathways contributing to cytokine expression, we observed mitogen-activated protein kinases (MAPKs) p38 and cJun NH2-terminal kinase (JNK) were activated upon ApxI stimulation. Administration of an inhibitor specific to p38 or JNK resulted in varying degrees of attenuation on ApxI-induced cytokine expression, suggesting the differential regulatory roles of p38 and JNK in IL-1 beta, IL-8 and TNF-alpha production. Further, pre-incubation of PAMs with a CD18-blocking antibody prior to ApxI stimulation significantly reduced the activation of p38 and JNK, and subsequent expression of IL-1 beta, IL-8 or TNF-alpha gene, indicating a pivotal role of beta 2 integrins in the ApxI-mediated effect. Collectively, this study demonstrated ApxI induces gene expression of IL-1 beta, IL-8 and TNF-alpha in PAMs that involves beta 2 integrins and downstream MAPKs.
URI: http://hdl.handle.net/11455/33032
ISSN: 0928-4249
Appears in Collections:獸醫病理生物學所

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