Andrographolide exerted its antimicrobial effects by upregulation of human β-defensin-2 induced through p38 MAPK and NF-κB pathway in human lung epithelial cells

被引:0
|
作者
Shao, Zhen-Jun [1 ]
Zheng, Xiao-Wei [2 ,3 ]
Feng, Ting [1 ]
Huang, Juan [1 ]
Chen, Jian [3 ]
Wu, Yi-Ying [3 ]
Zhou, Li-Ming [3 ]
Tu, Wen-Wei [1 ]
Li, Hong [1 ]
机构
[1] Sichuan Univ, Lab Joint Res Ctr WCSUH & UHK, Key Lab Obstetr & Gynecol & Pediat Dis & Birth De, Minist Educ,W China Univ Hosp 2, Chengdu 610041, Peoples R China
[2] Zhejiang Canc Hosp, Hangzhou 310022, Zhejiang, Peoples R China
[3] Sichuan Univ, Dept Pharmacol, Preclin & Forens Med Coll, Chengdu 610041, Peoples R China
关键词
andrographolide; defensin; beta-defensin; hBD-2; MAPKs; p38; MAPK; antimicrobial; NF-kappa B; SIGNALING PATHWAY; A549; CELLS; PANICULATA; EXPRESSION; INVOLVEMENT; DEFENSINS; JNK; INFECTIONS; INDUCTION; MULTIPLE;
D O I
10.1139/Y2012-050
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Andrographis paniculata (Burm. f) Nees is a traditional herbal medicine for the treatment of infection and inflammation in China. Andrographolide (andro) is one of the major components. Human beta-defensin-2 (hBD-2) is an inducible antimicrobial peptide that plays an important role in innate immunity. The present study aimed to investigate the effect of andro on upregulation of hBD-2 and the key signaling pathways involved in andro-induced hBD-2 expression. Real-time reverse transcription - PCR and Western blot assays showed that andro (1.0-10 mu mol/L) can upregulate the expression of hBD-2 in a dose-dependent manner. Further studies suggested that hBD-2 mRNA and protein expression in responsive to andro were attenuated by pretreatment with SB203580 (an inhibitor of p38 mitogen-activated protein kinase (p38 MAPK)), MG-132 (an inhibitor of nuclear factor kappa B (NF-kappa B)), and an NF-kappa B activator inhibitor, but not by an inhibitor of ERK (PD98059) or by an inhibitor of JNK(SP600125). Moreover, we found that a second p38 MAPK inhibitor (SB202190) significantly blocked andro-mediated hBD-2 induction in SPC-A-1 lung epithelial cells. Finally, the p-c-Jun transcription factor activity assay also showed that AP-1 activity was induced by andro compared with the untreated group. We conclude that andro may exert its antimicrobial effects by upregulating the expression of hBD-2 through the p38 MAPK and NF-kappa B pathway.
引用
收藏
页码:647 / 653
页数:7
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