Asian sand dust enhances murine lung inflammation caused by Klebsiella pneumoniae

被引:29
作者
He, Miao [2 ]
Ichinose, Takamichi [3 ]
Yoshida, Seiichi [3 ]
Yamamoto, Shoji [4 ]
Inoue, Ken-ichiro [4 ]
Takano, Hirohisa [4 ]
Yanagisawa, Rie [4 ]
Nishikawa, Masataka [5 ]
Mori, Ikuko [5 ]
Sun, Guifan [2 ]
Shibamoto, Takayuki [1 ]
机构
[1] Univ Calif Davis, Dept Environm Toxicol, Davis, CA 95616 USA
[2] China Med Univ, Dept Environm & Occupat Hlth, Coll Publ Hlth, Shenyang 11001, Peoples R China
[3] Oita Univ Nursing & Hlth Sci, Dept Hlth Sci, Oita 8701201, Japan
[4] Natl Inst Environm Studies, Pathophysiol Res Team, Tsukuba, Ibaraki 3058506, Japan
[5] Natl Inst Environm Studies, Div Environm Chem, Tsukuba, Ibaraki 3058506, Japan
关键词
Asian sand dust; Klebsiella pneumoniae; Lung inflammation; Toll-like receptor; NALP3; inflammasome; TOLL-LIKE RECEPTOR-2; DAILY MORTALITY; EXPRESSION; EVENTS; AIRWAY; STORM; HOSPITALIZATION; INFECTION; TRANSPORT; INCREASES;
D O I
10.1016/j.taap.2011.11.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Inhaling concomitants from Asian sand dust (ASD) may result in exacerbation of pneumonia by the pathogen. The exacerbating effect of ASD on pneumonia induced by Klebsiella pneumoniae 0(P) was investigated in ICR mice. The organic substances adsorbed onto ASD collected from the atmosphere of Iki-island in Japan were excluded by heat treatment at 360 degrees C for 30 min. ICR mice were instilled intratracheally with ASD at doses of 0.05 mg or 0.2 mg/mouse four times at 2-week intervals (total dose of 0.2 mg or 0.8 mg/mouse) and were administrated with ASD in the presence or absence of KP at the last intratracheal instillation. Pathologically, ASD caused exacerbation of pneumonia by KP as shown by increased inflammatory cells within the bronchiolar and the alveolar compartments. ASD enhanced the neutrophil number dose dependently as well as the expression of cytokines (IL-1 beta, IL-6, IL-12, IFN-gamma, TNE-alpha) and chemokines (KC, MCP-1, MIP-1 alpha) related to KP in BALF. In an in vitro study using RAW264.7 cells, combined treatment of ASD and KP increased gene expression of IL-1 beta, IL-6, IFN-beta, KC, MCP-1, and MIP-1 alpha. The same treatment tended to increase the protein level of IL-1 beta, TNE-alpha and MCP-1 in a culture medium compared to each treatment alone. The combined treatment tended to increase the gene expression of Toll-like receptor 2 (TLR2), and NALP3, ASC and caspase-1 compared with KP alone. These results suggest that the exacerbation of pneumonia by ASD + KP was due to the enhanced production of pro-inflammatory mediators via activation of TLR2 and NALP3 inflammasome pathways in alveolar macrophages. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:237 / 247
页数:11
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