Activation of Pulmonary Dendritic Cells and Th2-Type Inflammatory Responses on Instillation of Engineered, Environmental Diesel Emission Source or Ambient Air Pollutant Particles in vivo

被引:47
作者
Bezemer, Gillina F. G. [1 ]
Bauer, Stephen M. [2 ]
Oberdoerster, Guenter [3 ,5 ]
Breysse, Patrick N. [6 ]
Pieters, Raymond H. H. [1 ]
Georas, Steve N. [2 ,4 ,5 ]
Williams, Marc A. [2 ,4 ,5 ]
机构
[1] Univ Utrecht, Immunotoxicol Inst Risk Assessment Sci, Utrecht, Netherlands
[2] Univ Rochester, Sch Med & Dent, Div Pulm & Crit Care Med, Rochester, NY USA
[3] Univ Rochester, Sch Med & Dent, Div Resp Biol & Toxicol, Rochester, NY USA
[4] Univ Rochester, Sch Med & Dent, Lung Biol & Dis Program, Rochester, NY USA
[5] Univ Rochester, Sch Med & Dent, Dept Environm Med, Rochester, NY USA
[6] Johns Hopkins Univ, Dept Environm Hlth Sci, Bloomberg Sch Publ Hlth, Baltimore, MD 21205 USA
基金
美国国家环境保护局;
关键词
Innate immunity; Allergic immunity; Dendritic cell; Lung; Inflammation; Immunotoxicology; Toxicology; Particulate matter; Nanoparticles; EXHAUST PARTICLES; METABOLIC PATHWAYS; OXIDATIVE STRESS; PM2.5; COMPONENTS; INHALED ANTIGEN; T-CELLS; IMMUNE; ULTRAFINE; ADJUVANT; RELEASE;
D O I
10.1159/000321725
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The biological effects of acute particulate air pollution exposure in host innate immunity remain obscure and have relied largely on in vitro models. We hypothesized that single acute exposure to ambient or engineered particulate matter (PM) in the absence of other secondary stimuli would activate lung dendritic cells (DC) in vivo and provide information on the early immunological events of PM exposure and DC activation in a mouse model naive to prior PM exposure. Activation of purified lung DC was studied following oropharyngeal instillation of ambient particulate matter (APM). We compared the effects of APM exposure with that of diesel-enriched PM (DEP), carbon black particles (CBP) and silver nanoparticles (AgP). We found that PM species induced variable cellular infiltration in the lungs and only APM exposure induced eosinophilic infiltration. Both APM and DEP activated pulmonary DC and promoted a Th2-type cytokine response from naive CD4+T cells ex vivo. Cultures of primary peribronchial lymph node cells from mice exposed to APM and DEP also displayed a Th2-type immune response ex vivo. We conclude that exposure of the lower airway to various PM species induces differential immunological responses and immunomodulation of DC subsets. Environmental APM and DEP activated DC in vivo and provoked a Th2 response ex vivo. By contrast, CBP and AgP induced altered lung tissue barrier integrity but failed to stimulate CD4+T cells as effectively. Our work suggests that respirable pollutants activate the innate immune response with enhanced DC activation, pulmonary inflammation and Th2-immune responsiveness. Copyright (c) 2010 S. Karger AG, Basel
引用
收藏
页码:150 / 166
页数:17
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