The immunomodulatory effects of diesel exhaust particles in asthma

被引:9
|
作者
de Homdedeu, M. [1 ,2 ,3 ]
Cruz, M. J. [1 ,2 ,3 ]
Sanchez-Diez, S. [1 ,2 ,3 ]
Ojanguren, I [1 ,2 ,3 ]
Romero-Mesones, C. [1 ,2 ,3 ]
Vanoirbeek, J. [5 ]
Velde, Vande G. [6 ]
Munoz, X. [1 ,2 ,3 ,4 ]
机构
[1] Hosp Univ Vall dHebron, Pulmonol Serv, Barcelona, Spain
[2] CIBER Enfermedades Resp CibeRes, Barcelona, Spain
[3] Univ Autonoma Barcelona, Med Dept, Barcelona, Spain
[4] Univ Autonoma Barcelona, Dept Cell Biol Physiol & Immunol, Barcelona, Spain
[5] Katholieke Univ Leuven, Ctr Environm & Hlth, Leuven, Belgium
[6] Katholieke Univ Leuven, Dept Imaging & Pathol, Biomed MRI, Mol Small Anim Imaging Ctr MoSAIC, Leuven, Belgium
关键词
Occupational asthma; Air pollution; Persulfate salts; Dendritic cells; Particle deposition; OUTDOOR AIR-POLLUTION; OCCUPATIONAL ASTHMA; ADJUVANT ACTIVITY; DENDRITIC CELLS; PERSULFATE; IGE; INDUCTION; EXPOSURE; INITIATE;
D O I
10.1016/j.envpol.2020.114600
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ammonium persulfate (AP) causes occupational asthma (OA) and diesel exhaust particles (DEP) exacerbate asthma; however, the role of DEP in asthma due to chemical agents has not been assessed to date. Therefore, the present work aims to study the immunomodulatory effects of DEP in a mouse model of chemical asthma. BALB/c ByJ mice were randomly divided into four experimental groups. On days 1 and 8, mice were dermally sensitized with AP or saline. On days 15, 18 and 21, they received intranasal instillations of AP or saline. Two experimental groups received DEP on every of the three challenges. Airway hyperresponsiveness (AHR), lung mechanics, pulmonary inflammation in bronchoalveolar lavage, leukocyte numbers in total lung tissue, oxidative stress and optical projection tomography (OPT) studies were assessed. The AP-sensitized and challenged group showed asthma-like responses, such as airway hyperresponsiveness, increased levels of eosinophils and NKs and lower numbers of monocytes and CD11b-Ly6C- dendritic cells (DCs). Mice exposed to DEP alone showed increased levels of neutrophils and NKs, reduced numbers of monocytes and alveolar macrophages, and increased levels of CD11b thorn Ly6CDCs. The AP sensitized and AP thorn DEP challenged group also showed asthma-like symptoms such as AHR, as well as increased numbers of eosinophils, neutrophils, CD11b thorn Ly6C- DCs and decreased levels of total and alveolar macrophages and tolerogenic DCs. Particle deposition was visualised using OPT. In the DEP group the particles were distributed relatively evenly, while in the AP thorn DEP group they were seen mainly in the large conducting airways. The results show that DEP exposure activates the innate immune response and, together with AP, exacerbates asthma immune hallmarks. This mouse model provides the first evidence of the capacity of DEPs to increase CD11b thorn Ly6C- (Th2-related) DCs. This study also demonstrates, for the first time, a differential deposition pattern of DEP in lungs depending on asthma status. (c) 2020 Elsevier Ltd. All rights reserved.
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页数:9
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