Biological factor related to Asian sand dust particles contributes to the exacerbation of asthma
| Autor: | Honda, Akiko, Sawahara, Takahiro, Hayashi, Tomohiro, Tsuji, Kenshi, Fukushima, Wataru, Oishi, Mizuki, Kitamura, Gaku, Kudo, Hitomi, Ito, Sho, Yoshida, Seiichi, Ichinose, Takamichi, Ueda, Kayo, Takano, Hirohisa |
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| Rok vydání: | 2016 |
| Předmět: |
Male
bone‐marrow‐derived antigen presenting cells Asia Antigen-Presenting Cells Dust Epithelial Cells Silicon Dioxide behavioral disciplines and activities Asthma Asian sand dust particles Mice mental disorders Benzo(a)pyrene Animals Cytokines Humans Bjerkandera adusta Polycyclic Aromatic Hydrocarbons Coriolaceae Spleen Cell Proliferation |
| Zdroj: | Journal of applied toxicology : JAT. 37(5) |
| ISSN: | 1099-1263 |
| Popis: | Epidemiologic studies have revealed that Asian sand dust particles (ASDs) can affect respiratory and immune health represented by asthma. Factors responsible for the exacerbation of asthma remain unclear. The fungus Bjerkandera adusta (B.ad) and polycyclic aromatic hydrocarbons such as benzo[a]pyrene (BaP) have been identified in ASDs collected from the atmosphere when an ASD event occurred. We investigated the effects of B.ad and BaP related to ASDs on respiratory and immune systems. Bone marrow-derived antigen-presenting cells (APCs) and splenocytes from atopic prone NC/Nga mice and human airway epithelial cells were exposed to the B.ad or to BaP in the presence and absence of heated-ASDs (H-ASDs). B.ad and BaP in both the presence and absence of H-ASDs increased the expression of cell surface molecules on APCs. H-ASDs alone slightly activated APCs. The expressions induced by B.ad were higher than those induced by BaP in the presence and absence of H-ASDs. There were no remarkable effects on the activation of splenocytes or the proinflammatory responses in airway epithelial cells. These results suggest that B.ad rather than BaP contributes to the exacerbation of asthma regardless of the presence or absence of sand particles, particularly by the activation of the immune system via APCs. Copyright © 2016 John WileySons, Ltd. |
| Databáze: | OpenAIRE |
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