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Inhalation Toxicology
International Forum for Respiratory Research
Volume 30, 2018 - Issue 11-12
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Research Article

Source-apportioned coarse particulate matter exacerbates allergic airway responses in mice

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Pages 405-415 | Received 14 Aug 2018, Accepted 25 Oct 2018, Published online: 05 Dec 2018
 

Abstract

Exposure to coarse particulate matter (PM) is associated with lung inflammation and exacerbation of respiratory symptoms in sensitive populations, but the degree to which specific emission sources contribute to these effects is unclear. We examined whether coarse PM samples enriched with diverse sources differentially exacerbate allergic airway responses. Coarse PM was collected weekly (7/2009–6/2010) from urban (G.T. Craig [GTC]) and rural (Chippewa Lake Monitor [CLM]) sites in the Cleveland, Ohio area. Source apportionment results were used to pool GTC filter PM extracts into five samples dominated by traffic, coal, steel (two samples), or road salt sources. Five CLM samples were prepared from corresponding weeks. Control non-allergic and house dust mite (HDM)-allergic Balb/cJ mice were exposed by oropharyngeal aspiration to 100 μg coarse GTC or CLM, control filter extract, or saline only, and responses were examined 2 d after PM exposures. In allergic mice, CLM traffic, CLM road salt and all GTC samples except steel-1 significantly increased airway responsiveness to methacholine (MCh) compared with control treatments. In non-allergic mice, CLM traffic, CLM steel-2 and all GTC samples except coal significantly increased bronchoalveolar lavage fluid (BALF) neutrophils, while only CLM traffic PM increased eosinophils in allergic mice. In non-allergic mice, CLM coal PM increased BALF interleukin (IL)-13 and GTC steel-1 PM increased TNF-α levels. These results demonstrate that equal masses of GTC and CLM coarse PM enriched with a variety of sources exacerbate allergic airway disease. Greater PM concentrations at the urban GTC site signify a greater potential for human health effects.

Acknowledgments

The authors thank Debora Andrews, Lisa Copeland, Janice Dye, Rachel Grindstaff, Richard Jaskot, Kasey Kovalcik, William Padgett, Bakul Patel, Judy Richards and Samantha Snow for their technical assistance. Drs. Urmila Kodavanti and Erin Hines provided critical reviews of the manuscript.

Disclosure statement

The authors declare no conflicts of interest.

Disclaimer

The research described in this article has been reviewed by the National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency and approved for publication. Approval does not signify that the contents necessarily reflect the views or the policies of the Agency nor does mention of trade names or commercial products constitute endorsement or recommendation for use.

Additional information

Funding

M.M.H. was supported by interagency agreement #92429801 with the Oak Ridge Institute for Science and Education.

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