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606026 
Journal Article 
Inhaled asbestos exacerbates atherosclerosis in apolipoprotein E-deficient mice via CD4+ T cells 
Fukagawa, NK; Li, M; Sabo-Attwood, T; Timblin, CR; Butnor, KJ; Gagne, J; Steele, C; Taatjes, DJ; Huber, S; Mossman, BT 
2008 
Yes 
Environmental Health Perspectives
ISSN: 0091-6765
EISSN: 1552-9924 
116 
1218-1225 
English 
BACKGROUND: Associations between air pollution and morbidity/mortality from cardiovascular disease are recognized in epidemiologic and clinical studies, but the mechanisms by which inhaled fibers or particles mediate the exacerbation of atherosclerosis are unclear. OBJECTIVE AND METHODS: To determine whether lung inflammation after inhalation of a well-characterized pathogenic particulate, chrysotile asbestos, is directly linked to exacerbation of atherosclerosis and the mechanisms involved, we exposed apolipoprotein E--deficient (ApoE--/--) mice and ApoE--/-- mice crossed with CD4--/-- mice to ambient air, NIEHS (National Institute of Environmental Health Sciences) reference sample of chrysotile asbestos, or fine titanium dioxide (TiO2), a nonpathogenic control particle, for 3, 9, or 30 days. RESULTS: ApoE--/-- mice exposed to inhaled asbestos fibers had approximately 3-fold larger atherosclerotic lesions than did TiO2-exposed ApoE--/-- mice or asbestos-exposed ApoE--/--/CD4--/-- doubleknockout (DKO) mice. Lung inflammation and the magnitude of lung fibrosis assessed histologically were similar in asbestos-exposed ApoE--/-- and DKO mice. Monocyte chemoattractant protein-1 (MCP-1) levels were increased in bronchoalveolar lavage fluid and plasma, and plasma concentrations correlated with lesion size (p < 0.04) in asbestos-exposed ApoE--/-- mice. At 9 days, activator protein-1 (AP-1) and nuclear factor-κB (NF-κB), transcription factors linked to inflammation and found in the promoter region of the MCP-1 gene, were increased in aortas of asbestos-exposed ApoE--/-- but not DKO mice. CONCLUSION: Our findings show that the degree of lung inflammation and fibrosis does not correlate directly with cardiovascular effects of inhaled asbestos fibers and support a critical role of CD4+ T cells in linking fiber-induced... [ABSTRACT FROM AUTHOR] Copyright of Environmental Health Perspectives is the property of Superintendent of Documents and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts) 
CARDIOVASCULAR system -- Diseases; EPIDEMIOLOGY -- Research; INFLAMMATION; ATHEROSCLEROSIS; ASBESTOS; CHRYSOTILE; NATIONAL Institute of Environmental Health Sciences; GENETIC aspects; RISK factors; AP-1; CD4+; chrysotile asbestos; fibrosis; knockout mice; lung; MCP-1; NF-κB.; T-cells 
IRIS
• Asbestos
NAAQS
• ISA-Lead (2013 Final Project Page)
     Considered
OPPT REs
• OPPT_Asbestos, Part I: Chrysotile_C. Engineering
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• OPPT_Asbestos, Part I: Chrysotile_D. Exposure
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• OPPT_Asbestos, Part I: Chrysotile_E. Fate
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• OPPT_Asbestos, Part I: Chrysotile_F. Human Health
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• OPPT_Asbestos, Part I: Chrysotile_Supplemental Search
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