The overall goal of the Animal Exposure and Assessment Core is to provide support to investigators studying the impact of oxidant air pollutants on allergic airways disease in infant rhesus monkeys. The Core is housed in the Exposure Facility at the California National Primate Research Center (CNPRC). Our Program Project team has recently established a non-human primate model of allergic airways disease that closely matches human infant allergic airways disease. Our model is generated in rhesus monkeys using a known human allergen, the house dust mite (HDM;Dermatophagoides famiae). We have found that ozone (O3) co-exposure markedly enhances the disease. The Exposure Facility at the CNPRC has well-established facilities for assessing all aspects of airways reactivity, immune response, and exposure to allergens and oxidant gases with validated exposure conditions, and it has a complete pulmonary function testing unit. Specifically, this Core will: 1. Provide accurate and carefully controlled exposures of animals or in vitro preparations to selected types and concentrations of air pollutants. 2. Develop methods of inhalation exposure and atmosphere characterization. 3. Coordinate the purchase, health services, and care of experimental animals. 4. Provide logistical and technical support to ensure the correct implementation of experimental regimens. 5. Prepare HDM allergen for use in sensitization and challenge of infant rhesus monkeys. 6. Sensitize infant rhesus monkeys to HDM allergen using a published protocol developed by our group. 7. Verify sensitization to HDM allergen using skin prick tests. 8. Provide researchers with infant rhesus monkeys with carefully defined allergic airways disease using carefully controlled and validated exposure conditions for oxidant gases and HDM allergen. 9. Provide carefully documented status of airway responsiveness and lung mechanics and volumes in infant rhesus monkeys. 10. Collate all exposure, sensitization, and pulmonary function data and provide this to the experimental units. 11. Coordinate the acquisition of tissues at necropsy and maintain the collection archive and sample custody and storage log.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Program Projects (P01)
Project #
5P01ES000628-36
Application #
8069609
Study Section
Special Emphasis Panel (ZES1)
Project Start
Project End
Budget Start
2010-05-01
Budget End
2011-04-30
Support Year
36
Fiscal Year
2010
Total Cost
$346,125
Indirect Cost
Name
University of California Davis
Department
Type
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Crowley, Candace M; Fontaine, Justin H; Gerriets, Joan E et al. (2017) Early life allergen and air pollutant exposures alter longitudinal blood immune profiles in infant rhesus monkeys. Toxicol Appl Pharmacol 328:60-69
Hsia, Connie C W; Hyde, Dallas M; Weibel, Ewald R (2016) Lung Structure and the Intrinsic Challenges of Gas Exchange. Compr Physiol 6:827-95
Herring, Matt J; Avdalovic, Mark V; Lasley, Bill et al. (2016) Elderly Female Rhesus Macaques Preserve Lung Alveoli With Estrogen/Progesterone Therapy. Anat Rec (Hoboken) 299:973-8
Lynn, Therese M; Molloy, Emer L; Masterson, Joanne C et al. (2016) SMAD Signaling in the Airways of Healthy Rhesus Macaques versus Rhesus Macaques with Asthma Highlights a Relationship Between Inflammation and Bone Morphogenetic Proteins. Am J Respir Cell Mol Biol 54:562-73
Herring, M J; Putney, L F; St George, J A et al. (2015) Early life exposure to allergen and ozone results in altered development in adolescent rhesus macaque lungs. Toxicol Appl Pharmacol 283:35-41
Van Winkle, Laura S; Bein, Keith; Anderson, Donald et al. (2015) Biological dose response to PM2.5: effect of particle extraction method on platelet and lung responses. Toxicol Sci 143:349-59
Madl, Amy K; Plummer, Laurel E; Carosino, Christopher et al. (2014) Nanoparticles, lung injury, and the role of oxidant stress. Annu Rev Physiol 76:447-65
Herring, Matt J; Putney, Lei F; Wyatt, Gregory et al. (2014) Growth of alveoli during postnatal development in humans based on stereological estimation. Am J Physiol Lung Cell Mol Physiol 307:L338-44
Moore, Brian D; Hyde, Dallas M; Miller, Lisa A et al. (2014) Persistence of serotonergic enhancement of airway response in a model of childhood asthma. Am J Respir Cell Mol Biol 51:77-85
Murphy, Shannon R; Oslund, Karen L; Hyde, Dallas M et al. (2014) Ozone-induced airway epithelial cell death, the neurokinin-1 receptor pathway, and the postnatal developing lung. Am J Physiol Lung Cell Mol Physiol 307:L471-81

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