Asthma is a common, non-communicable disorder characterized by airway inflammation and airflow obstruction. In addition to environmental triggers and genetic susceptibility, obesity has emerged as a major risk factor for asthma, suggesting that these two chronic diseases may share common mechanisms. In the past few decades, it has become clear that the action of fatty acid binding protein (FABP) aP2 significantly contributes to metabolic diseases associated with obesity, with complementary data produced in both experimental models and in humans. In recent experiments presented here, we detected aP2 in the bronchial epithelium and bronchoalveolar lavage fluid in an allergen-induced model of asthma in mice, and determined that aP2-deficient mice were significantly protected from developing disease in this model. Our overarching hypothesis is that aP2 plays an important role in the development of inflammatory responses and airway hyper-responsiveness in asthma, and in the link between obesity and asthma. The studies described in the current proposal will test this hypothesis by identifying the cellular source and mechanisms of aP2 action (Aim1), determining the impact of circulating aP2 in asthma (Aim2), and finally, by evaluating the efficacy of a small molecule aP2 inhibitor and a neutralizing antibody as asthma therapy (Aim3). Successful completion of the proposed project will not only expand our knowledge related to the pathophysiology of asthma development and the relationship between asthma and obesity, but also may reveal novel mechanisms and new therapeutic approaches against this common disease.

Public Health Relevance

Recent evidence demonstrates that obesity is a major risk factor for the development of asthma. The proposed research will reveal the identity and mechanisms of the molecular players that underlie the connection between these two epidemics. This work will result in a better understanding of airway inflammation in obesity and could lead to the development of new strategies to prevent and manage asthma, reflecting the stated goal of NIH- supported asthma research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI116901-03
Application #
9222708
Study Section
Lung Cellular, Molecular, and Immunobiology Study Section (LCMI)
Program Officer
Dong, Gang
Project Start
2015-03-15
Project End
2019-02-28
Budget Start
2017-03-01
Budget End
2018-02-28
Support Year
3
Fiscal Year
2017
Total Cost
$403,750
Indirect Cost
$153,750
Name
Harvard University
Department
Genetics
Type
Schools of Public Health
DUNS #
149617367
City
Boston
State
MA
Country
United States
Zip Code
02115
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Charles, Khanichi N; Li, Min-Dian; Engin, Feyza et al. (2017) Uncoupling of Metabolic Health from Longevity through Genetic Alteration of Adipose Tissue Lipid-Binding Proteins. Cell Rep 21:393-402
Hotamisligil, Gökhan S (2017) Foundations of Immunometabolism and Implications for Metabolic Health and Disease. Immunity 47:406-420
Ertunc, Meric Erikci; Hotamisligil, Gökhan S (2016) Lipid signaling and lipotoxicity in metaflammation: indications for metabolic disease pathogenesis and treatment. J Lipid Res 57:2099-2114
Yilmaz, Mustafa; Claiborn, Kathryn C; Hotamisligil, Gökhan S (2016) De Novo Lipogenesis Products and Endogenous Lipokines. Diabetes 65:1800-7
Arruda, Ana Paula; Hotamisligil, Gökhan S (2015) Calcium Homeostasis and Organelle Function in the Pathogenesis of Obesity and Diabetes. Cell Metab 22:381-97