The Southern California Children's Environmental Health Center (SC-CEHC) is studying the role of ubiquitous ambient near-roadway air pollution (NRAP) on childhood obesity and associated risk for type 2 diabetes. A multidisciplinary team in an integrated program of population-based, clinical and experimental research is capitalizing on resources of the Southern California Children's Health Study to examine the association of lifetime cumulative NRAP exposure to adipose tissue inflammation and related metabolic outcomes including fat distribution, glucose homeostasis, lipid profile, and systemic inflammation using cutting edge exposure assessment, imaging and metabolic phenotyping in overweight/obese young adults from the cohort. The role of immune modulation of adipose tissue inflammation is increasingly recognized as central to the development of diabetes and metabolic disease in obese people; therefore, a key question for the Center is the impact of NRAP on the immune cell profile of adipose tissue. However, this is a rapidly evolving field, and recent studies from our research group and others indicate that additional members of the innate and adaptive arms of the immune system, in particular T effector (Teff) and T regulatory (Treg) cells, modulate the pathogenesis of adipose tissue inflammation, insulin resistance and diabetes. In addition, one recent report found decreased expression of Teff cells in peripheral blood of children exposed to particulate air pollution. In addition to our original aims in the Center to examine macrophage polarity in adipose tissue, we now propose to measure Teff and Treg cell number in blood and in deep (subfascial) subcutaneous adipose tissue (dSAT) in 60 overweight/obese cohort participants. These subjects will be a sub-group of 200 participants who have been informatively selected from the cohort based on lifetime NRAP exposure and who are undergoing detailed metabolic evaluation in the Center. We hypothesize that lifetime NRAP exposure will increase pro-inflammatory Teff cell count and decrease anti-inflammatory Treg cells in blood and adipose tissue, and that these cells will be associated with inflammation and insulin resistance in dSAT. The results will be used to refine an innovative latent variable hierarchical statistical model integrating information across projects to examine the influence of immune phenotype on the effects of NRAP on metabolic risk, using information from the entire cohort of almost 5000 children. The SC-CEHC provides an opportunity to address key gaps in our understanding of the immune mechanisms underlying associations of air pollution with risk factors for type 2 diabetes and to create a resource for future evaluation of expression pathways, if support can be provided in time to characterize fresh tissue in subjects undergoing recruitment on a tight timeframe.

Public Health Relevance

This time-sensitive application building on the infrastructure of the Southern California Children's Environmental Health Center proposes to examine the role of T effector and T regulatory cells in the impact of near-roadway air pollution on adipose tissue inflammatory profile. The study has the potential to fill critical gaps in our understanding of the reasons obesity increases the risk of diabetes and to identify mechanisms that might be targets for prevention efforts.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21ES024707-02
Application #
8887338
Study Section
Special Emphasis Panel (ZES1)
Program Officer
Joubert, Bonnie
Project Start
2014-07-10
Project End
2017-06-30
Budget Start
2015-07-01
Budget End
2017-06-30
Support Year
2
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of Southern California
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90032
Hsieh, S; Leaderer, B P; Feldstein, A E et al. (2018) Traffic-related air pollution associations with cytokeratin-18, a marker of hepatocellular apoptosis, in an overweight and obese paediatric population. Pediatr Obes 13:342-347
Ghosh, R; Gauderman, W J; Minor, H et al. (2018) Air pollution, weight loss and metabolic benefits of bariatric surgery: a potential model for study of metabolic effects of environmental exposures. Pediatr Obes 13:312-320
Wolff, Mary S; Buckley, Jessie P; Engel, Stephanie M et al. (2017) Emerging exposures of developmental toxicants. Curr Opin Pediatr 29:218-224
Rigas, Diamanda; Lewis, Gavin; Aron, Jennifer L et al. (2017) Type 2 innate lymphoid cell suppression by regulatory T cells attenuates airway hyperreactivity and requires inducible T-cell costimulator-inducible T-cell costimulator ligand interaction. J Allergy Clin Immunol 139:1468-1477.e2
Maazi, Hadi; Akbari, Omid (2017) Type two innate lymphoid cells: the Janus cells in health and disease. Immunol Rev 278:192-206
Suzuki, Yuzo; Maazi, Hadi; Sankaranarayanan, Ishwarya et al. (2016) Lack of autophagy induces steroid-resistant airway inflammation. J Allergy Clin Immunol 137:1382-1389.e9
McConnell, R; Gilliland, F D; Goran, M et al. (2016) Does near-roadway air pollution contribute to childhood obesity? Pediatr Obes 11:1-3
McConnell, Rob; Shen, Ernest; Gilliland, Frank D et al. (2015) A longitudinal cohort study of body mass index and childhood exposure to secondhand tobacco smoke and air pollution: the Southern California Children's Health Study. Environ Health Perspect 123:360-6
Maazi, Hadi; Patel, Nisheel; Sankaranarayanan, Ishwarya et al. (2015) ICOS:ICOS-ligand interaction is required for type 2 innate lymphoid cell function, homeostasis, and induction of airway hyperreactivity. Immunity 42:538-51
Jerrett, Michael; McConnell, Rob; Wolch, Jennifer et al. (2014) Traffic-related air pollution and obesity formation in children: a longitudinal, multilevel analysis. Environ Health 13:49