Pulmonary granuloma formation is a key feature of sarcoidosis, a chronic disease of unknown etiology. Sarcoidosis has been linked to environmental risk factors (wood-burning stoves, fireplaces and firefighting) that favor carbon nanotube formation. We have shown that lungs instilled with multiwall carbon nanotubes (MWCNT) produce chronic inflammation and granuloma formation resembling sarcoidosis. Sarcoidosis alveolar macrophages exhibit elevated pro-inflammatory cytokines such as CCL5 and IFN-?, but are deficient in PPAR ?, a lipid regulator that regulates the ABC transporters A1/G1 and dampens inflammation. This phenotype appears in macrophages from MWCNT-instilled mice. In macrophage-specific PPAR ?-KO mice, inflammatory mediators and granulomatous disease are exacerbated, suggesting that PPAR? is protective. Preliminary data indicate elevated microRNA (miR)-33 in macrophages and granulomatous tissues from both sarcoid patients and MWCNT-instilled mice. The role of miR-33 in the lung is unknown, but elsewhere miR-33 is shown to increase inflammation and repress ABCA1 and ABCG1 lipid transporters (which have anti- inflammatory properties). Strikingly, both transporters are depressed in macrophages from sarcoid patients and MWCNT-instilled mice. Further, in vitro miR-33 overexpression in wild type alveolar macrophages decreases ABCA1 and ABCG1 but not PPAR?. These results suggest that two pathways may dysregulate transporters in granulomatous disease - one associated with intrinsic PPAR? status and the other via environmentally triggered miR-33. We hypothesize that granuloma-protective pathways of PPAR? are mediated by anti-inflammatory actions of ABCA1 and/or ABCG1.
Aim 1 will determine functional significance of lipid transporters in granulomatous disease. MWCNT will be instilled in macrophage-specific KO models of: PPAR?, ABCA1, ABCG1, and ABCA1/ABCG1 (double KO) plus wild-type mice. Sixty days later, untreated, sham-(vehicle) treated, or MWCNT-instilled mice will be examined for granuloma size/frequency, and alveolar macrophage expression of ABCA1, ABCG1, miR-33, CCL5, IFN?, PPAR?, and intracellular cholesterol.
Aim 2 will explore the role of miR-33 as a mediator in granulomatous disease and alveolar macrophage expression of ABCA1 and ABCG1. MWCNT-instilled wild-type and macrophage-specific PPAR? KO mice will receive lenti-control, lenti-miR-33, or lenti-miR-33 antagomir. Granuloma size/frequency and alveolar macrophage markers will be evaluated.
Sub aims will examine miR-33 and lipid transporters in murine and healthy human alveolar macrophages cultured with MWCNT.
Aim 3 will determine whether ABCA1, ABCG1, and miR-33 are intrinsically dysregulated in sarcoid alveolar macrophages compared to healthy controls.
Sub aims will examine effects of lenti-ABCA1, lenti-ABCG1, or lenti-miR-33 antagomir on alveolar macrophages. Our murine MWCNT granuloma model provides a unique opportunity for defining mechanisms and components perpetuating chronicity in environmental lung disease.

Public Health Relevance

The current application addresses the environmental health issue of possible carbon nanotube involvement in human granulomatous lung disease. In particular, sarcoidosis, a proto-typical granulomatous lung disease of unknown cause, has been linked by epidemiologic studies to environmental conditions favoring carbon nanotube formation in ambient air. Sarcoidosis is also endemic in the coastal areas of the Carolinas and is 4 to 17 times more common in African- Americans than in Caucasians. This project seeks to utilize a novel murine granuloma model in order to investigate the impact of carbon nanotubes on granuloma formation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
1R01ES025191-01A1
Application #
9110469
Study Section
Nanotechnology Study Section (NANO)
Program Officer
Nadadur, Srikanth
Project Start
2016-07-01
Project End
2021-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
1
Fiscal Year
2016
Total Cost
$314,824
Indirect Cost
$96,893
Name
East Carolina University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
607579018
City
Greenville
State
NC
Country
United States
Zip Code
27858