Lung proteins are obvious targets for reaction with inhaled air pollutants and the project focuses on the molecular mechanisms by which inhaled oxidants may damage proteins vital to the normal structure and function of the lung. In vitro O3 and NO2 exposures of human alpha-1proteinase inhibitor (alpha1-PI) and bronchial leukocyte proteinase inhibitor (BLPI), which protect the lung from emphysema by inhibiting protein degrading enzymes, will be performed to determine the susceptibility of these inhibitors to pollutant oxidants. Exposures of inhibitors and unsaturated hydrocarbons, as well as membrane entrapped inhibitors, will determine whether the autoxidation of unsaturated fatty acids contributes to inhibitor inactivation; thus diminishing the lung's defenses. Elastin is the major structural protein of the lung alveoli and preliminary data show that O3 and NO2 directly alter the structure of elastin and make it more susceptible to proteolysis. The mechanism(s) of this reaction(s) will be investigated using techniques such as amino acid analysis, HPLC peptide mapping and electrophoresis. Tryptase is the principal granular protein of human mast cells. Antibodies to tryptase, that cross-react with a similar protein in cultured mouse mastocytoma cells, will be used to study the effects of O3 and NO2 on the degranulation of the mast cells, to test the hypothesis that oxidant induced degranulation of mast cells accounts for many of the acute physiological effects of oxidants on the lung. Increased levels of mast cell tryptase have been observed in nasal and bronchoalveolar lavage fluids from O3-exposed humans. Additional studies are planned to characterize this response with regard to O3 and NO2, and to provide in vivo data for interpretation of in vitro results with cultured mast cells. Knowledge will be gained on the molecular and cellular reactions of O3 and NO2, which could lead to better markers of oxidant exposure and eventually to methods of intervention or protection from the adverse effects of O3 and NO2.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES004999-03
Application #
3253212
Study Section
Toxicology Subcommittee 2 (TOX)
Project Start
1990-07-01
Project End
1994-03-31
Budget Start
1992-07-01
Budget End
1994-03-31
Support Year
3
Fiscal Year
1992
Total Cost
Indirect Cost
Name
East Tennessee State University
Department
Type
Schools of Medicine
DUNS #
City
Johnson City
State
TN
Country
United States
Zip Code
37614