The Effects of air-borne particulate matters on the Alveolar Macrophages for the iNOS Expression and Nitric Oxide with Nitrotyrosilated-proteins Formation.
10.4046/trd.2006.60.4.426
- Author:
Feng Ji CUI
1
;
Tian Zhu LI
;
Soo Jin LEE
;
Se Jong PARK
;
Young LIM
;
Kyung A KIM
;
Byung Joon CHANG
;
Jong Hwan LEE
;
Myoung Heon LEE
;
Nong Hoon CHOE
Author Information
1. College of Veterinary Medicine, Konkuk university, Seoul, Korea. nojamaji@hanmail.net
- Publication Type:Original Article
- Keywords:
Particulate matter (PM);
Rat lung alveolar macrophages;
Nitric oxide (NO);
Inducible nitric oxide synthase (iNOS);
Nitrotyrosilated-protein
- MeSH:
Animals;
Asthma;
Blotting, Western;
Bronchitis, Chronic;
Bronchoalveolar Lavage;
Cells, Cultured;
Lung Diseases;
Lung Injury;
Macrophages, Alveolar*;
Nitric Oxide Synthase Type II;
Nitric Oxide*;
Rats
- From:Tuberculosis and Respiratory Diseases
2006;60(4):426-436
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Particulate matters (PM) when inhaled is known to induce pulmonary diseases including asthma and chronic bronchitis when inhaled. Despite the epidemiological proofevidence, the pathogenesis of PM-related pulmonary diseases is unclearremain poorly understood. METHODS: Primary alveolar macrophages were harvested from the SPF and inflammatory rats by bronchioalveolar lavage (BAL). The cultured primary alveolar macrophages were treated with the medium only, PM only (5~40 microgram/cm2), LPS (5ng/ml) only, and PM with LPS for 24 and 48 hours. The level of secreted nitric oxide (NO) was assayed from the cultured medium by using the Griess reaction. The cultured cells were utilized for the western blotting against the inducible nitric oxide synthase (iNOS) proteins. Immunocyto- chemical staining against the iNOS and NT-proteins were performed in cells that cultured in the Lab-Tek(R) chamber slide after treatments. RESULTS: The PM that utilizein this experiments induced NO formation with iNOS expression in the cultured SPF and inflammatory rats alveolar macrophages, by itself. When the cells were co-treated with PM and LPS, there was a statistically significant synergistic effect on NO formation and iNOS expression over the LPS effect. The cells from the sham control showed minimal immunoreactivity for the NT-proteins. Significantly higher quantities of NT-proteins were detected in the PM and PM with LPS co-treated cells than from the sham control. CONCLUSION: Increased iNOS expression and NO formation with increased NT-proteins formation might be involved in the pathogenesis of PM-induced lung injury.
