Peroxynitrite Modulates Release of Inflammatory Mediators from Guinea Pig Lung Mast Cells Activated by Antigen-Antibody Reaction

• Published in: International Archives of Allergy and Immunology 2005-06, Vol.137 (2), p.104-114
• Main Authors: Kim, Ji Young, Lee, Kwang Hoon, Lee, Bong Ki, Ro, Jai Youl
• Format: Article
• Language: English
• Subjects: Animals; Antigen-Antibody Reactions; Antigens; Antioxidants - pharmacology; Biological and medical sciences; Calcium - metabolism; Cells; Female; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Guinea Pigs; Histamine Release; Immunoglobulins; Immunology; Immunopathology; Leukotrienes - metabolism; Lung - cytology; Lung - immunology; Lungs; Mast Cells - immunology; Medical sciences; Nitric Oxide - metabolism; Original Paper; Peroxynitrous Acid - physiology; Phospholipases A - metabolism; Reactive Oxygen Species - metabolism; Rodents; Tyrosine - analysis
• ISSN: 1018-2438; 1423-0097; 1365-2567
• DOI: 10.1159/000085465

Background: Peroxynitrite (ONOO – ), the product of the reaction between the superoxide anion (·O 2 – ) and nitric oxide (NO), is produced during inflammatory disease and may be a major cytotoxic agent. No reports are available as to whether ONOO – generates or modulates inflammatory mediator release from activated guinea pig lung mast cells. In this study, we explored the modulatory role of intracellular ONOO – on inflammatory mediator release (histamine and leukotrienes) from activated mast cells. Methods: Guinea pig lung mast cells were purified by the enzyme digestion, and by using the rough and discontinuous Percoll density gradients. Mast cells were sensitized with IgG1 (anti-ovalbumin) antibody and challenged with ovalbumin (OVA). The intracellular ROS formation was determined by following the oxidative production of 2′, 7′-dichlorofluorescein diacetate (DCFH-DA), dihydrorhodamine 123 (DHR), and anti-nitrotyrosine antibody immunofluorescence. Histamine was assayed using a fluorometric analyzer, leukotrienes by radioimmunoassay, intracellular Ca 2+ levels by confocal scanning microscopy, and PLA 2 activity using prelabeling of [ 3 H]arachidonic acid. Results: ROS detected by DCFH-DA weakly increased in mast cells activated with OVA (1.0 g/ml), and the ROS so generated was inhibited by ebselen (50 µM). However, the ROS detected by DHR increased 3-fold under the same conditions. Peroxynitrite scavengers sL-MT, DMTU, and inhibitor FeTPPS inhibited ROS formation but the NADPH oxidase inhibitor diphenyleneiodonium (DPI) only partially inhibited this formation. Dimethyl thiourea (DMTU) and seleno-L-methionine (sL-MT) inhibited the tyrosine nitration of cytosolic proteins, the release of histamine and leukotrienes, Ca 2+ influx, and the PLA 2 activity evoked by mast cell activation. Conclusion: The data obtained suggests that the ROS generated by the antigen/antibody reaction activated mast cells is ONOO – , and that this modulates the release of inflammatory mediators via Ca 2+ -dependent PLA 2 activity.