1. Leukotrienes C4 and D4 sensitize human neutrophils for hyperreactivity to chemoattractants.
- Author
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Theron AJ, Gravett CM, Steel HC, Tintinger GR, Feldman C, and Anderson R
- Subjects
- Acetates metabolism, Adult, Cyclopropanes, Fluorescent Dyes metabolism, Fura-2 analogs & derivatives, Fura-2 metabolism, Humans, Leukotriene Antagonists metabolism, Leukotriene C4 immunology, Leukotriene D4 immunology, Matrix Metalloproteinase 8 metabolism, N-Formylmethionine Leucyl-Phenylalanine metabolism, Neutrophils cytology, Pancreatic Elastase metabolism, Quinolines metabolism, Sulfides, Superoxides metabolism, Chemotactic Factors immunology, Inflammation immunology, Leukotriene C4 pharmacology, Leukotriene D4 pharmacology, Neutrophils drug effects, Neutrophils immunology
- Abstract
Objective and Design: To investigate the sensitizing effects of the cysteinyl leukotrienes (CysLTs) C(4) and D(4) on the proinflammatory responses of chemoattractant-activated human neutrophils in vitro., Materials: Neutrophils were isolated from venous blood taken from healthy, adult, human volunteers., Treatment: Cells were exposed to LTC(4) and LTD(4) (50-300 nM) prior to activation with 1 microM of N-formyl-L-methionyl- L-leucyl-L-phenylalanine (fMLF)., Methods: A fura-2/AM-based spectrofluorimetric procedure, lucigenin-enhanced chemiluminescence (LECL), a colourimetric method and an ELISA procedure, were used to measure Ca(2+) mobilization, superoxide production, elastase and MMP-8 release respectively following activation of LTC(4)/ D(4)-primed neutrophils with fMLF. Superoxide generation was also measured in the presence and absence of the CysLT receptor 1 antagonist, montelukast (100 nM)., Results: Exposure of neutrophils to either LTC(4) or LTD(4) alone had modest effects on Ca(2+) mobilization, while superoxide generation and elastase release were unaffected. However, relative to the responses of neutrophils activated with fMLF in the absence of the CysLTs, pre-treatment of the cells with either LTC(4)or LTD(4) resulted in significant, augmentation of fMLF-activated elastase and MMP-8 release and superoxide generation, which was attenuated by montelukast., Conclusion: These previously undocumented sensitizing interactions of LTs C(4) and D(4) with neutrophils may contribute to the activation of these cells in acute and chronic inflammation of both atopic and non-atopic aetiology, while identifying a role for montelukast in regulating neutrophil reactivity.
- Published
- 2009
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