Cysteinyl leukotrienes acting via granule membrane-expressed receptors elicit secretion from within cell-free human eosinophil granules

• Published in: Journal of allergy and clinical immunology 2010-02, Vol.125 (2), p.477-482
• Main Authors: Neves, Josiane S., PhD, Radke, Amy L., BS, Weller, Peter F., MD
• Format: Article
• Language: English
• Subjects: Acetates - pharmacology; allergy; Allergy and Immunology; asthma; Biological and medical sciences; Blotting, Western; Cell Separation; Cell-Free System; Chemokines; Chronic obstructive pulmonary disease, asthma; Cysteine - metabolism; Cysteine - pharmacology; cysteinyl leukotriene; eosinophil; Eosinophil Cationic Protein - drug effects; Eosinophil Cationic Protein - secretion; Eosinophils - ultrastructure; Flow Cytometry; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Granules; Humans; Immunopathology; Leukotriene Antagonists - pharmacology; Leukotrienes - metabolism; Leukotrienes - pharmacology; Ligands; Medical sciences; Membranes; montelukast; Peptides; Plasma; Pneumology; Polyclonal antibodies; Proteins; Quinolines - pharmacology; Receptors, Leukotriene - metabolism; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis; Secretory Vesicles - drug effects; Secretory Vesicles - secretion
• ISSN: 0091-6749; 1097-6825
• DOI: 10.1016/j.jaci.2009.11.029

Background Cysteinyl leukotrienes (cysLTs) are recognized to act via receptors (cysLTRs) expressed on cell surface plasma membranes. Agents that block cysLT1 receptor (cysLT1 R) are therapeutics for allergic disorders. Eosinophils contain multiple preformed proteins stored within their intracellular granules. Cell-free eosinophil granules are present extracellularly as intact membrane-bound organelles in sites associated with eosinophil infiltration, including asthma, rhinitis, and urticaria, but have unknown functional capabilities. Objective We evaluated the expression of cysLTRs on eosinophil granule membranes and their functional roles in eliciting protein secretion from within eosinophil granules. Methods We studied secretory responses of human eosinophil granules isolated by subcellular fractionation. Granules were stimulated with cysLTs, and eosinophil cationic protein and cytokines were measured in the supernatants. Receptor expression on granule membranes and eosinophils was evaluated by flow cytometry and Western blot. Results We report that receptors for cysLTs, cysLT1 R, cysLT2 receptor, and the purinergic P2Y12 receptor, are expressed on eosinophil granule membranes. Leukotriene (LT) C4 and extracellularly generated LTD4 and LTE4 stimulated isolated eosinophil granules to secrete eosinophil cationic protein. MRS 2395, a P2Y12 receptor antagonist, inhibited cysLT-induced eosinophil cationic protein release. Montelukast, likely not solely as an inhibitor of cysLT1 R, inhibited eosinophil cationic protein release elicited by LTC4 and LTD4 as well as by LTE4. Conclusion These studies identify previously unrecognized sites of localization, the membranes of intracellular eosinophil granule organelles, and function for cysLT-responsive receptors that mediate cysteinyl leukotriene-stimulated secretion from within eosinophil granules, including those present extracellularly.