Abstract
Background: Exocytosis is an integral event during IFN-γ-induced piecemeal degranulation in eosinophils. In many tissues soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs), including vesicle-associated membrane protein (VAMP), act as specific intracellular receptors to allow granule fusion with the membrane during degranulation. However, the mechanisms underlying eosinophil piecemeal degranulation induced by IFN-γ are not well understood. Objective: We sought to assess whether eosinophils express the vesicular SNARE protein VAMP-2 and to determine the involvement of VAMP-2 in IFN-γ-induced piecemeal degranulation. Methods: Human peripheral blood eosinophils (≥97%) from atopic subjects were subjected to RT-PCR and sequence analysis with specific primers for VAMP-2 mRNA. Western blotting and flow cytometric analysis were carried out to confirm the identity of VAMP-2 and its susceptibility to cleavage by tetanus toxin. Confocal laser scanning microscopy imaging was conducted on double-labeled cytospin preparations of eosinophils at 0, 5, 10, 30, and 60 minutes and 16 hours of IFN-γ (500 U/mL) stimulation. Results: Eosinophils expressed VAMP-2 mRNA (n = 4 donors), which exhibited 100% homology with human VAMP-2 cDNA on sequencing. Eosinophils were also found to express tetanus toxin-sensitive VAMP-2 protein. RANTES and VAMP-2 immunofluorescence were observed to colocalize to similar intracellular structures by means of confocal imaging. IFN-γ induced a rapid translocation of VAMP-2+ organelles toward the cell membrane in correlation with RANTES. Conclusions: These findings suggest that exocytosis in human eosinophils is regulated by SNAREs, with a specific role indicated for VAMP-2 in piecemeal degranulation. © 2001 Elsevier Science Ltd. All rights reserved.
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Lacy, P., Logan, M. R., Bablitz, B., & Moqbel, R. (2001). Fusion protein vesicle-associated membrane protein 2 is implicated in IFN-γ-induced piecemeal degranulation in human eosinophils from atopic individuals. Journal of Allergy and Clinical Immunology, 107(4), 671–678. https://doi.org/10.1067/mai.2001.113562
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