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- W1636369673 abstract "Abstract The correct mobilization of cytoplasmic granules is essential for the proper functioning of human neutrophils in host defense and inflammation. In this study, we have found that human peripheral blood neutrophils expressed high levels of Rab27a, whereas Rab27b expression was much lower. This indicates that Rab27a is the predominant Rab27 isoform present in human neutrophils. Rab27a was up-regulated during neutrophil differentiation of HL-60 cells. Subcellular fractionation and immunoelectron microscopy studies of resting human neutrophils showed that Rab27a was mainly located in the membranes of specific and gelatinase-enriched tertiary granules, with a minor localization in azurophil granules. Rab27a was largely absent from CD35-enriched secretory vesicles. Tertiary and specific granule-located Rab27a population was translocated to the cell surface upon neutrophil activation with PMA that induced exocytosis of both tertiary and specific granules. Specific Abs against Rab27a inhibited Ca2+ and GTP-γ-S activation and PMA-induced exocytosis of CD66b-enriched tertiary and specific granules in electropermeabilized neutrophils, whereas secretion of CD63-enriched azurophil granules was scarcely affected. Human neutrophils lacked or expressed low levels of most Slp/Slac2 proteins, putative Rab27 effectors, suggesting that additional proteins should act as Rab27a effectors in human neutrophils. Our data indicate that Rab27a is a major component of the exocytic machinery of human neutrophils, modulating the secretion of tertiary and specific granules that are readily mobilized upon neutrophil activation." @default.
- W1636369673 created "2016-06-24" @default.
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- W1636369673 creator A5063187405 @default.
- W1636369673 date "2008-09-15" @default.
- W1636369673 modified "2023-10-16" @default.
- W1636369673 title "Rab27a Regulates Exocytosis of Tertiary and Specific Granules in Human Neutrophils" @default.
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- W1636369673 doi "https://doi.org/10.4049/jimmunol.181.6.3793" @default.
- W1636369673 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18768832" @default.
- W1636369673 hasPublicationYear "2008" @default.
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