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Eosinophil granules function extracellularly as receptor-mediated secretory organelles

Authors :
Peter F. Weller
Redwan Moqbel
Sandra A.C. Perez
Ionita Ghiran
Salahaddin Mahmudi-Azer
Lauren E. Reynolds
Josiane S. Neves
Lisa A. Spencer
Ann M. Dvorak
Rossana C. N. Melo
S.O. Odemuyiwa
Source :
Proceedings of the National Academy of Sciences. 105:18478-18483
Publication Year :
2008
Publisher :
Proceedings of the National Academy of Sciences, 2008.

Abstract

Intracellular granules in several types of leukocytes contain preformed proteins whose secretions contribute to immune and inflammatory functions of leukocytes, including eosinophils, cells notably associated with asthma, allergic inflammation, and helminthic infections. Cytokines and chemokines typically elicit extracellular secretion of granule proteins by engaging receptors expressed externally on the plasma membranes of cells, including eosinophils. Eosinophil granules, in addition to being intracellular organelles, are found as intact membrane-bound structures extracellularly in tissue sites of eosinophil-associated diseases. Neither the secretory capacities of cell-free eosinophil granules nor the presence of functional cytokine and chemokine receptors on membranes of leukocyte granules have been recognized. Here, we show that granules of human eosinophils express membrane receptors for a cytokine, IFN-γ, and G protein–coupled membrane receptors for a chemokine, eotaxin, and that these receptors function by activating signal-transducing pathways within granules to elicit secretion from within granules. Capacities of intracellular granule organelles to function autonomously outside of eosinophils as independent, ligand-responsive, secretion-competent structures constitute a novel postcytolytic mechanism for regulated secretion of eosinophil granule proteins that may contribute to eosinophil-mediated inflammation and immunomodulation.

Details

ISSN :
10916490 and 00278424
Volume :
105
Database :
OpenAIRE
Journal :
Proceedings of the National Academy of Sciences
Accession number :
edsair.doi.dedup.....7e77076f7b0cc81448e472956a99d5be
Full Text :
https://doi.org/10.1073/pnas.0804547105