Journal
MICROBIAL PATHOGENESIS
Volume 44, Issue 4, Pages 286-292Publisher
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.micpath.2007.10.008
Keywords
Mast cells; Mycoplasma pneumoniae; Cytokines; Fc receptors; Asthma
Categories
Funding
- NHLBI [P01 HL073907-04]
- NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [P01HL073907] Funding Source: NIH RePORTER
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We have previously described the activation of RBL-2H3 mast cells for IL-4 production by Mycoplasma pneumoniae but the mechanism remains unclear. M. pneumoniae binds eukaryotic cells primarily through sialoglycoproteins on the target cell surface. This study was undertaken to determine whether the sialated Fc epsilon RI alpha chain on RBL cells is important for M. pneumoniae-induced IL-4 production. We found that IgE-mediated IL-4 release by a series of RBL sublines correlated with the release induced by M. pneumoniae. Further, aggregation of Fc gamma RII (CD32) in RBL cells using a monoclonal antibody inhibited both IgE-mediated and mycoplasma-induced IL-4 production, providing further evidence for an Fc receptor-mediated mechanism of activation. To examine the role of Fc epsilon RI in mycoplasma-induced IL-4 release, we created stably transfected RBL sublines using a vector expressing a short hairpin sequence designed to inhibit message for the Fc epsilon RI alpha chain. IgE-induced IL-4 production by the transfected sublines was reduced in similar proportion to the degree of message Suppression. M. pneumoniae-induced IL-4 production in the four transfected sublines was completely blocked in contrast to results With the controls or parent RBL cells. We conclude that the heavily glycosylated Fc epsilon RI alpha chain is required for activation of mast cells for IL-4 production by M. pneumoniae. (C) 2007 Elsevier Ltd. All rights reserved.
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