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Analysis of FcγRIIA Cytoplasmic Tail Requirements in Signaling for Serotonin Secretion: Evidence for an ITAM‐Dependent, PI3K‐Dependent Pathway
Author(s) -
Daniels A. B.,
Worth R. G.,
Dickstein R. J.,
Dickstein J. S.,
KimHan T.H.,
Kim M.K.,
Schreiber A. D.
Publication year - 2010
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1111/j.1365-3083.2010.02369.x
Subject(s) - biology , tyrosine , signal transduction , microbiology and biotechnology , secretion , serotonin , biochemistry , receptor
The human Fc receptor, FcγRIIA, is known to mediate phagocytosis and endocytosis, yet the greatest numbers of these receptors are expressed on the surface of non‐phagocytic platelets, where they are involved in serotonin secretion. FcγRIIA harbours three tyrosine (Y) residues within its cytoplasmic domain. Y1 is upstream of both Y2 and Y3, which are contained within an immunoreceptor tyrosine‐based activation motif (ITAM), required for many signaling events. We have demonstrated that the two ITAM tyrosines are required for phagocytic signaling and that mutation of a single ITAM tyrosine decreases but does not abolish phagocytic signaling. Furthermore, we have identified that the YMTL motif is required for endocytosis. These observations suggest that FcγRIIA utilizes different sequences for various signaling events. Therefore, we investigated the sequence requirements for another important FcγRIIA‐mediated signaling event, serotonin secretion, using Rat Basophilic Leukemia (RBL‐2H3) cells transfected with wildtype (WT) FcγRIIA or mutant FcγRIIA. Stimulation of cells expressing WT FcγRIIA induced release of serotonin at a level 7‐fold greater than that in nonstimulated WT FcγRIIA‐transfected cells or nontransfected RBL cells. Mutation of either ITAM tyrosine (Y2 or Y3) to phenylalanine was sufficient to abolish serotonin secretion. Further, while inhibition of Syk with piceatannol blocked phagocytosis as expected, it did not inhibit serotonin secretion. Additionally, inhibition of phosphoinositol‐3‐kinase (PI3K) with wortmannin only had a partial effect on serotonin signaling, despite the fact that the concentrations used completely abolished phagocytic signaling. These data suggest that the requirements for serotonin secretion differ from those for phagocytosis mediated by FcγRIIA.