The CD200 Receptor Is a Novel and Potent Regulator of Murine and Human Mast Cell Function
Author(s) -
Holly Cherwinski,
Craig A. Murphy,
Barbara Joyce,
Mike Bigler,
Yaoli Song,
Sandra Zurawski,
Mehrdad Moshrefi,
Daniel M. Gorman,
Kathy L. Miller,
Shuli Zhang,
Jonathan D. Sedgwick,
Joseph H. Phillips
Publication year - 2005
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.174.3.1348
Subject(s) - mast cell , microbiology and biotechnology , degranulation , receptor , in vivo , biology , cytokine , immune system , immunology , chemistry , biochemistry
CD200R is a member of the Ig supergene family that is primarily expressed on myeloid cells. Recent in vivo studies have suggested that CD200R is an inhibitory receptor capable of regulating the activation threshold of inflammatory immune responses. Here we provide definitive evidence that CD200R is expressed on mouse and human mast cells and that engagement of CD200R by agonist Abs or ligand results in a potent inhibition of mast cell degranulation and cytokine secretion responses. CD200R-mediated inhibition of FcepsilonRI activation was observed both in vitro and in vivo and did not require the coligation of CD200R to FcepsilonRI. Unlike the majority of myeloid inhibitory receptors, CD200R does not contain a phosphatase recruiting inhibitory motif (ITIM); therefore, we conclude that CD200R represents a novel and potent inhibitory receptor that can be targeted in vivo to regulate mast cell-dependent pathologies.
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