Mast cell–expressed orphan receptor CCRL2 binds chemerin and is required for optimal induction of IgE-mediated passive cutaneous anaphylaxis

Brian A. Zabel(VA Palo Alto Health Care System), Susumu Nakae(Stanford University), Luis Zúñiga(VA Palo Alto Health Care System), Jiyun Kim(VA Palo Alto Health Care System), Takao Ohyama(VA Palo Alto Health Care System), Carsten Alt(VA Palo Alto Health Care System), Junliang Pan(VA Palo Alto Health Care System), Hajime Suto(Stanford University), Dulce Soler(Millennium Engineering and Integration (United States)), Samantha J. Allen(University of California San Diego), Tracy M. Handel(University of California San Diego), Chang Ho Song(Jeonbuk National University), Stephen J. Galli(Stanford University), Eugene C. Butcher(VA Palo Alto Health Care System)
The Journal of Experimental Medicine
September 15, 2008
Cited by 297Open Access
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Abstract

Mast cells contribute importantly to both protective and pathological IgE-dependent immune responses. We show that the mast cell-expressed orphan serpentine receptor mCCRL2 is not required for expression of IgE-mediated mast cell-dependent passive cutaneous anaphylaxis but can enhance the tissue swelling and leukocyte infiltrates associated with such reactions in mice. We further identify chemerin as a natural nonsignaling protein ligand for both human and mouse CCRL2. In contrast to other "silent" or professional chemokine interreceptors, chemerin binding does not trigger ligand internalization. Rather, CCRL2 is able to bind the chemoattractant and increase local concentrations of bioactive chemerin, thus providing a link between CCRL2 expression and inflammation via the cell-signaling chemerin receptor CMKLR1.


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