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

Author:

Zabel Brian A.1,Nakae Susumu2,Zúñiga Luis1,Kim Ji-Yun1,Ohyama Takao1,Alt Carsten1,Pan Junliang1,Suto Hajime2,Soler Dulce3,Allen Samantha J.4,Handel Tracy M.4,Song Chang Ho25,Galli Stephen J.26,Butcher Eugene C.1

Affiliation:

1. Laboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, and Center for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, CA 94304

2. Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305

3. Inflammation Department, Millennium Pharmaceuticals, Cambridge, MA 02139

4. Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA 92093

5. Department of Anatomy, Chonbuk National University Medical School, Jeonju, Republic of Korea

6. Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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