Prostaglandin D2 Selectively Induces Chemotaxis in T Helper Type 2 Cells, Eosinophils, and Basophils via Seven-Transmembrane Receptor Crth2

Author:

Hirai Hiroyuki12,Tanaka Kazuya1,Yoshie Osamu3,Ogawa Kazuyuki1,Kenmotsu Kazumi1,Takamori Yasushi1,Ichimasa Michiko4,Sugamura Kazuo5,Nakamura Masataka6,Takano Shoichi1,Nagata Kinya1

Affiliation:

1. R&D Center, BML, Saitama 350-1101, Japan

2. Graduate School of Science and Engineering, Faculty of Science, Ibaraki University, Ibaraki 310-8512, Japan

3. Department of Bacteriology, Kinki University School of Medicine, Osaka 589-8511, Japan

4. Department of Environmental Sciences, Faculty of Science, Ibaraki University, Ibaraki 310-8512, Japan

5. Department of Microbiology and Immunology, Tohoku University School of Medicine, Miyagi 980-8575, Japan

6. Human Gene Sciences Center, Tokyo Medical and Dental University, Tokyo 113-8510, Japan

Abstract

Prostaglandin (PG)D2, which has long been implicated in allergic diseases, is currently considered to elicit its biological actions through the DP receptor (DP). Involvement of DP in the formation of allergic asthma was recently demonstrated with DP-deficient mice. However, proinflammatory functions of PGD2 cannot be explained by DP alone. We show here that a seven-transmembrane receptor, CRTH2, which is preferentially expressed in T helper type 2 (Th2) cells, eosinophils, and basophils in humans, serves as the novel receptor for PGD2. In response to PGD2, CRTH2 induces intracellular Ca2+ mobilization and chemotaxis in Th2 cells in a Gαi-dependent manner. In addition, CRTH2, but not DP, mediates PGD2-dependent cell migration of blood eosinophils and basophils. Thus, PGD2 is likely involved in multiple aspects of allergic inflammation through its dual receptor systems, DP and CRTH2.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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