Prostaglandin D2 selectively induces chemotaxis in T helper type 2 cells, eosinophils, and basophils via seven-transmembrane receptor CRTH2

被引:921
作者
Hirai, H
Tanaka, K
Yoshie, O
Ogawa, K
Kenmotsu, K
Takamori, Y
Ichimasa, M
Sugamura, K
Nakamura, M
Takano, S
Nagata, K
机构
[1] BML, R&D Ctr, Kawagoe, Saitama 3501101, Japan
[2] Ibaraki Univ, Grad Sch Sci & Engn, Mito, Ibaraki 3108512, Japan
[3] Ibaraki Univ, Fac Sci, Dept Environm Sci, Mito, Ibaraki 3108512, Japan
[4] Kinki Univ, Sch Med, Dept Bacteriol, Sayama, Osaka 5898511, Japan
[5] Tohoku Univ, Sch Med, Dept Microbiol & Immunol, Sendai, Miyagi 9808575, Japan
[6] Tokyo Med & Dent Univ, Human Gene Sci Ctr, Tokyo 1138510, Japan
关键词
prostanoid receptor; G alpha i-type G protein; T cells; cell migration; allergic inflammation;
D O I
10.1084/jem.193.2.255
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Prostaglandin (PG)D-2, 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 PGD, 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 PGD(2). In response to PGD(2), CRTH2 induces intracellular Ca2+ mobilization and chemotaxis in Th2 cells in a G alphai-dependent manner. In addition, CRTH2, but not DP, mediates PGD(2)-dependent cell migration of blood eosinophils and basophils. Thus, PGD(2) is likely involved in multiple aspects of allergic inflammation through its dual receptor systems, DP and CRTH2.
引用
收藏
页码:255 / 261
页数:7
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