Fc receptor γ-chain, a constitutive component of the IL-3 receptor, is required for IL-3-induced IL-4 production in basophils

被引:76
作者
Hida, Shigeaki [1 ]
Yamasaki, Sho [2 ]
Sakamoto, Yuzuru [1 ]
Takamoto, Masaya [1 ]
Obata, Kazushige [3 ]
Takai, Toshiyuki [4 ]
Karasuyama, Hajime [3 ]
Sugane, Kazuo [1 ]
Saito, Takashi [2 ]
Taki, Shinsuke [1 ]
机构
[1] Shinshu Univ, Grad Sch Med, Dept Immunol & Infect Dis, Matsumoto, Nagano 3908621, Japan
[2] RIKEN, Res Ctr Allergy & Immunol, Lab Cell Signaling, Yokohama, Kanagawa 2300045, Japan
[3] Tokyo Med & Dent Univ, Grad Sch, Dept Immune Regulat, Tokyo 1138519, Japan
[4] Tohoku Univ, Dept Expt Immunol, Inst Dev Aging & Canc, Sendai, Miyagi 9808575, Japan
基金
日本学术振兴会;
关键词
SIGNAL-TRANSDUCTION; TYROSINE KINASE; BETA-CHAIN; T-CELLS; CYTOKINE; SYK; MECHANISM; ITAM; DIFFERENTIATION; MICE;
D O I
10.1038/ni.1686
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Fc receptor common gamma-chain (FcR gamma) is a widely expressed adaptor bearing an immunoreceptor tyrosine-based activation motif (ITAM) that transduces activation signals from various immunoreceptors. We show here that basophils lacking FcR gamma developed normally and proliferated efficiently in response to interleukin 3 (IL-3) but were very impaired in IL-3-induced production of IL-4 and in supporting T helper type 2 differentiation. Through its transmembrane portion, FcR gamma associated constitutively with the common beta-chain of the IL-3 receptor and signaled by recruiting the kinase Syk. Retrovirus-mediated complementation demonstrated the essential function of the ITAM of FcR gamma in IL-3 signal transduction. Our results identify a previously unknown mechanism whereby FcR gamma functions to 'route' selective cytokine-triggered signals into the ITAM-mediated IL-4 production pathway.
引用
收藏
页码:214 / 222
页数:9
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