Critical Role of p38 and GATA3 in Natural Helper Cell Function

被引:126
作者
Furusawa, Jun-ichi [1 ,2 ]
Moro, Kazuyo [1 ,2 ,3 ,4 ]
Motomura, Yasutaka [5 ,6 ]
Okamoto, Kazuo [7 ,8 ,9 ,10 ]
Zhu, Jinfang [11 ]
Takayanagi, Hiroshi [7 ,8 ,9 ,10 ]
Kubo, Masato [5 ,6 ]
Koyasu, Shigeo [1 ,2 ]
机构
[1] Keio Univ, Sch Med, Dept Microbiol & Immunol, Tokyo 1608582, Japan
[2] RIKEN Ctr Integrat Med Sci, RCAI, Lab Immune Cell Syst, Yokohama, Kanagawa 2300045, Japan
[3] Japan Sci & Technol Agcy, Precursory Res Embryon Sci & Technol, Tokyo 1020076, Japan
[4] Yokohama City Univ, Grad Sch Med Life Sci, Dept Med Life Sci, Div Immunobiol, Yokohama, Kanagawa 2300045, Japan
[5] RIKEN Ctr Integrat Med Sci, RCAI, Lab Cytokine Regulat, Yokohama, Kanagawa 2300045, Japan
[6] Tokyo Univ Sci, Res Inst Biomed Sci, Div Mol Pathol, Chiba 2780022, Japan
[7] Japan Sci & Technol Agcy, Exploratory Res Adv Technol, Takayanagi Osteonetwork Project, Tokyo 1020076, Japan
[8] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Cell Signaling, Tokyo 1138549, Japan
[9] Univ Tokyo, Grad Sch Med, Dept Immunol, Tokyo 1130033, Japan
[10] Univ Tokyo, Fac Med, Tokyo 1130033, Japan
[11] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
基金
日本学术振兴会; 日本科学技术振兴机构; 美国国家卫生研究院;
关键词
INNATE LYMPHOID-CELLS; TRANSCRIPTION FACTOR GATA3; ALLERGIC INFLAMMATION; ADAPTIVE IMMUNITY; TYPE-2; IMMUNITY; NKP46(+) CELLS; FAMILY-MEMBER; CUTTING EDGE; FACTOR E4BP4; MAST-CELLS;
D O I
10.4049/jimmunol.1300379
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Natural helper (NH) cells, a member of Lin(-)IL-2R(+)IL-7R(+)IL-25R(+)IL-33R(+)GATA3(+) group 2 innate lymphoid cell subset, are characterized by the expression of transcription factors GATA3 and ROR alpha and production of large amounts of Th2 cytokines such as IL-5, IL-6, and IL-13 upon IL-33 stimulation or a combination of IL-2 and IL-25. We have studied the signal transduction pathways critical for the cytokine expression and development of NH cell. Either stimulation with IL-33 or a combination of IL-2 and IL-25 induced p38 activation and phosphorylation of GATA3 in NH cells, and the phosphorylated form of GATA3 bound to the IL-5 and IL-13 promoters. All these events were blocked by SB203580, a p38 inhibitor. Inhibition of p38 also blocked IL-6 production. The mature NH cells lacking Gata3 were impaired in the proliferation and production of IL-5 and IL-13, but not IL-6, indicating that both p38 and GATA3 are critical for the proliferation and production of IL-5 and IL-13 and that the mechanisms downstream of p38 differ between IL-6 and IL-5/IL-13. In contrast, the NH cells lacking RORa showed no impairment in the proliferation and cytokine production, indicating that GATA3 but not ROR alpha plays a pivotal role in the effector functions of mature NH cell. However, deletion of either GATA3 or ROR alpha in hematopoietic stem cells severely blocked the development into NH cells. Our results demonstrate the important roles of p38 and GATA3 in NH cell functions.
引用
收藏
页码:1818 / 1826
页数:9
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