Dectin-1 stimulates IL-33 expression in dendritic cells via upregulation of IRF4

被引:6
|
作者
Wang, Dongjiao [1 ]
Gao, Sujun [2 ]
Chen, Jintong [3 ]
Zhao, Yinghua [3 ]
Jiang, Yuxue [3 ]
Chu, Xiao [3 ]
Wang, Xiaohua [4 ]
Liu, Ning [1 ]
Qin, Tianxue [2 ]
Yi, Qing [3 ,5 ]
Yue, Ying [1 ]
Wang, Siqing [3 ]
机构
[1] Jilin Univ, Hosp 1, Dept Gynecol Oncol, Changchun 130061, Jilin, Peoples R China
[2] Jilin Univ, Hosp 1, Dept Hematol, Changchun 130061, Jilin, Peoples R China
[3] Jilin Univ, Hosp 1, Dept Canc Immunol, Changchun 130061, Jilin, Peoples R China
[4] Linhai First Peoples Hosp, Dept Internal Med, Linhai 317000, Zhejiang, Peoples R China
[5] Cleveland Clin, Lerner Res Inst, Dept Canc Biol, Cleveland, OH 44195 USA
基金
中国国家自然科学基金;
关键词
TUMOR-IMMUNITY; TH9; CELLS; INTERLEUKIN-33; IMMUNOTHERAPY; INFLAMMATION; RESPONSES; VACCINES; PATHWAY; ALLERGY; ROLES;
D O I
10.1038/s41374-018-0047-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Interleukin-33 (IL-33) is a potent contributor to antiviral immune responses and antitumor immunity. We recently discovered that IL-33 is overexpressed in dectin-1-activated dendritic cells (DCs). However, mechanisms of dectin-1-induced IL-33 expression in DCs remain elusive. Curdlan, an agonist of dectin-1, was used to mature DCs in this study. We found that dectin-1-induced IL-33 expression in DCs relies on Syk and Raf-1 pathways. By using nuclear factor (NF)-kappa B inhibitors, we also found that dectin-1-induced IL-33 expression relies on NF-kappa B signaling. Furthermore, through Syk/Raf-1-NF-kappa B pathway, dectin-1 signaling stimulates DCs to overexpress interferon regulatory factor 4 (IRF4), which directly upregulates the expression of IL-33 in dectin-1-activated DCs. Thus, our study provides new insights into the mechanisms of dectin-1induced IL-33 expression in DCs and may provide new targets for improving DC-based cancer immunotherapy.
引用
收藏
页码:708 / 714
页数:7
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