Induction of IL-12 production by the activation of discoidin domain receptor 2 via NF-κB and JNK pathway

被引:16
|
作者
Poudel, Barun [1 ,2 ]
Ki, Hyeon-Hui [1 ,2 ]
Lee, Young-Mi [3 ]
Kim, Dae-Ki [1 ,2 ]
机构
[1] Chonbuk Natl Univ, Sch Med, Dept Immunol, Jeonju 561756, Jeonbuk, South Korea
[2] Chonbuk Natl Univ, Sch Med, Inst Med Sci, Jeonju 561756, Jeonbuk, South Korea
[3] Wonkwang Univ, Dept Oriental Pharm, Coll Pharm, Iksan 570749, Jeonbuk, South Korea
基金
新加坡国家研究基金会;
关键词
DDR2; Interleukin; 12; Collagen I; NF-kappa B; JNK; Murine dendritic cells; DENDRITIC CELLS; INTERLEUKIN-12; PRODUCTION; INTERFERON-GAMMA; IFN-GAMMA; T-CELLS; COLLAGEN; CYTOKINE; KINASE; MICE; MACROPHAGES;
D O I
10.1016/j.bbrc.2013.03.118
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We investigated the mechanism involving discoidin domain receptor 2 (DDR2) mediated production of interleukin 12 (IL-12). When compared to control, collagen I upregulated the IL-12 luciferase activity on DDR2 expressing cells. Collagen I induced the phosphorylation of DDR2 and enhanced the phosphorylation of mitogen activated protein kinase (MAPK) kinases. In addition, NF-kappa B binding activity was enhanced when the cells expressing NF-kappa B reporter were exposed to collagen I. Moreover, when IL-12 reporter transfected cells were treated with biochemical inhibitors of c-Jun N-terminal kinase (JNK) and NF-kappa B, collagen-induced IL-12 promoter activity was significantly downregulated in comparison to non-treated cells. Similarly, confirmatory experiments on murine dendritic cells revealed that IL-12 promoter activity is dose dependently downregulated upon NF-kappa B and JNK inhibitor treatment on collagen I stimulation. In summary, DDR2 is involved in the collagen I-induced IL-12 production via NF-kappa B and JNK pathway. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:584 / 588
页数:5
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