CD137 Regulates NFATc1 Expression in Mouse VSMCs through TRAF6/NF-κB p65 Signaling Pathway

被引:13
作者
Yan, Jinchuan [1 ]
Yin, Yunjie [1 ]
Zhong, Wei [1 ]
Wang, Cuiping [1 ]
Wang, Zhongqun [1 ]
机构
[1] Jiangsu Univ, Affiliated Hosp, Dept Cardiol, Zhenjiang 212001, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
KAPPA-B PATHWAY; T-CELLS; ACTIVATION; MICE; ATHEROSCLEROSIS; DISEASE; 4-1BB; DOWNSTREAM; RECEPTOR; TRAF1;
D O I
10.1155/2015/639780
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Our previous study proved that CD137-CD137L interaction can regulate the expression of NFATc1. Here, we investigated whether CD137 signaling regulates the expression of NFATc1 in mice VSMCs through TRAF6/NF-kappa B p65 pathway. Data shows that the CD137 expression can be stimulated by TNF-alpha in a time-dependent manner in mouse VSMCs. Knockdown of TRAF6 by siTRAF6 significantly attenuated agonist-CD137mAb induced increase of NF-kappa B p65 and NFATc1 in VSMCs. Pretreatment with a NF-kappa B inhibitor PDTC for 30 min inhibited the expression of p-p65 in both cytoplasm and nucleus in VSMCs. Thus, the protein level of NFATc1 can be suppressed through inhibition of p-p65. Finally, we also show that the levels of IL-2 and IL-6 can be increased by agonist-CD137 stimulation and decreased when NFATc1 was suppressed. Our data suggest that activated CD137 signaling regulates the expression of NFATc1 and its downstream factors through TRAF6/NF-kappa B p65 pathways in VSMCs. These findings provide a novel target for treatment of atherosclerosis.
引用
收藏
页数:10
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