The putative tumor suppressor Zc3h12d modulates toll-like receptor signaling in macrophages

被引:40
|
作者
Huang, Shengping [1 ,2 ]
Qi, Dongfei [1 ,2 ]
Liang, Jian [3 ]
Miao, Ruidong [1 ,2 ]
Minagawa, Kentaro [4 ]
Quinn, Tim [1 ,2 ]
Matsui, Toshimitsu [4 ]
Fan, Daping [5 ]
Liu, Jianguo [6 ]
Fu, Mingui [1 ,2 ]
机构
[1] Univ Missouri, Sch Med, Shock Trauma Res Ctr, Kansas City, MO 64108 USA
[2] Univ Missouri, Sch Med, Dept Basic Med Sci, Kansas City, MO 64108 USA
[3] Univ Cent Florida, Burnett Sch Biol Sci, Coll Med, Orlando, FL 32816 USA
[4] Kobe Univ, Grad Sch Med, Kobe, Hyogo 657, Japan
[5] Univ S Carolina, Dept Cell Biol & Anat, Columbia, SC 29209 USA
[6] St Louis Univ, Sch Med, Dept Internal Med, St Louis, MO 63104 USA
关键词
Macrophage; Toll-like receptor; Signal transduction; JNK; NF-kappa B; ATHEROSCLEROTIC LESION DEVELOPMENT; FOLLICULAR LYMPHOMA; CELL LYMPHOMA; KAPPA-B; ACTIVATION; DISEASE; GENE;
D O I
10.1016/j.cellsig.2011.10.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Toll-like receptors (TLR) are pivotal in macrophage activation. The molecular mechanisms controlling TLR signaling and macrophage activation are not completely understood. Zc3h12d is originally identified as a possible tumor suppressor gene. However, its function remains unknown. We here report that Zc3h12d negatively regulates TLR signaling and macrophage activation. Zc3h12d was enriched in spleen, lung and lymph node. In macrophages, the expression of Zc3h12d was remarkably induced by TLR ligands through JNK and NF-kappa B signal pathways. On the other hand, overexpression of Zc3h12d significantly inhibited TLR2 and TLR4 activation-induced JNK, ERK and NF-kappa B signaling as well as macrophage inflammation. Similar to Zc3h12a/MCPIP1. Zc3h12d also decreased the global cellular protein ubiquitination. These findings suggest that Zc3h12d is a novel negative feedback regulator of TLR signaling and macrophage activation and thus may play a role in host immunity and inflammatory diseases. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:569 / 576
页数:8
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