4.6 Article

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

期刊

CELLULAR SIGNALLING
卷 24, 期 2, 页码 569-576

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2011.10.011

关键词

Macrophage; Toll-like receptor; Signal transduction; JNK; NF-kappa B

资金

  1. American Heart Association BGIA
  2. National Institute of Health [HL-098794, CA-137126, AR-055353, HL-106325, RR-016434]
  3. Grants-in-Aid for Scientific Research [23791081, 22591037] Funding Source: KAKEN

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据