4.5 Article

Decreased IL-10 expression in stefin B-deficient macrophages is regulated by the MAP kinase and STAT-3 signaling pathways

期刊

FEBS LETTERS
卷 588, 期 5, 页码 720-726

出版社

WILEY
DOI: 10.1016/j.febslet.2014.01.015

关键词

Cystatin; Interleukin-10; Lipopolysaccharide; Macrophage; MAP-kinase; Nitric oxide

资金

  1. Slovenian Research Agency [J3-0612]
  2. Grant CEA France-Slovenia
  3. Slovenian Young researcher program
  4. [P-0140]

向作者/读者索取更多资源

Innate immune responses are tightly regulated to avoid excessive activation and subsequent inflammatory damage to the host, and interleukin-10 (IL-10) plays a crucial role in preventing inflammation. Stefin B (cystatin B) is an endogenous inhibitor of cysteine proteinases. In stefin B-deficient bone marrow-derived macrophages (BMDMs), we detected an increase in the induction of the LPS-induced pro-inflammatory signal nitric oxide (NO) but decreased IL-10 expression. The phosphorylation of ERK and p38 MAP-kinases was significantly decreased in stefin B-deficient macrophages, as was STAT-3 phosphorylation. These findings show that stefin B influences the expression of anti-inflammatory IL-10 in response to the TLR4 agonist LPS. (c) 2014 Federation of European Biochemical Societies. Published by Elsevier B. V. 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

4.5
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