首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Novel involvement of miR-522-3p in high-mobility group box 1-induced prostaglandin reductase 1 expression and reduction of phagocytosis
【24h】

Novel involvement of miR-522-3p in high-mobility group box 1-induced prostaglandin reductase 1 expression and reduction of phagocytosis

机译:miR-522-3p在高迁移率组箱中的新增介绍1诱导的前列腺素还原酶1表达和减少吞噬作用

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Resolution of inflammation is important for physiological homeostasis. Chronic inflammatory diseases may be caused by abnormal resolution of inflammation. However, what causes a failure of inflammatory resolution is unclear. Here we investigated the involvement of high mobility group box 1 (HMGB1) protein in the control of inflammatory resolution as an 'anti -resolution factor'. We first confirmed the increased expression of HMGB1 and prostaglandin reductase 1 (PTGR1) in inflammatory conditions and HMGB1-mediated regulation of the expression of PTGR1. The inhibition of phagocytosis by HMGB1 was abrogated by PTGR1 silencing. PTGR1 was a direct target of miR522-3p and its expression was regulated by miRNA-522-3p inhibitor or mimic. Finally, miR-522-3p had an important role in the regulation of PTGR1 expression by HMGB1. The data indicates that HMGB1-miR522-3p-PTGR1 axis may be involved in the abnormal resolution of inflammation and suggests that this mechanism might be a target for modulation of chronic inflammatory disorder. (C) 2017 Elsevier B.V. All rights reserved.
机译:炎症的分辨率对于生理稳态是重要的。慢性炎症疾病可能是由于炎症的异常分辨率引起的。然而,导致炎症分辨率的失败尚不清楚。在这里,我们研究了高迁移率组箱1(HMGB1)蛋白在控制炎症分辨率中作为“抗鉴定因子”的控制的累积。我们首先证实了HMGB1和前列腺素还原酶1(PTGR1)在炎症条件下的表达和HMGB1介导的PTGR1表达调节的增加。通过PTGR1沉默消除了HMGB1的吞噬作用的抑制。 PTGR1是MiR522-3P的直接靶标,其表达由MiRNA-522-3P抑制剂或模拟物调节。最后,miR-522-3p在HMGB1调节PTGR1表达中具有重要作用。数据表明HMGB1-MIR522-3P-PTGR1轴可以参与炎症的异常分辨率,并表明该机制可能是调节慢性炎症疾病的靶标。 (c)2017 Elsevier B.v.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号