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山东大学学报(医学版) ›› 2015, Vol. 53 ›› Issue (6): 44-47.doi: 10.6040/j.issn.1671-7554.0.2014.490

• 基础医学 • 上一篇    下一篇

MRP8通过NF-κB信号通路调控痛风细胞模型中IL-1β的表达

赵璐1, 孙俊波2, 魏桂梅1   

  1. 1. 河南中医学院第三附属医院内分泌科, 河南 郑州 450008;
    2. 河南省中医院内科, 河南 郑州 450002
  • 收稿日期:2014-07-27 修回日期:2015-01-23 出版日期:2015-06-10 发布日期:2015-06-10
  • 通讯作者: 孙俊波。E-mail:13838099075@139.com E-mail:13838099075@139.com

MRP8 regulates expression of IL-1β in gout cell model by NF-κB signaling pathway

ZHAO Lu1, SUN Junbo2, WEI Guimei1   

  1. 1. Department of Endocrinology, Third Affiliated Hospital of Henan College of Traditional Chinese Medicine, Zhengzhou 450008, Henan, China;
    2. Department of Medicine, Henan Province Hospital of Traditional Chinese Medicine, Zhengzhou 450002, Henan, China
  • Received:2014-07-27 Revised:2015-01-23 Online:2015-06-10 Published:2015-06-10

摘要: 目的 研究髓样相关蛋白8(MRP8)在痛风中的作用及其机制。方法 单钠尿酸盐(MSU)结晶诱导巨噬细胞产生痛风模型,检测诱导后巨噬细胞中MRP8的水平。MRP8 siRNA转染巨噬细胞,Western blotting检测沉默效果及MRP8沉默对核转录因子κB(NF-κB)信号通路中的NF-κB和NF-κB抑制蛋白(I-κB)表达的影响,ELISA法检测MRP8沉默对炎性因子白细胞介素-1β(IL-1β)分泌的影响。结果 MSU可诱导巨噬细胞高表达MRP8(P<0.01);MRP8 siRNA转染能有效干扰巨噬细胞中MRP8的表达。MPR8沉默后巨噬细胞中IL-1β的分泌明显减少(P<0.05),同时NF-κB表达下调,I-κB表达上调。结论 MRP8参与MSU诱导痛风的炎性因子IL-1β的释放过程,且有可能通过NF-κB信号通路调控IL-1β的分泌来实现。

关键词: 巨噬细胞, 髓样相关蛋白8, 白细胞介素-1β, 核转录因子κB, 核转录因子κB抑制蛋白

Abstract: Objective To explore the effect and underlying mechanism of myeloid-related protein 8 (MRP8) on gout. Methods Gout model in macrophages was induced by monosodium urate (MSU), and the expression of MRP8 in these model cells was detected by ELISA. Then, MRP8 siRNA was transferred into macrophage, and the effectiveness was verified by Western blotting. The influences of silenced MRP8 on the secretion of interleukin-1β (IL-1β), nuclear transcription factor-κB (NF-κB) and inhibitor of nuclear transcription factor-κB (I-κB) expressions in macrophages were detected by ELISA and Western blotting. Results The expression of MRP8 in macrophages increased after MSU induction (P<0.01) and MPR siRNA could silence MPR8 expression effectively. After the silence of MPR8, the IL-1β secretion decreased (P<0.05), NF-κB expression was down-regulated, while I-κB espression was up-regulated in macrophages. Conclusion MRP-8 participates in the process of IL-1β release in MSU-induced macrophages gout model, which may be regulated by NF-κB signal pathway.

Key words: Nuclear transcription factor-κB, Interleukin-1β, Inhibitor of nuclear transcription factor-κB, Myeloid-related protein 8, Macrophage

中图分类号: 

  • R589
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