华西口腔医学杂志

• 基础研究 • 上一篇    下一篇

牙髓卟啉单胞菌内毒素诱导成骨细胞表达炎症因子的信号通路研究

杨谛1 仇丽鸿1 李任1 李子木1 李琛2   

  1. 1.中国医科大学口腔医院牙体牙髓科;2.中国医科大学口腔医学院中心实验室, 辽宁沈阳110002
  • 收稿日期:2010-04-25 修回日期:2010-04-25 出版日期:2010-04-20 发布日期:2010-04-20
  • 通讯作者: 仇丽鸿,Tel:024-22891701
  • 作者简介:杨谛(1983—),女,内蒙古人,硕士
  • 基金资助:

    辽宁省高等学校科研计划基金资助项目(2008819)

Study of signal transduction pathway in the expression of inflammatory factors stimulated by lipopolysaccharides from Porphyromonas endodontalis in osteoblasts

YANG Di1, QIU Li-hong1, LI Ren1, LI Zi-mu1, LI Chen2   

  1. 1. Dept. of Endodontics, School of Stomatology, China Medical University, Shenyang 110002, China; 2. Central Laboratory, School of Stomatology, China Medical University, Shenyang 110002, China
  • Received:2010-04-25 Revised:2010-04-25 Online:2010-04-20 Published:2010-04-20
  • Contact: QIU Li-hong,Tel:024-22891701

摘要:

目的检测细胞外信号调节激酶(ERK)1/2和p38丝裂原活化蛋白激酶抑制剂对牙髓卟啉单胞菌内毒素(LPS)诱导成骨细胞白细胞介素(IL)-1β mRNA和IL-6 mRNA的影响,探讨根尖周病变牙槽骨吸收的可能病理机制。方法成骨细胞MG-63经PD98059和SB203580预处理1 h后,加入牙髓卟啉单胞菌LPS作用6 h,应用逆转录聚合酶链反应(RT-PCR)检测IL-1β mRNA和IL-6 mRNA的表达水平。结果PD98059预处理后,牙髓卟啉单胞菌LPS诱导MG-63表达IL-1β mRNA的水平下降。SB203580预处理后,牙髓卟啉单胞菌LPS诱导MG-63表达IL-1β mRNA和IL-6 mRNA水平均下降。结论牙髓卟啉单胞菌LPS诱导MG-63细胞表达IL-1β mRNA依赖ERK1/2和p38MAPK信号转导通路,表达IL-6 mRNA依赖p38MAPK信号转导通路。

关键词: 牙髓卟啉单胞菌, 内毒素, 成骨细胞, 细胞外信号调节激酶1/2, p38丝裂原活化蛋白激酶

Abstract:

Objective To quantify the interleukin(IL)-1β mRNA and IL-6 mRNA expression induced by lipopolysaccharides(LPS) extracted from Porphyromonas endodontalis(P.endodontalis) in osteoblasts, and to relate P. endodontalis LPS to the bone resorptive pathogenesis in the lesions of chronic apical periodontitis. Methods MG63 cells was pretreated with PD98059 or SB203580 for 1 h and then treated with P.endodontalis LPS for 6 h. The expression of IL-1β mRNA and IL-6 mRNA were detected by reverse transcription polymerase chain reaction(RTPCR) technique. Results The production of IL-1β mRNA induced by P.endodontalis LPS decreased in osteoblasts pretreated with PD98059. Both of the production of IL-1β mRNA and IL-6 mRNA induced by P.endodontalis LPS decreased in osteoblasts pretreated with SB203580. Conclusion The synthesis of IL-1β mRNA stimulated by P.endodontalis LPS in MG63 probably occur via extracellular signal-regulated kinase(ERK) 1/2 and p38 mitogen activated protein kinase(MAPK) signal transduction system. The synthesis of IL-6 mRNA stimulated by P.endodontalis LPS in MG63 probably occur via p38MAPK signal transduction system.

Key words: Porphyromonas endodontalis, lipopolysaccharides, osteoblasts, extracellular signal-regulated kinase 1/2, p38 mitogen activated protein kinase