...
首页> 外文期刊>Biochemical and Biophysical Research Communications >Mitogen-activated protein kinases and phosphatidylinositol 3-kinase are involved in Prevotella intermedia-induced proinflammatory cytokines expression in human periodontal ligament cells.
【24h】

Mitogen-activated protein kinases and phosphatidylinositol 3-kinase are involved in Prevotella intermedia-induced proinflammatory cytokines expression in human periodontal ligament cells.

机译:丝裂原活化的蛋白激酶和磷脂酰肌醇3-激酶参与了人体内牙周膜细胞中普氏杆菌介导的促炎细胞因子的表达。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Chronic periodontitis is an inflammatory disease affecting periodontal connective tissues and alveolar bone. Proinflammatory mediators induced by periodontal pathogens play vital roles in the initiation and progression of the disease. In this study, we examined whether Prevotella intermedia induces proinflammatory cytokines expression in human periodontal ligament cells (hPDLs). The mRNA expression and protein production were determined by reverse transcription-polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbant assay (ELISA) respectively. P. intermedia treatment dose- and time-dependently increased IL-6, IL-8 and M-CSF, but not IL-1beta and TNF-alpha mRNA expression and protein secretion. Preincubation of hPDLs with extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK), p38 kinase and phosphatidylinositol 3-kinase (PI3K) inhibitors PD98059, SP600125, SB203580 and LY294002 resulted in significant reduction in P. intermedia-induced IL-6, IL-8 and M-CSF expression. Blocking the synthesis of prostaglandin E(2) (PGE(2)) by indomethacin also abolished the stimulatory effects of P. intermedia on cytokines expression. Our results indicate that P. intermedia induces proinflammatory cytokines through MAPKs and PI3K signaling pathways, and PGE(2) is involved in the P. intermedia-induced proinflammatory cytokines upregulation.
机译:慢性牙周炎是一种炎症性疾病,会影响牙周结缔组织和牙槽骨。牙周病原体诱导的促炎介质在疾病的发生和发展中起着至关重要的作用。在这项研究中,我们检查了中间型普氏杆菌是否在人牙周膜细胞(hPDLs)中诱导促炎细胞因子表达。分别通过逆转录-聚合酶链反应(RT-PCR)和酶联免疫吸附法(ELISA)测定mRNA的表达和蛋白质的产生。中间疟原虫处理剂量和时间依赖性地增加IL-6,IL-8和M-CSF,但不增加IL-1beta和TNF-αmRNA表达和蛋白质分泌。 hPDL与细胞外信号调节激酶(ERK),c-Jun N端激酶(JNK),p38激酶和磷脂酰肌醇3-激酶(PI3K)抑制剂PD98059,SP600125,SB203580和LY294002的预孵育导致中间假单胞菌的显着减少-诱导的IL-6,IL-8和M-CSF表达。吲哚美辛阻止前列腺素E(2)(PGE(2))的合成,也取消了中间P.对细胞因子表达的刺激作用。我们的结果表明,中间媒介通过MAPKs和PI3K信号通路诱导促炎细胞因子,而PGE(2)参与中间媒介诱导的促炎细胞因子上调。

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