›› 2016, Vol. 36 ›› Issue (6): 489-493.

• 基础研究 • 上一篇    下一篇

A20对IL-17介导人牙周膜细胞RANKL表达影响

叶宇1,俞文伟1,陈旭2,茅飞飞1,徐艳3,李璐1   

  1. 1. 南京医科大学口腔疾病研究江苏省重点实验室
    2. 江苏省口腔疾病研究重点实验室
    3. 南京医科大学附属口腔医院牙周科
  • 收稿日期:2015-12-24 修回日期:2016-02-27 出版日期:2016-06-28 发布日期:2016-06-30
  • 通讯作者: 徐艳 E-mail:yanxu@njmu.edu.cn
  • 基金资助:
    国家自然科学基金;国家自然科学基金;江苏省高校优势学科建设工程

Effect of A20 on modulating RANKL expression of human periodontal ligament cells (hPDLCs) through IL-17

  • Received:2015-12-24 Revised:2016-02-27 Online:2016-06-28 Published:2016-06-30

摘要: [摘要] 目的 探究A20对IL-17调控人牙周膜细胞表面RANKL表达的影响。方法 转染人牙周膜细胞(hPDLCs)A20siRNA、慢病毒,获得A20沉默/过表达hPDLCs,分为沉默组、正常组、过表达组,IL-17(50 ng/ml)刺激一定时间,ELISA,PCR ,Western-blot检测RANKL表达。结果 A20沉默组的hPDLCs RANKL蛋白表达水平较正常对照组高,A20过表达组较正常对照组低,IL-17(50ng/ml)刺激下,A20沉默组较正常对照组RANKL表达水平高,过表达组较正常对照组低。结论 本研究首次发现A20可能参与调控IL-17引起的hPDLCs RANKL表达。

关键词: 牙周膜成纤维细胞, 白介素17 , 肿瘤坏死因子α诱导蛋白, 细胞核因子κB 受体活化因子配体

Abstract: Abstract: Objective To investigate the potential function of A20 on modulating RANKL expression of the human periodontal ligament cells (hPDLCs) regulated by IL-17. Methods HPDLCs were transfected of A20siRNA and slow virus, and then hPDLCs by suppression/over-expression of A20 were obtained, which were divided into suppression group, control group and over-expression group. Treated with IL-17 (50 ng/ml) for certain time, protein and mRNA levels of RANKL were determined by enzyme-linked immunosorbent assays (ELISA), real-time PCR (RT-PCR) and western blotting. Results Suppression/over-expression of A20 in hPDLCs increased/decreased the expression of RANKL protein compared to the control group. Upon the stimulation of IL-17 (50ng/ml), similar results were observed in the three groups of hPDLCs. Conclusion Our study revealed for the first time that IL-17 induced RANKL expression of hPDLCs may be interfered by A20.

Key words: periodontal ligament cells, IL-17, tumor necrosis factor alpha-induced protein3, RANKL

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