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(h PDLCs)A20siRNA、慢病毒,获得A20沉默/过表达h PDLCs,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h PDLCs 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h PDLCs RANKL表达。
Objective To investigate the potential function of A20 on modulating RANKL expression of the human periodontal liga- ment 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 immu- nosorbent 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), simi- lar 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.
出处
《口腔医学》
CAS
2016年第6期489-493,共5页
Stomatology