›› 2014, Vol. 5 ›› Issue (1): 15-18.

• 论著 • 上一篇    下一篇

青霉素和链霉素对炎症牙髓干细胞的增殖、成牙成骨分化能力及TNF-α表达的影响

王利娟1,俞艳1,曹灵2,薛晶1,张光东3,于金华1   

  1. 1. 南京医科大学口腔医学研究所
    2. 本院
    3. 南京医科大学口腔医学院
  • 收稿日期:2013-12-13 修回日期:2014-03-11 出版日期:2014-03-25 发布日期:2014-03-31
  • 通讯作者: 张光东 E-mail:edg_zhang@njmu.edu.cn

Effect of Penicillin-Streptomycin on the proliferation, odonto-and osteogenic differentiation potential and the expression of the inflammatory cytokines TNF-α of the inflamed human dental pulp stem cells

  • Received:2013-12-13 Revised:2014-03-11 Online:2014-03-25 Published:2014-03-31

摘要: 目的:探讨青霉素和链霉素对炎症牙髓干细胞的增殖、成牙成骨分化能力及肿瘤坏死因子α(tumor necrosis factor α,TNF-α)表达的影响。方法:采用酶消化法分离培养炎症牙髓干细胞,采用甲基噻唑基四唑(MTT)比色法、碱性磷酸酶活性检测、Western Blot及实时定量RT-PCR等方法分析青霉素和链霉素作用于炎症牙髓干细胞后,其增殖和成牙成骨分化指标(核心结合因子、牙本质涎蛋白/牙本质涎磷蛋白、骨钙素)及TNF-α表达的变化。结果:青霉素和链霉素作用于炎症牙髓干细胞后,与未加抗生素的培养组细胞的增殖能力及成骨/成牙相关蛋白、基因的表达无明显差异(P>0.05),而TNF-α的表达则低于普通培养组(P <0.01)。结论:青霉素和链霉素降低炎症牙髓干细胞的炎性因子TNF-α表达,对细胞的增殖及成牙/成骨分化能力无明显影响。

Abstract: Objective:To observe the effects of Penicillin-Streptomycin on the proliferation, odonto-and osteogenic differentiation and the expression of the inflammatory cytokines of inflamed human dental pulp stem cells (iDPSCs) in vitro. Methods:iDPSCs were isolated from inflamed human dental pulp and cultured respectively in alpha minimum essential medium(α-MEM) or containing 100U/ml Penicillin-Streptomycin. The proliferation ability of iDPSCs was evaluated by MTT colorimetric assay. Alkaline phosphotase (ALP) activity, real-time RT-PCR and Western blot were used to examine the odonto/osteogenic potential-the the expression of RUNX2/RUNX2,DSP/DSPP,OCN/OCN and the expression of TNF-α of iDPSCs. Results:MTT assay showed that 100U/ml Penicillin-Streptomycin had no effect on the proliferation of iDPSCs, ALP activity assay, real-time RT-PCR and Western blot showed that there was no difference between Penicillin-Streptomycin group and α-MEM group (P>0.05). The expression of TNF-α decreased in Penicillin-Streptomycin group (P<0.01). Conclusions:Penicillin-Streptomycin significantly suppressed the expression of inflammatory cytokines in inflammatory dental pulp stem cells, and has no noticeable effect on the proliferation and differentiation of the cells.