华西口腔医学杂志

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3种髓腔穿孔修复材料对人牙周膜成纤维细胞毒性的体外研究

汪莉1,2 尹仕海3 钟素兰1 揭有琼1   

  1. 1.口腔疾病研究国家重点实验室, 四川大学, 四川成都610041;2.双流县第一人民医院口腔科, 四川成都610200;3.四川大学华西口腔医院牙体牙髓病科, 四川成都610041
  • 收稿日期:2009-10-25 修回日期:2009-10-25 出版日期:2009-10-20 发布日期:2009-10-20
  • 通讯作者: 尹仕海,Tel:13308185908
  • 作者简介: 汪莉(1981—),女,四川人,住院医师,硕士
  • 基金资助:

    四川省科技厅支撑资助项目(2008sz0202)

Cytotoxicity evaluation of three kinds of perforation repair materials on human periodontal ligament fibroblasts in vitro

WANG Li1,2, YIN Shi-hai3, ZHONG Su-lan1, JIE You-qiong1   

  1. 1. State Key Laboratory of Oral Diseases,Sichuan University, Chengdu 610041, China; 2. Dept. of Stomatology, Shuangliu First People′s Hospital, Chengdu 610200, China; 3. Dept. of Endodontics, West China College of Stomatology, Sichuan University, Chengdu 610041, China
  • Received:2009-10-25 Revised:2009-10-25 Online:2009-10-20 Published:2009-10-20
  • Contact: YIN Shi-hai,Tel:13308185908

摘要:

目的对三氧化矿物凝聚体(MTA)、Z350纳米复合树脂、银汞合金3种常用髓腔穿孔修复材料对人牙周膜成纤维细胞(HPDLF)毒性进行体外比较研究。方法采用甲基噻唑基四唑(MTT)法研究3种材料对HPDLF增殖的影响,并采用荧光定量聚合酶链反应(PCR)法研究材料对细胞碱性磷酸酶(ALP)和骨钙素(OC)mRNA表达的影响。结果MTA的毒性最小,并能上调HPDLF中ALP mRNA和OC mRNA的表达;Z350的毒性级为1级,能够促进细胞ALP mRNA的表达,对细胞OC mRNA的表达基本无抑制;银汞合金对细胞增殖的抑制作用最大,毒性级为3级,具有中度细胞毒性,对细胞ALP mRNA和OC mRNA表达的抑制最强。结论MTA对HPDLF的毒性最小,并且能促进HPDLF的成骨功能和分化,Z350纳米复合树脂次之,银汞合金的毒性最大,并抑制牙周膜成纤维细胞的分化。

关键词: 髓腔穿孔, 穿孔修复材料, 人牙周膜成纤维细胞, 细胞毒性

Abstract:

Objective To select three kinds of perforation repair materials, mineral trioxide aggregate(MTA), Z350, amalgam. And to evaluate the cytotoxicity of three kinds of perforation repair materials on human periodontal ligament fibroblasts(HPDLF) in vitro. Methods The proliferation of HPDLF to three perforation repair materials were examined by methyl thiazolyl tetrazolium(MTT) assay at 1, 3 and 5 days. The mRNA expression levels of bone -associated alkaline phosphatase(ALP) and osteocalcin(OC) were determined using a real -time quantitative polymerase chain reaction(PCR). Results MTA shew almost no inhibition to HPDLF, the expression of ALP mRNA and OC mRNA in the HPDLF cultured on MTA were higher. Z350 induced a slight inhibition to HPDLF, and the expression of ALP mRNA but there was no difference in the expression of OC mRNA. Cell proliferation was significantly impaired by amalgam with grade 3, and the expression of ALP mRNA and OC mRNA were significantly reduced. Conclusion MTA have minimum cytotoxicity on HPDLF and can promote cell differentiation and regenerate of periodontal tissue. Z350 have lower cytotoxicity on HPDLF. Amalgam show highest cytotoxicity on HPDLF in the three materials and inhibit cells differentiation.

Key words: perforation, perforation repair materials, human periodontal ligament fibroblast, cytotoxicity