中国组织工程研究 ›› 2011, Vol. 15 ›› Issue (2): 265-268.doi: 10.3969/j.issn.1673-8225.2011.02.018

• 组织构建与生物活性因子 tissue construction and bioactive factors • 上一篇    下一篇

血小板衍化生长因子β对体外人牙周膜细胞增殖分化的影响

林景广,亓  峰,葛一鸣,韩  杰   

  1. 辽宁医学院附属第二医院暨附属口腔医院,辽宁省锦州市 121000
  • 收稿日期:2010-07-14 修回日期:2010-08-28 出版日期:2011-01-08 发布日期:2011-01-08
  • 作者简介:林景广,男,1963年生,辽宁省锦州市人,汉族,1986年中国医科大学毕业,主任医师,教授,从事牙体牙髓及牙周方面的研究。 379311389@qq.com;linjg138@sohu. com
  • 基金资助:

    辽宁教育厅科学技术研究项目(2008339),项目名称:血小板衍化生长因子β对体外人牙周膜细胞增殖分化的影响。

Effect of platelet-derived growth factor beta on in vitro proliferation and differentiation of human periodontal ligament cells   

Lin Jing-guang, Qi Feng, Ge Yi-ming, Han Jie   

  1. Second Affiliated Hospital of Liaoning Medical University, Stomatology Hospital of Liaoning Medical University, Jinzhou  121000, Liaoning Province, China
  • Received:2010-07-14 Revised:2010-08-28 Online:2011-01-08 Published:2011-01-08
  • About author:Lin Jing-guang, Chief physician, Professor, Second Affiliated Hospital of Liaoning Medical University, Stomatology Hospital of Liaoning Medical University, Jinzhou 121000, Liaoning Province, China 379311389@qq.com; linjg138@sohu.com
  • Supported by:

    the Science and Technology Research Program of Education Department of Liaoning Province, No. 2008339

摘要:

背景:牙周支持组织破坏及附着丧失是导致失牙的最主要原因,细胞因子能促进牙周组织再生形成新附着。
目的:观察血小板衍化生长因子β在人牙周膜成纤维细胞增殖过程中的作用。
方法:体外利用组织块法培养人牙周膜成纤维细胞,对传代后细胞进行组织来源鉴定,通过波丝蛋白、角蛋白免疫组化染色进行定性分析,并加入生物因子血小板衍化生长因子β对人牙周膜成纤维细胞进行增殖诱导,采用MTT法测定吸光度值。
结果与结论:加入质量浓度为10 μg/L的血小板衍化生长因子β后,细胞增殖加速,在加入生长因子血小板衍化生长因子β后,实验组的吸光度显著高于对照组,说明血小板衍化生长因子β对人牙周膜成纤维细胞的增殖具有明显的促进作用。

关键词: 人牙周膜成纤维细胞, 血小板衍化生长因子&beta, 增殖, 慢性牙周炎, 分化

Abstract:

BACKGROUND: Periodontal supporting tissues destroy and attachment losses are the main reasons for tooth loss. Cytokine can promote periodontal tissue regeneration.
OBJECTIVE: To research the effect of platelet-derived growth factor-β (PDGF-β) in the human periodontal ligament cells proliferation.
METHODS: Human fibroblasts were cultured with tissue block method in vitro. The passaged cells were identified by Bosi protein, keratin immunohistochemistry for qualitative analysis. PDGF-β was added to induce periodontal ligament cells proliferation, and the absorbance value was measured by MTT method.
RESULTS AND CONCLUSION: The cell proliferation was accelerated after adding 10 μg/L PDGF-β factor, the absorbance value of the experimental group was greater than that of the control group (P < 0.05). The findings demonstrated that PDGF-β can promote the proliferation of human periodontal ligament cells.

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