《口腔颌面外科杂志》 ›› 2012, Vol. 22 ›› Issue (5): 328-332. doi: 10.3969/j.issn.1005-4979.2012.05.005

• 基础研究 • 上一篇    下一篇

干细胞因子在大鼠下颌骨缺损修复中的表达研究

徐丽, 朱思姮, 邹多宏, 窦晓晨, 周健   

  1. 安徽医科大学口腔医学院·附属口腔医院颌面外科,安徽省口腔临床医学重点学科,安徽省口腔疾病研究省级实验室,中央与地方共建口腔医学中心实验室,安徽  合肥  230032
  • 出版日期:2012-10-28 发布日期:2013-01-02
  • 通讯作者: 周健,教授. E-mail: zj@ahmu. edu. cn
  • 作者简介:徐丽(1987—),女,安徽合肥人,硕士研究生. E-mail: kqxuli@163.com
  • 基金资助:

    国家自然科学基金资助项目( 81100788,81070864);安徽医科大学博士科研启动基金项目 (XJ201109);安徽医科大学科研基金项目(2011xkj017)

Expression of Stem Cell Factor during the Process of Regeneration in Bone Defect of Mandibule

XU Li, ZHU Si-heng, ZOU Duo-hong, DOU Xiao-chen, ZHOU Jian   

  1. Department of Oral and Maxillofacial Surgery, School and Hospital of Stomatology, Anhui Medical University, Key Subject of Oral Clinical Medicine of Anhui Province, Provincial-Level Lab of Oral Disease Research of Anhui Province, Stomatology Central Lab Built Together by Central and Local Government, Hefei 230032, Anhui Province, China
  • Online:2012-10-28 Published:2013-01-02

摘要: 目的: 探讨在SD大鼠下颌骨临界性骨缺损(critical size bone defect,CSD)与自愈性骨缺损修复过程中,各时相点干细胞因子(stem cell factor, SCF)的表达情况。方法: ①分别在36只SD大鼠双侧下颌骨的下颌角部制造临界性骨缺损(直径5 mm)和自愈性骨缺损(直径2 mm)模型,实验动物分为6组,在术后第1、3、5、7、14、21天分别处死;②利用免疫组织化学方法检测骨缺损区各时相点SCF的表达情况;③利用Western印迹法检测骨缺损区各时相点SCF存在与否,并进行半定量分析。结果: 成功构建了大鼠双侧下颌骨的临界性骨缺损和自愈性骨缺损模型。免疫组织化学结果显示,骨缺损愈合的各时相点SCF均有较高的表达,但SCF在临界性骨缺损组各时相点的表达,均低于自愈性骨缺损组。结论: SCF在骨缺损修复中发挥重要的作用。

关键词:  , 干细胞生长因子, 临界性骨缺损, 自愈性骨缺损,

Abstract: Objective: The current paper was aimed to detect the expression of stem cell factor (SCF) during the repair process of rats′ mandibular defects.  Methods: 36 SD rats were used in this study. In one side of the mandible , critical size bone defect (CSD) in 5 mm dimension was established. A self-healing bone defect in 2 mm dimension was created in the contralateral side of the mandible. Animals were randomly divided into 6 groups and sacrificed on 1, 3, 5, 7, 14, 21 d after surgery respectively. Expression of SCF during the regeneration process were determined by immunohistochemistry and Western blot. Data were expressed as x+s by SPSS 13.0 software. We used Student′s t test to determine the significance of difference between groups.  Significance was set at P<0.05. Results: The expression of SCF genes was detected in both groups at all times, and expression of SCF in CSD group was weaker  than those in self-healing bone defect group at the same time(P<0.05). The results of western blot also confirmed the results by immunohistochemistry. Conclusion: SCF plays an important role in bone defect repair.

Key words: stem cell factor, critical size defect, self-healing size defect, rat

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