期刊导航

论文摘要

正畸力作用下兔牙周组织中雷帕霉素靶蛋白和核糖体蛋白S6激酶的表达

Expression of mammalian target of rapamycin and p70 S6 kinase in rabbit periodontal tissues remodeling uring orthodontic tooth movement

作者:刘奕 郭亚峰

Author:LIU Yi1, GUO Ya-feng2

收稿日期:2008-12-25          年卷(期)页码:2008,26(06):580-

期刊名称:华西口腔医学杂志

Journal Name:West China Journal of Stomatology

关键字:正畸力,雷帕霉素靶蛋白,核糖体蛋白S6激酶,牙周组织改建,

Key words:orthodontics,mammaliantargetofrapamycin,p70S6kinase,periodontiumremodeling,

基金项目:

沈阳市科学技术计划基金资助项目(1072033-1-00)

中文摘要

目的探讨正畸牙移动过程中雷帕霉素靶蛋白(mTOR)和核糖体蛋白S6激酶(p70 S6K)在牙周组织改建中的作用。方法选用24只日本大耳白兔建立正畸牙移动的动物模型,将实验动物上颌右侧戴矫治器,作为实验侧;左侧未戴矫治器,作为对照侧。分别在戴矫治器后3、5、7、14 d各处死6只实验动物。采用苏木精-伊红染色、逆转录聚合酶链反应(RT-PCR)及Western blot免疫印迹分析方法观察牙周组织形态学变化及mTOR和p70 S6K表达的变化。结果组织形态学观察可见,实验侧牙周组织较对照侧有明显改建,牙槽骨由致密变得疏松,细胞的排列由有序变得紊乱,牙槽骨的骨壁由平整变得凹凸不平,出现了破骨细胞及骨陷窝。RT-PCR结果显示,加力3 d后牙周组织中p70 S6K mRNA表达增强,7 d后牙周组织中p70 S6K mRNA明显增强,随后缓慢下降,与对照侧相比,其差异有统计学意义(P<0.01)。Western blot免疫印迹分析与RT-PCR结果一致。结论在正畸牙移动过程中,兔牙周组织中mTOR和p70 S6K的表达明显增强,提示mTOR和p70 S6K参与牙周组织改建,并在牙周组织改建中起重要作用。

英文摘要

Objective To study the role of mammalian target of rapamycin(mTOR) and p70 S6 kinase(p70 S6K) in periodontal tissues remodeling during orthodontic tooth movement. Methods Twenty -four rabbits were chosen to establish rabbit models for the study. The right maxillary teeth of each animal treated by orthodontics were the test sides, and the untreated left teeth were the control sides. The animals were sacrificed at 3, 5, 7, 14 d, espectively. The prepared tissue specimens were processed for the study of the change in the histologic morphology ith HE staining and the expression of p70 S6K in periodontal tissues by reverse transcription-polymerase chain eaction(RT-PCR) and Western blot techniques. Results In the test side, the tranecula of bone became porous nd cells arrayed disorderly, resorption of alveolar bone was observed in histological study. There were many holes n the alveolar bone, osteoblasts were occasionally observed. RT-PCR showed that the expression of p70 S6K mRNA ramatically changed at 3 d. The expression of p70 S6K mRNA in treating periodontal tissues was higher than the ontrol side, especially at 7 d, and then decreased. Compared with the control side, there was significant difference n statistical analysis(P <0.01). The expression of Western blot was same as the RT -PCR. Conclusion Higher xpression of mTOR and p70 S6K during orthodontic tooth movement especially plays an important role in the process f periodontium remodeling.

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