期刊文献+

大鼠正畸牙移动过程中压力侧牙周组织NALP3的表达 被引量:3

NALP3 expression in periodontal tissues of pressure side during orthodontic tooth movement in rats
下载PDF
导出
摘要 目的观察大鼠正畸牙移动过程中压力侧牙周组织NALP3的表达,探讨NALP3在正畸牙移动过程中的作用。方法将50只6周龄雄性SD大鼠随机分为10组,每组5只。以左上第一磨牙作为实验牙,分别加力0、1、3、6、12h、1、3、7、14、21d。制备不同时间牙周组织切片,进行HE染色和NALP3免疫组化染色。结果正畸牙移动过程中压力侧牙周组织NALP3的表达发生变化。加力后牙周膜NALP3表达即增加,3h达到小高峰,随后降低,1d后表达再次增加,7d后达到最高峰。结论 NALP3参与了正畸牙移动过程中牙周组织的改建。 Objective To examine the NALP3 expression in periodontal tissues of pressure side during orthodontic tooth movement in rats, and to explore the role of NALP3 during orthodontic tooth movement. Methods Fifty male SD rats aged 6 weeks old were randomly divided into 10 groups of 5. The upper left first molar was experimental tooth, which was pulled mesially by orthodontic force for 0, 1, 3, 6, 12 hours, 1, 3, 7, 14, 21 days respectively. Routine five-micrometer paraffin tissue sections were prepared and HE staining and immunohistochemical staining for NALP3 were carried out. Results The expression of NALP3 increased in pressure zone of periodontal ligament after loading, reaching a peak on the third hour and then decreased. The NALP3 expression increased again after one day, and reached the peak on the seventh day. Conclusion NALP3 was involved in the process of periodontal tissue remodeling during orthodontic tooth movement in rats.
作者 何正权 杨凯
出处 《北京口腔医学》 CAS 2014年第3期129-132,共4页 Beijing Journal of Stomatology
基金 北京市教委科技计划面上项目(KM201310025021) 北京市自然科学基金(7133242)
关键词 正畸 牙齿移动 NALP3 牙周组织改建 Orthodontics Tooth movement NALP3 Periodontal tissue remodeling
  • 相关文献

参考文献10

  • 1杨美祥,丁寅,徐如生,邹邦新.正畸牙齿移动中IL-1β在骨质疏松大鼠牙周组织中的分布变化[J].华西口腔医学杂志,2000,18(5):314-316. 被引量:9
  • 2张立智,蒋垚.骨免疫学研究进展[J].国际骨科学杂志,2009,30(4):218-220. 被引量:14
  • 3Fantuzzi G, Dinarello CA. Interleukin-18 and interleukin-1 beta : two cytokine substrates for ICE ( caspase-1 ). J Clin Immunol, 1999,19 (1):1-11.
  • 4Dinarello CA. Interleukin-1 beta, interleukin-18, and theinterleukin- 1 beta converting enzyme. Ann N Y Acad Sci, 1998,856 (1) :1-11.
  • 5Martinon F , Tschopp J. Inflammatory caspases and inflammasomes:master switches of inflammation. Cell Death Differ, 2007,14 ( 1 ) : 10- 22.
  • 6Schroder K, Tschopp J. The inflammasomes. Cell, 2010, 140 ( 6 ) : 821- 832.
  • 7Mayor A,Martinon F, De Smedt T,et al. A crucial function of SC, T1 and HSP90 in inflammasome activity links mammalian andplant innate immune responses. Nat lmmunol,2007,8 (5) :497-503.
  • 8Giamarellos-Bourboulis E J, Mouktaroudi M, Bodar E, et al. Crystals of monosodiurn urate monohydrate enhance lipopolysaccharide- induced release of interleukin 1 beta by mononuclear cells through a easpase 1-mediated process. Ann Rheum Dis ,2009,68 (2) :273-278.
  • 9Beck C, Morbaeh H, Riehl P, et al. How can calcium pyrophosphate crystals induce inflammation in hypophosphatasia or chronic inflammatory joint diseases.'? Rheumatol Int ,2008,29 (3) :229-238.
  • 10Bostanci N, Emingil G, Saygan B, et al. Expression and regulation of the NALP3 inflammasome complex in periodontal diseases. Clini Exp Immunol.2009. 157(3) ,415-422.

二级参考文献3

共引文献21

同被引文献26

引证文献3

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部