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小鼠正畸牙齿移动过程中的骨细胞死亡

Osteocyte death during orthodontic tooth movement in mice.

作者信息

Moin Sogole, Kalajzic Zana, Utreja Achint, Nihara Jun, Wadhwa Sunil, Uribe Flavio, Nanda Ravindra

机构信息

a  Private Practice, Clinician, Manchester, NH.

出版信息

Angle Orthod. 2014 Nov;84(6):1086-92. doi: 10.2319/110713-813.1. Epub 2014 Apr 2.

Abstract

OBJECTIVE

To investigate the time course of osteocyte death in a mouse model of orthodontic tooth movement (OTM) and its association to the caspase-3 activation pathway and osteoclast formation.

MATERIALS AND METHODS

Twenty-five male wild type CD-1 mice (8-12 weeks old) were loaded with an orthodontic appliance. A spring delivering 10-12 g of force was placed between the right first molar and the incisor to displace the first molar mesially. The contralateral unloaded sides served as the control. The animals were equally divided into five different time points: 6, 12, 24, and 72 hours and 7 days of orthodontic loading. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay, caspase-3 immunostaining, and tartrate-resistant acid phosphatase (TRAP) staining was performed on histologic sections of the first molars. The labeling was quantified in osteocytes on the compression side of the alveolar bone at each time point.

RESULTS

TUNEL labeling significantly increased at 12, 24, and 72 hours after orthodontic loading; the peak was observed at 24 hours. Elevated caspase-3 labeling was noted at 12, 24, and 72 hours and 7 days after loading, although the increase was not significant. Significant osteoclast formation was initially evident after 72 hours and progressively increased up to 7 days.

CONCLUSIONS

Osteocyte death during OTM peaks at 24 hours, earlier than initial osteoclast activation. However, only a slight trend for increased caspase-3 activity suggests that other mechanisms might be involved in osteocyte death during OTM.

摘要

目的

研究正畸牙移动(OTM)小鼠模型中骨细胞死亡的时间进程及其与半胱天冬酶-3激活途径和破骨细胞形成的关系。

材料与方法

25只8-12周龄雄性野生型CD-1小鼠佩戴正畸矫治器。在右侧第一磨牙和切牙之间放置一个施加10-12克力的弹簧,使第一磨牙向近中移动。对侧未加载的一侧作为对照。将动物平均分为五个不同的时间点:正畸加载后6、12、24、72小时和7天。对第一磨牙的组织切片进行末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)检测、半胱天冬酶-3免疫染色和抗酒石酸酸性磷酸酶(TRAP)染色。在每个时间点对牙槽骨受压侧的骨细胞中的标记进行定量分析。

结果

正畸加载后12、24和72小时TUNEL标记显著增加;在24小时观察到峰值。加载后12、24、72小时和7天半胱天冬酶-3标记升高,尽管增加不显著。72小时后破骨细胞形成最初明显,并持续增加直至7天。

结论

OTM期间骨细胞死亡在24小时达到峰值,早于初始破骨细胞激活。然而,半胱天冬酶-3活性仅略有增加的趋势表明,OTM期间骨细胞死亡可能涉及其他机制。

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