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正畸牙齿移动过程中牙周组织中 LIF 和 LIFR 的表达。

Expression of LIF and LIFR in periodontal tissue during orthodontic tooth movement.

机构信息

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST), Hospital and School of Stomatology, Wuhan University, Wuhan, China.

出版信息

Angle Orthod. 2011 Jul;81(4):600-8. doi: 10.2319/102510-622.1. Epub 2011 Mar 25.

DOI:10.2319/102510-622.1
PMID:21446866
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8919751/
Abstract

OBJECTIVES

To test the hypothesis that leukemia inhibitor factor (LIF) and LIF receptor (LIFR) are expressed in periodontal tissue and that their expression may be upregulated during orthodontic tooth movement.

MATERIALS AND METHODS

Forces of 0.3 N were applied to move the upper left first molars mesially in 24 rats. These forces were kept constant for 3, 7, and 14 days and followed by animal sacrifice. The contralateral molars served as control. The rate of tooth movement was measured by Image J software. Paraffin-embedded sections of the upper jaws were prepared for histological and immunohistochemical analysis to test the LIF and LIFR expression.

RESULTS

Loaded teeth showed a significantly higher rate of tooth movement. The periodontium of the moved teeth experienced tissue remodeling, while there was no obvious change in the contralateral controls. Furthermore, LIF and LIFR were expressed in the periodontal tissue, and there were statistically significant differences between the loaded and unloaded teeth at 3 and 14 days. LIF presented significantly higher expression on the tension side compared with the pressure side at 3 days.

CONCLUSION

Both LIF and LIFR exist in the periodontal tissue, and continuous orthodontic forces induce the upregulation of LIF/LIFR production, suggesting that LIF/LIFR may play important roles in periodontium remodeling.

摘要

目的

验证成纤维细胞生长因子 9(LIF)及其受体(LIFR)在牙周组织中表达,以及在正畸牙移动过程中其表达可能上调的假说。

材料与方法

将 24 只大鼠左侧上颌第一磨牙向近中施以 0.3N 的力。这些力持续 3、7 和 14 天,然后处死动物。对侧磨牙作为对照。通过 Image J 软件测量牙齿移动速度。制备上颚石蜡包埋切片进行组织学和免疫组织化学分析,以检测 LIF 和 LIFR 的表达。

结果

负载牙齿的牙齿移动速度明显更高。移动牙齿的牙周组织经历了组织重塑,而对侧对照牙齿没有明显变化。此外,LIF 和 LIFR 存在于牙周组织中,在加载和未加载牙齿之间在 3 天和 14 天时有统计学差异。在 3 天时,LIF 在张应力侧的表达明显高于压应力侧。

结论

LIF 和 LIFR 均存在于牙周组织中,持续的正畸力诱导 LIF/LIFR 的产生上调,提示 LIF/LIFR 可能在牙周组织重塑中发挥重要作用。

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本文引用的文献

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On a path to unfolding the biological mechanisms of orthodontic tooth movement.在探索正畸牙齿移动生物学机制的道路上。
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Immunolocalization of CSF-1, RANKL and OPG in the enamel-related periodontium of the rat incisor and their implications for alveolar bone remodeling.在大鼠切牙牙釉质相关牙周组织中 CSF-1、RANKL 和 OPG 的免疫定位及其对牙槽骨重塑的意义。
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IL-1beta and TNF-alpha regulate IL-6-type cytokines in gingival fibroblasts.白细胞介素-1β和肿瘤坏死因子-α调节牙龈成纤维细胞中的白细胞介素-6型细胞因子。
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Differential expression of osteoblast and osteoclast chemmoatractants in compression and tension sides during orthodontic movement.正畸移动过程中压缩侧和拉伸侧成骨细胞与破骨细胞趋化因子的差异表达
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Cytokine expression pattern in compression and tension sides of the periodontal ligament during orthodontic tooth movement in humans.人类正畸牙齿移动过程中牙周膜受压侧和受拉侧的细胞因子表达模式
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LIF inhibits osteoblast differentiation at least in part by regulation of HAS2 and its product hyaluronan.白血病抑制因子(LIF)至少部分地通过调节透明质酸合酶2(HAS2)及其产物透明质酸来抑制成骨细胞分化。
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Interleukin-1alpha and tumor necrosis factor-alpha expression during the early phases of orthodontic tooth movement in rats.白细胞介素-1α和肿瘤坏死因子-α在大鼠正畸牙移动早期阶段的表达
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