机械力会增加牙齿的移动,并促进用牛骨矿物质扩增的牙槽骨缺损的重塑。

IF 4.8 2区 医学 Q1 Dentistry Progress in Orthodontics Pub Date : 2024-01-08 DOI:10.1186/s40510-023-00501-3
Jie Deng, Zi-Meng Zhuang, Xiao Xu, Bing Han, Guang-Ying Song, Tian-Min Xu
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引用次数: 0

摘要

背景:在含有高度和宽度不足的牙槽骨缺损区域进行正畸牙齿移动(OTM)是很难实现的。牛骨矿物质(Bio-Oss)可用于修复牙槽骨缺损;然而,在 OTM 诱导的机械力作用下,用牛骨矿物质移植物(BG)增量的区域是否可用于 OTM,以及巨噬细胞重塑 BG 材料的机制尚不确定:大鼠分为三组:材料和方法:将大鼠分为三组:OTM 组(O)、OTM + BG 材料组(O + B)和对照组(C)。在 O 组和 O + B 组中,拔出第一臼齿以形成骨缺损,并在后者中进行牛骨矿物质移植。两组的第二磨牙均接受 OTM 修复骨缺损。28 天后,使用微聚焦计算机断层扫描(μCT)和扫描电子显微镜(SEM)对上颌骨进行分析,并使用免疫荧光对巨噬细胞(M1/M2)进行染色。在机械力(F)、BG 材料(B)或两者(F + B)条件下培养 THP-1 细胞诱导的巨噬细胞。对吞噬相关信号分子(cAMP/PKA/RAC1)进行分析,并对条件培养基中的 MMP-9 和细胞因子(IL-1β、IL-4)进行分析:结果:我们的研究表明,用 BG 材料移植的牙槽骨缺损可用于 OTM,该区域的 OTM 距离、骨量和骨小梁厚度均显著增加。扫描电镜观察显示,在 OTM 过程中,移植物为细胞迁移和重塑缺损中的 BG 材料提供了支架。此外,M2 巨噬细胞的数量在体内和细胞培养中都明显增加,它们在机械力和 BG 颗粒的作用下通过 cAMP/PKA/RAC1 通路增强了吞噬作用。相比之下,在相同情况下,M1 巨噬细胞数量减少。此外,细胞培养中IL-4水平升高、IL-1β水平降低和MMP-9活性降低也表明M2巨噬细胞极化:本研究探讨了 OTM 期间牛骨矿物质移植物机械力诱导牙槽骨重塑的机制。研究结果可能会为相关的临床问题提供分子见解,如我们是否能将牙齿移入移植材料中,以及这些材料在机械力作用下是如何发生生物重塑和降解的。
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Mechanical force increases tooth movement and promotes remodeling of alveolar bone defects augmented with bovine bone mineral.

Background: Orthodontic tooth movement (OTM) in a region containing alveolar bone defects with insufficient height and width is hard to achieve. Bovine bone mineral (Bio-Oss) is available to restore the alveolar defect; however, whether the region augmented with a bovine bone mineral graft (BG) is feasible for OTM, and the mechanisms by which macrophages remodel the BG material, is uncertain under the mechanical force induced by OTM.

Material and methods: Rats were divided into three groups: OTM (O), OTM + BG material (O + B), and Control (C). First molars were extracted to create bone defects in the O and O + B groups with bovine bone mineral grafting in the latter. Second molars received OTM towards the bone defects in both groups. After 28 days, maxillae were analyzed using microfocus-computed tomography (μCT) and scanning-electron-microscopy (SEM); and macrophages (M1/M2) were stained using immunofluorescence. THP-1 cell-induced macrophages were cultured under mechanical force (F), BG material (B), or both (F + B). Phagocytosis-related signaling molecules (cAMP/PKA/RAC1) were analyzed, and conditioned media was analyzed for MMP-9 and cytokines (IL-1β, IL-4).

Results: Our study demonstrated that alveolar defects grafted with BG materials are feasible for OTM, with significantly increased OTM distance, bone volume, and trabecular thickness in this region. SEM observation revealed that the grafts served as a scaffold for cells to migrate and remodel the BG materials in the defect during OTM. Moreover, the population of M2 macrophages increased markedly both in vivo and in cell culture, with enhanced phagocytosis via the cAMP/PKA/RAC1 pathway in response to mechanical force in combination with BG particles. By contrast, M1 macrophage populations were decreased under the same circumstances. In addition, M2 macrophage polarization was also indicated by elevated IL-4 levels, reduced IL-1β levels, and less active MMP-9 in cell culture.

Conclusion: This study explored the mechanisms of mechanical force-induced alveolar bone remodeling with bovine bone mineral grafts during OTM. The results might provide molecular insights into the related clinical problems of whether we can move teeth into the grafted materials; and how these materials become biologically remodeled and degraded under mechanical force.

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来源期刊
Progress in Orthodontics
Progress in Orthodontics Dentistry-Orthodontics
CiteScore
7.30
自引率
4.20%
发文量
45
审稿时长
13 weeks
期刊介绍: Progress in Orthodontics is a fully open access, international journal owned by the Italian Society of Orthodontics and published under the brand SpringerOpen. The Society is currently covering all publication costs so there are no article processing charges for authors. It is a premier journal of international scope that fosters orthodontic research, including both basic research and development of innovative clinical techniques, with an emphasis on the following areas: • Mechanisms to improve orthodontics • Clinical studies and control animal studies • Orthodontics and genetics, genomics • Temporomandibular joint (TMJ) control clinical trials • Efficacy of orthodontic appliances and animal models • Systematic reviews and meta analyses • Mechanisms to speed orthodontic treatment Progress in Orthodontics will consider for publication only meritorious and original contributions. These may be: • Original articles reporting the findings of clinical trials, clinically relevant basic scientific investigations, or novel therapeutic or diagnostic systems • Review articles on current topics • Articles on novel techniques and clinical tools • Articles of contemporary interest
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