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体外研究 980nm 半导体激光对人牙周膜细胞在轻力正畸作用下骨改建关键调控因子基因表达的影响

In Vitro Effect of Photobiomodulation Therapy with 980 nm Diode Laser on Gene Expression of Key Regulators of Bone Remodeling by Human Periodontal Ligament Cells under Mild Orthodontic Forces.

机构信息

Department of Orthodontics, School of Dentistry, Tehran University of Medical, Sciences, Tehran, Iran.

Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Photochem Photobiol. 2023 Nov-Dec;99(6):1448-1455. doi: 10.1111/php.13787. Epub 2023 Feb 19.

DOI:10.1111/php.13787
PMID:36718580
Abstract

This study investigated the effect of photobiomodulation (PBM) with 980 nm diode laser as monotherapy and in combination with compressive and tensile orthodontic forces on expression of osteoprotegerin (OPG), receptor activator of nuclear factor-κB ligand (RANKL), sclerostin (SOST) and periostin (POSTN), by human periodontal ligament cells. Isolated cells were cultured and subjected to either tensile (10% elongation) or compressive forces (25 g cm ) for 24 and 48 h. Subsequently, the cells received PBM (100 mW power, 3 or 6 J cm energy density) immediately after load cycle. RT-PCR was applied to assess the genes expression. Data were analyzed by one-way ANOVA, followed by post hoc Tukey test (P ≤ 0.05). We found that PBM in combination with orthodontic forces led to upregulation of bone resorption genes (RANKL and SOST) at the pressure side and their downregulation at the tension side. The expression of osteogenic genes (OPG and POSTN) increased at the tension side and decreased at the pressure side. PBM alone did not affect gene expression. In conclusion, these findings suggest that this PBM protocol may be effective in enhancement of the gene expression in favor of bone remodeling acceleration that should be confirmed in future animal and human studies.

摘要

本研究探讨了 980nm 半导体激光光生物调节(PBM)作为单一疗法以及与压缩和拉伸正畸力联合应用对人牙周膜细胞中核因子-κB 受体激活剂配体(RANKL)、骨保护素(OPG)、硬化蛋白(SOST)和骨膜蛋白(POSTN)表达的影响。分离的细胞进行培养,并分别接受 10%伸长的拉伸力或 25g/cm 的压缩力作用 24 和 48 小时。随后,细胞在负荷循环后立即接受 PBM(100mW 功率,3 或 6J/cm 能量密度)。应用 RT-PCR 评估基因表达。采用单因素方差分析对数据进行分析,然后采用 Tukey 事后检验(P≤0.05)。我们发现,PBM 与正畸力联合作用导致压力侧骨吸收基因(RANKL 和 SOST)上调,张力侧下调。成骨基因(OPG 和 POSTN)在张力侧表达增加,在压力侧表达减少。单独的 PBM 不影响基因表达。综上所述,这些发现表明,这种 PBM 方案可能有助于加速骨重塑,增强有利于骨重塑的基因表达,但这需要在未来的动物和人体研究中进一步证实。

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