Department of Orthodontics, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.
Department of Orthodontics, Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran, 1441987566, Tehran, Iran.
Odontology. 2024 Jan;112(1):91-99. doi: 10.1007/s10266-023-00812-1. Epub 2023 May 11.
Periodontal ligament (PDL) cells play an important role in mechanosensing and secretion of signaling molecules during bone remodeling. However, the regulatory mechanism is unknown. The aim of the present study is to investigate the expression pattern of periostin and sclerostin in response to orthodontic forces in periodontal ligament cells in vitro. PDL cells were isolated from extracted teeth and treated with compressive forces of 25 gr/cm or equiaxial tension forces at frequency 1 Hz for 0, 24, 48, and 72 h. qRT-PCR was applied to evaluate the gene expressions. The secretion of sclerostin and periostin was assessed using ELISA. DAPI staining was used to evaluate apoptosis. The expression of sclerostin elevated significantly at protein and gene levels under compression forces after 24 h, while the application of tensile forces induced the expression of periostin and its upstream regulator RUNX2 (p < 0.05). Gene expression up-regulation was significant for POSTN and RUNX2 after 48 and 72 h tensile forces. Also, the gene expression of sclerostin reduced in a time-dependent manner after application of tensile force. The compression forces enhanced apoptosis to 7.5 ± 3.5% and induced gene expression of apoptotic markers of CASP9, and BCL2 within 72 h of exposure. Periostin and sclerostin play an important role in orthodontic loads and their expressions are affected oppositely by compressive and tensile forces that might be suggested as a biomarker for assessment of bone remodeling during orthodontic treatment.
牙周韧带(PDL)细胞在骨重塑过程中的机械感受和信号分子分泌中起重要作用。然而,其调节机制尚不清楚。本研究旨在探讨体外牙周膜细胞中骨桥蛋白和硬骨素在正畸力作用下的表达模式。从拔出的牙齿中分离出牙周膜细胞,用 25gr/cm 的压缩力或 1Hz 的等轴拉伸力处理 0、24、48 和 72h。应用 qRT-PCR 评估基因表达。ELISA 评估硬骨素和骨桥蛋白的分泌。DAPI 染色评估细胞凋亡。在 24h 后,在压缩力下硬骨素的蛋白和基因水平表达显著升高,而拉伸力的应用则诱导了骨桥蛋白及其上游调节因子 RUNX2 的表达(p<0.05)。在 48 和 72h 的拉伸力作用下,POSTN 和 RUNX2 的基因表达也显著上调。此外,在施加拉伸力后,硬骨素的基因表达呈时间依赖性降低。压缩力将细胞凋亡增加到 7.5±3.5%,并在 72h 内诱导了 CASP9 和 BCL2 的凋亡标记物的基因表达。骨桥蛋白和硬骨素在正畸负荷中起重要作用,它们的表达受压缩力和张力的影响相反,这可能被建议作为评估正畸治疗期间骨重塑的生物标志物。