Hosseini Samira, Diegelmann Julia, Folwaczny Matthias, Sabbagh Hisham, Otto Sven, Kakoschke Tamara Katharina, Wichelhaus Andrea, Baumert Uwe, Janjic Rankovic Mila
Department of Orthodontics and Dentofacial Orthopedics, LMU University Hospital, LMU Munich, 80336 Munich, Germany.
Department of Conservative Dentistry and Periodontology, LMU University Hospital, LMU Munich, 80336 Munich, Germany.
Int J Mol Sci. 2024 Dec 17;25(24):13525. doi: 10.3390/ijms252413525.
In recent years, there has been a growing number of adult orthodontic patients with periodontal disease. The progression of periodontal disease is well-linked to oxidative stress (OS). Nevertheless, the impact of OS on orthodontic tooth movement (OTM) is not fully clarified. Therefore, we applied an OS in vitro-model utilizing HO to study its effect on tension-induced mechanotransduction in human osteoblasts (hOBs). Experimental parameters were established based on cell viability and proliferation. Apoptosis detection was based on caspase-3/7 activity. Gene expression related to bone-remodeling (, , /), inflammation (/, , /), autophagy (/, ), and apoptosis (, ) was analyzed by RT-qPCR. IL6 and PGE2 secretion were determined by ELISA. Tension increased the expression of / in all groups, especially after stimulation with higher HO concentration. This corresponds also to the measured PGE2 concentrations. / was upregulated in all groups. Cells subjected to tension alone showed a general upregulation of osteogenic differentiation-related genes; however, pre-stimulation with OS did not induce significant changes especially towards downregulation. /, and were generally upregulated in cells without OS pre-stimulation. Our results suggest that OS might have considerable impacts on cellular behavior during OTM.
近年来,患有牙周病的成年正畸患者数量不断增加。牙周病的进展与氧化应激(OS)密切相关。然而,OS对正畸牙齿移动(OTM)的影响尚未完全阐明。因此,我们应用了一种利用HO的体外OS模型来研究其对人成骨细胞(hOBs)张力诱导的机械转导的影响。基于细胞活力和增殖建立实验参数。凋亡检测基于caspase-3/7活性。通过RT-qPCR分析与骨重塑(、、/)、炎症(/、、/)、自噬(/、)和凋亡(、)相关的基因表达。通过ELISA测定IL6和PGE2分泌。张力增加了所有组中/的表达,尤其是在较高HO浓度刺激后。这也与测得的PGE2浓度相对应。/在所有组中均上调。仅受张力作用的细胞显示成骨分化相关基因普遍上调;然而,用OS预刺激并未诱导显著变化,尤其是下调方面。在没有OS预刺激的细胞中,/、和通常上调。我们的结果表明,OS可能对OTM过程中的细胞行为有相当大的影响。