Department of Plastic and Reconstructive Surgery, Dongguk University Medical Center, Goyang-si 10326, Korea.
Department of Medical Biotechnology, Dongguk University, Goyang-si 10326, Korea.
Int J Mol Sci. 2021 Sep 21;22(18):10167. doi: 10.3390/ijms221810167.
Mechanical/physical stimulations modulate tissue metabolism, and this process involves multiple cellular mechanisms, including the secretion of growth factors and the activation of mechano-physically sensitive kinases. Cells and tissue can be modulated through specific vibration-induced changes in cell activity, which depend on the vibration frequency and occur via differential gene expression. However, there are few reports about the effects of medium-magnitude (1.12 g) sonic vibration on the osteogenic differentiation of human dental pulp stem cells (HDPSCs). In this study, we investigated whether medium-magnitude (1.12 g) sonic vibration with a frequency of 30, 45, or 100 Hz could affect the osteogenic differentiation of HDPSCs. Their cell morphology changed to a cuboidal shape at 45 Hz and 100 Hz, but the cells in the other groups were elongated. FACS analysis showed decreased CD 73, CD 90, and CD 105 expression at 45 Hz and 100 Hz. Additionally, the proportions of cells in the G0/G1 phase in the control, 30 Hz, 45 Hz, and 100 Hz groups after vibration were 60.7%, 65.9%, 68.3%, and 66.7%, respectively. The mRNA levels of osteogenic-specific markers, including osteonectin, osteocalcin, BMP-2, ALP, and Runx-2, increased at 45 and 100 Hz, and the ALP and calcium content was elevated in the vibration groups compared with those in the control. Additionally, the western blotting results showed that p-ERK, BSP, osteoprotegerin, and osteonectin proteins were upregulated at 45 Hz compared with the other groups. The vibration groups showed higher ALP and calcium content than the control. Vibration, especially at 100 Hz, increased the number of calcified nodes relative to the control group, as evidenced by von Kossa staining. Immunohistochemical staining demonstrated that type I and III collagen, osteonectin, and osteopontin were upregulated at 45 Hz and 100 Hz. These results suggest that medium magnitude vibration at 45 Hz induces the G0/G1 arrest of HDPSCs through the p-ERK/Runx-2 pathway and can serve as a potent stimulator of differentiation and extracellular matrix production.
机械/物理刺激调节组织代谢,这个过程涉及多种细胞机制,包括生长因子的分泌和机械敏感激酶的激活。细胞和组织可以通过特定的振动诱导的细胞活性变化来调节,这取决于振动频率,并通过差异基因表达发生。然而,关于中强度(1.12g)声波振动对人牙髓干细胞(HDPSCs)成骨分化的影响的报道很少。在这项研究中,我们研究了中强度(1.12g)的声波振动频率为 30、45 或 100Hz 是否会影响 HDPSCs 的成骨分化。它们的细胞形态在 45Hz 和 100Hz 时变为立方形状,但其他组的细胞则拉长。FACS 分析显示,在 45Hz 和 100Hz 时,CD73、CD90 和 CD105 的表达降低。此外,在振动后对照组、30Hz、45Hz 和 100Hz 组中细胞处于 G0/G1 期的比例分别为 60.7%、65.9%、68.3%和 66.7%。骨形成特异性标志物,包括骨桥蛋白、骨钙素、BMP-2、ALP 和 Runx-2 的 mRNA 水平在 45Hz 和 100Hz 时增加,振动组的 ALP 和钙含量高于对照组。此外,Western blotting 结果显示,与其他组相比,p-ERK、BSP、骨保护素和骨桥蛋白蛋白在 45Hz 时上调。振动组的 ALP 和钙含量高于对照组。与对照组相比,振动,尤其是 100Hz,增加了矿化节点的数量,这一点可以通过 von Kossa 染色证明。免疫组织化学染色显示,I 型和 III 型胶原蛋白、骨桥蛋白和骨钙素在 45Hz 和 100Hz 时上调。这些结果表明,45Hz 的中等强度振动通过 p-ERK/Runx-2 途径诱导 HDPSC 的 G0/G1 期阻滞,并可作为分化和细胞外基质产生的有效刺激物。