Yu Hang, Wei Xiaoxi, Jiang Huan, Qi Huichuan, Zhang Yi, Hu Min
Department of Orthodontics, Stomatology School of Jilin University, No. 1500 Qinghua Road, ChaoYang Area, Changchun City, Jilin Province, P.R. China.
Jilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, School and Hospital of Stomatology, Jilin University, Changchun City, Jilin Province, P.R. China.
BMC Oral Health. 2025 Jan 22;25(1):118. doi: 10.1186/s12903-025-05491-8.
To investigating whether osteogenic differentiation of osteoblasts promoted by tension force (TF) is mediated by ephrinB2-EphB4 signaling.
TF was applied to MC3T3-E1 cells, then CCK-8 and live/dead staining were used to detect cell proliferation. Levels of osteogenic differentiation-related factors were detected by ALP staining, ARS staining, qPCR and western blot. NVP-BHG712 was used to block EphB4 receptor. Establishing a rat orthodontic tooth movement (OTM) model, ephrinB2-Fc and NVP-BHG712 were used to treat rats. Micro-CT and H&E staining were used to detect alveolar bone. Changes of MAPK pathways were detected to investigate whether they were downstream of ephrinB2-EphB4 signaling in mediating TF promote osteogenic differentiation.
We explored the effect of TF on MC3T3-E1 cells, and found that TF significantly promoted osteogenic differentiation, but when EphB4 receptor was blocked, the promotion was inhibited. In vivo, we found that TF improved alveolar bone formation through ephrinB2-EphB4 signaling. Further investigation into the signaling pathways revealed that TF significantly increased levels of MAPK pathways, however, when EphB4 receptor was blocked, only the promotion of p-ERK1/2 was decreased.
TF promotes osteogenic differentiation through ephrinB2-EphB4 signaling and ERK1/2 pathway is a downstream of ephrinB2-EphB4 signaling partially mediate mediates TF-induced promotion of osteogenic differentiation.
研究牵张力(TF)促进成骨细胞成骨分化是否由ephrinB2-EphB4信号介导。
对MC3T3-E1细胞施加TF,然后用CCK-8和活/死染色检测细胞增殖。通过碱性磷酸酶(ALP)染色、茜素红染色(ARS染色)、定量聚合酶链反应(qPCR)和蛋白质免疫印迹法检测成骨分化相关因子水平。使用NVP-BHG712阻断EphB4受体。建立大鼠正畸牙移动(OTM)模型,用ephrinB2-Fc和NVP-BHG712处理大鼠。用显微计算机断层扫描(Micro-CT)和苏木精-伊红染色(H&E染色)检测牙槽骨。检测丝裂原活化蛋白激酶(MAPK)通路的变化,以研究其是否为ephrinB2-EphB4信号下游,介导TF促进成骨分化。
我们探讨了TF对MC3T3-E1细胞的影响,发现TF显著促进成骨分化,但当EphB4受体被阻断时,这种促进作用受到抑制。在体内,我们发现TF通过ephrinB2-EphB4信号改善牙槽骨形成。对信号通路的进一步研究表明,TF显著提高了MAPK通路的水平,然而,当EphB4受体被阻断时,只有p-ERK1/2的促进作用降低。
TF通过ephrinB2-EphB4信号促进成骨分化,ERK1/2通路是ephrinB2-EphB4信号的下游,部分介导TF诱导的成骨分化促进作用。