State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, School & Hospital of Stomatology, Wuhan University, Wuhan, China.
State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, School & Hospital of Stomatology, Wuhan University, Wuhan, China.
Int J Biochem Cell Biol. 2020 Dec;129:105862. doi: 10.1016/j.biocel.2020.105862. Epub 2020 Oct 10.
During the orthodontic tooth movement, cells in periodontal ligament could differentiate into osteoblasts to synthesize alveolar bone as well as affect the proliferation, migration and differentiation of mesenchymal stem cells, which also contribute to bone remodeling. However, the mechanism is still largely elusive. Here, we evaluated the expression of CREB at the tension site of mouse periodontal ligament under orthodontic mechanical strain and in the cyclic tension strain treated human periodontal ligament cells. Then, through gain and loss of function analysis, we revealed that CREB in PDLCs promotes SDF-1 and FGF2 secretion, which enhance the migration and osteoblastic differentiation of BMSCs. We further discovered that CREB transcriptionally activates FGF2 and SDF-1 expressions by binding to the promoter regions.In conclusion, this study confirms that CREB is an upregulated gene in periodontal ligament under orthodontic tension strain stimulation and plays an important role in regulating BMSCs' physiological activity in orthodontic tension strain-induced bone formation.
在正畸牙齿移动过程中,牙周膜中的细胞可分化为成骨细胞,合成牙槽骨,并影响间充质干细胞的增殖、迁移和分化,从而促进骨重塑。然而,其机制在很大程度上仍不清楚。在这里,我们评估了在正畸机械应变下和在周期性张力应变处理的人牙周膜细胞中,小鼠牙周膜张力部位的 CREB 的表达。然后,通过功能获得和丧失分析,我们揭示了 PDLCs 中的 CREB 促进 SDF-1 和 FGF2 的分泌,从而增强 BMSCs 的迁移和成骨分化。我们进一步发现,CREB 通过结合启动子区域转录激活 FGF2 和 SDF-1 的表达。总之,本研究证实,在正畸张力应变刺激下,牙周膜中的 CREB 是一个上调基因,在调节 BMSCs 在正畸张力应变诱导的骨形成中的生理活性方面发挥重要作用。