The 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.
Orthodontic Department Division II, School & Hospital of Stomatology, Wuhan University, Wuhan, China.
J Periodontal Res. 2023 Oct;58(5):907-918. doi: 10.1111/jre.13143. Epub 2023 Jun 21.
To verify the role of YAP/WNT5A/FZD4 axis in stretch-induced osteogenic differentiation of hPDLCs.
During orthodontic tooth movement, differentiation of human periodontal ligament cells (hPDLCs) at the tension side of the periodontal ligament mediates new bone formation. WNT5A promotes osteogenesis and its regulator Yes-associated protein (YAP) is responsive to mechanical stimulation in hPDLCs. However, the mechanisms of YAP and WNT5A in alveolar bone remodeling remain unclear.
Cyclic stretch was applied to hPDLCs to mimic the orthodontic stretching force. Osteogenic differentiation was determined by alkaline phosphatase (ALP) activity, Alizarin Red staining, qRT-PCR and western blotting. To detect activation of YAP and expression of WNT5A and its receptor Frizzled-4 (FZD4), western blotting, immunofluorescence, qRT-PCR and ELISA were performed. Verteporfin, Lats-IN-1, small interfering RNAs and recombinant protein were used to explore the relationship of YAP, WNT5A and FZD4, and the effect of their relationship on stretch-induced osteogenesis of hPDLCs.
WNT5A, FZD4 and nuclear localization of YAP were upregulated by cyclic stretch. YAP positively regulated WNT5A and FZD4 expression and osteogenic differentiation of hPDLCs under cyclic stretch by YAP inhibition or activation assay. Knockdown of WNT5A and FZD4 attenuated YAP-induced and stretch-induced osteogenic differentiation. Recombinant WNT5A rescued the suppressed osteogenic differentiation by YAP inhibitor in hPDLCs, whereas knockdown of FZD4 weakened the effect of WNT5A and amplified the suppression.
WNT5A/FZD4 could be positively regulated by YAP and the YAP/WNT5A/FZD4 axis mediated osteogenic differentiation of hPDLCs under cyclic stretch. This study provided further insight into the biological mechanism of orthodontic tooth movement.
验证 YAP/WNT5A/FZD4 轴在牵张诱导 hPDLC 成骨分化中的作用。
在正畸牙齿移动过程中,牙周膜细胞(hPDLCs)在牙周膜的张力侧的分化介导新骨形成。WNT5A 促进成骨,其调节因子 Yes 相关蛋白(YAP)对 hPDLCs 的机械刺激有反应。然而,YAP 和 WNT5A 在牙槽骨重塑中的机制尚不清楚。
应用循环拉伸模拟正畸拉伸力,以 hPDLCs 为模型。通过碱性磷酸酶(ALP)活性、茜素红染色、qRT-PCR 和 Western blot 检测成骨分化。Western blot、免疫荧光、qRT-PCR 和 ELISA 检测 YAP 激活和 WNT5A 及其受体 Frizzled-4(FZD4)的表达。使用 Verteporfin、Lats-IN-1、小干扰 RNA 和重组蛋白来探讨 YAP、WNT5A 和 FZD4 之间的关系,以及它们之间的关系对 hPDLCs 牵张诱导成骨的影响。
循环拉伸可上调 WNT5A、FZD4 和 YAP 的核定位。通过 YAP 抑制或激活实验,YAP 正向调节 WNT5A 和 FZD4 的表达以及循环拉伸下 hPDLCs 的成骨分化。WNT5A 和 FZD4 的敲低减弱了 YAP 诱导和牵张诱导的成骨分化。重组 WNT5A 挽救了 YAP 抑制剂对 hPDLCs 成骨分化的抑制作用,而 FZD4 的敲低减弱了 WNT5A 的作用并放大了抑制作用。
在循环拉伸下,WNT5A/FZD4 可被 YAP 正向调节,YAP/WNT5A/FZD4 轴介导 hPDLCs 的成骨分化。本研究为正畸牙齿移动的生物学机制提供了进一步的认识。