Zhang Xufang, Chen Qingpiao, Liu Jianwei, Fan Chen, Wei Qi, Chen Zetao, Mao Xueli
1 Guangdong Province Key Laboratory of Stomatology, Department of Operative Dentistry and Endodontics, Guanghua School of Stomatology, Sun Yat-sen University , Guangzhou, People's Republic of China .
2 Institute of Health and Biomedical Innovation, Queensland University of Technology , Brisbane, Australia .
J Interferon Cytokine Res. 2017 Sep;37(9):406-414. doi: 10.1089/jir.2017.0023. Epub 2017 Aug 22.
Periodontitis is a progressive inflammatory disease initiated by bacterial biofilm adhering to the tooth surface. If left untreated, periodontitis may lead to tooth loss and destruction of the alveolar bone. Regaining the lost alveolar bone is a clinical challenge because of the limited differentiation ability of osteoblasts in inflammatory environments. We have previously shown the anti-inflammatory and antiosteoclastogenic activities of parthenolide (PTL) in human periodontal ligament-derived cells by inhibiting nuclear factor kappa B (NF-κB) signaling, indicating its potential for periodontitis treatment. In this study, we further examined whether PTL could stimulate differentiation of osteoblasts from human alveolar bone in inflammatory conditions and investigated the involvement of the Wnt/β-catenin signaling pathway during this process. The results showed that PTL significantly stimulated alkaline phosphatase activity, mineralization nodule formation, and osteogenesis-related gene/protein expression of osteoblasts under the stimulation of tumor necrosis factor-α (TNF-α). In addition, PTL inhibited the NF-κB/p50 pathway and resisted the inhibition of Wnt/β-catenin signaling induced by TNF-α. Our results indicate that the stimulatory effect of PTL on the differentiation of osteoblasts in inflammatory environments may involve the activation of the Wnt/β-catenin signaling pathway, and PTL may be a promising component for bone regeneration in periodontitis treatment.
牙周炎是一种由附着于牙齿表面的细菌生物膜引发的进行性炎症性疾病。如果不进行治疗,牙周炎可能会导致牙齿脱落和牙槽骨破坏。由于成骨细胞在炎症环境中的分化能力有限,恢复丢失的牙槽骨是一项临床挑战。我们之前已经通过抑制核因子κB(NF-κB)信号通路,证明了小白菊内酯(PTL)在人牙周膜来源细胞中的抗炎和抗破骨细胞生成活性,表明其在治疗牙周炎方面的潜力。在本研究中,我们进一步研究了PTL是否能在炎症条件下刺激人牙槽骨成骨细胞的分化,并探讨了Wnt/β-连环蛋白信号通路在此过程中的作用。结果表明,在肿瘤坏死因子-α(TNF-α)刺激下,PTL显著刺激了成骨细胞的碱性磷酸酶活性、矿化结节形成以及成骨相关基因/蛋白表达。此外,PTL抑制了NF-κB/p50通路,并抵抗了TNF-α诱导的Wnt/β-连环蛋白信号通路的抑制。我们的结果表明,PTL在炎症环境中对成骨细胞分化的刺激作用可能涉及Wnt/β-连环蛋白信号通路的激活,并且PTL可能是牙周炎治疗中骨再生的一个有前景的成分。