Kim Eun-Cheol, Park Jaesuh, Kwon Il Keun, Lee Suk-Won, Park Su-Jung, Ahn Su-Jin
Department of Oral and Maxillofacial Pathology, Institute of Oral Biology, Kyung Hee University School of Dentistry, Seoul, Korea.
Department of Dental Materials, Kyung Hee University School of Dentistry, Seoul, Korea.
J Periodontal Implant Sci. 2017 Oct;47(5):273-291. doi: 10.5051/jpis.2017.47.5.273. Epub 2017 Oct 30.
Although static magnetic fields (SMFs) have been used in dental prostheses and osseointegrated implants, their biological effects on osteoblastic and cementoblastic differentiation in cells involved in periodontal regeneration remain unknown. This study was undertaken to investigate the effects of SMFs (15 mT) on the osteoblastic and cementoblastic differentiation of human osteoblasts, periodontal ligament cells (PDLCs), and cementoblasts, and to explore the possible mechanisms underlying these effects.
Differentiation was evaluated by measuring alkaline phosphatase (ALP) activity, mineralized nodule formation based on Alizarin red staining, calcium content, and the expression of marker mRNAs assessed by reverse transcription polymerase chain reaction (RT-PCR). Signaling pathways were analyzed by western blotting and immunocytochemistry.
The activities of the early marker ALP and the late markers matrix mineralization and calcium content, as well as osteoblast- and cementoblast-specific gene expression in osteoblasts, PDLCs, and cementoblasts were enhanced. SMFs upregulated the expression of Wnt proteins, and increased the phosphorylation of glycogen synthase kinase-3β (GSK-3β) and total β-catenin protein expression. Furthermore, p38 and c-Jun N-terminal kinase (JNK) mitogen-activated protein kinase (MAPK), and nuclear factor-κB (NF-κB) pathways were activated.
SMF treatment enhanced osteoblastic and/or cementoblastic differentiation in osteoblasts, cementoblasts, and PDLCs. These findings provide a molecular basis for the beneficial osteogenic and/or cementogenic effect of SMFs, which could have potential in stimulating bone or cementum formation during bone regeneration and in patients with periodontal disease.
尽管静磁场(SMFs)已用于牙科假体和骨整合植入物,但其对参与牙周再生的细胞中骨细胞和成牙骨质细胞分化的生物学效应仍不清楚。本研究旨在探讨静磁场(15 mT)对人成骨细胞、牙周膜细胞(PDLCs)和成牙骨质细胞的骨细胞和成牙骨质细胞分化的影响,并探索这些效应潜在的机制。
通过测量碱性磷酸酶(ALP)活性、基于茜素红染色的矿化结节形成、钙含量以及通过逆转录聚合酶链反应(RT-PCR)评估的标志物mRNA表达来评估分化。通过蛋白质免疫印迹和免疫细胞化学分析信号通路。
早期标志物ALP的活性以及晚期标志物基质矿化和钙含量,以及成骨细胞、PDLCs和成牙骨质细胞中骨细胞和成牙骨质细胞特异性基因表达均增强。静磁场上调了Wnt蛋白的表达,并增加了糖原合酶激酶-3β(GSK-3β)的磷酸化和总β-连环蛋白的表达。此外,p38和c-Jun氨基末端激酶(JNK)丝裂原活化蛋白激酶(MAPK)以及核因子-κB(NF-κB)通路被激活。
静磁场处理增强了成骨细胞、成牙骨质细胞和PDLCs中的骨细胞和成牙骨质细胞分化。这些发现为静磁场有益的成骨和/或成牙骨质作用提供了分子基础,这可能在骨再生期间刺激骨或牙骨质形成以及在牙周病患者中具有潜力。