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Journal of Periodontal & Implant Science ; : 273-291, 2017.
Artigo em Inglês | WPRIM | ID: wpr-187091

RESUMO

PURPOSE: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.


Assuntos
Humanos , Fosfatase Alcalina , Western Blotting , Regeneração Óssea , Cálcio , Cemento Dentário , Prótese Dentária , Expressão Gênica , Glicogênio Sintase , Regeneração Tecidual Guiada Periodontal , Imuno-Histoquímica , Proteínas Quinases JNK Ativadas por Mitógeno , Campos Magnéticos , Mineradores , Osteoblastos , Doenças Periodontais , Ligamento Periodontal , Fosforilação , Reação em Cadeia da Polimerase , Proteínas Quinases , Regeneração , Eficiência Biológica Relativa , Transcrição Reversa , RNA Mensageiro , Transdução de Sinais , Proteínas Wnt
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