RESUMO
Objective:To study the effects of recombinant human platelet-derived growth factor-BB(rhPDGF-BB)combined with recombinant human transforming growth factor-β1 (rhTGF-β1 )on the expression of FAK mRNA of osteoclasts in the alveolar bone on the pressure side of orthodontic teeth in rats.Methods:Orthodontic tooth movement model was established in 160 male SD rats.The rats in experimental group were treated by injection of 10 ng rhPDGF-BB and 5 ng rhTGF-β1 in the buccal submucosal area of the mo-lar every other day from day 1 afterburner,while those in control group received equivalent volumes of PBS.The rats were sacrificed at 1,4,7,10 and 14 days(n=16)after appliance placement.Specimens were collected.Osteoclasts in the alveolar bone on the pres-sure side of the orthodontic teeth were observed by TRAP staining,the FAK mRNA expression was quantified by quantitative RT-PCR.Results:rhPDGF-BB combined with rhTGF-β1 significantly promoted an increasing number of osteoclasts on the compressing side(P0.05) at day 14.Conclusion:Combination of rhPDGF-BB and rhTGF-β1 can increase the number of osteoclasts in the alveolar bone on compressing side,and promote FAK mRNA expression in osteoclasts.
RESUMO
PURPOSE: This study was to investigate the effects of recombinant human platelet-derived growth factor (rhPDGF-BB) and heparin to titanium surfaces for enhancement of osteoblastic functions and inhibition of inflammation activity. MATERIALS AND METHODS: The anodized titanium discs, not coated with any material, were used as a control group. In heparinized- Ti group, dopamine was anchored to the surface of Ti substrates, and coated with heparin. In PDGF-Ti group, rhPDGF-BB was immobilized onto heparinized Ti surface. The surface morphologies were investigated by the scanning electron microscope in each group. The release kinetics of rhPDGF-BB were analyzed, and cytotoxicity tests for each group were conducted. The biocompatibilities were characterized by measuring cell proliferation, alkaline phosphatase activity, and calcium deposition using MG-63 cells. Statistical comparisons were carried out by one-way ANOVA tests. Differences were considered statistically significant at *P<.05 and **P<.001. RESULTS: The combination of rhPDGF-BB and heparin stimulated alkaline phosphatase activity and OCN mRNA expression in osteoblastic cells (*P<.05 and **P<.001). MG-63 cells grown on PDGF-Ti had significantly higher amounts of calcium deposition than those grown on anodized Ti (**P<.001). Heparinized Ti was more anti-inflammatory compared to anodized Ti, when exposed to lipopolysaccharide using the transcript levels of TNF-alpha and IL-6 of proinflammatory cytokine (*P<.05 and **P<.001). CONCLUSION: The result of this study demonstrated that the incorporation of rhPDGF-BB and heparin onto Ti surface enhanced osteoblastic functions and inhibited inflammation.
Assuntos
Humanos , Fosfatase Alcalina , Cálcio , Proliferação de Células , Dopamina , Elétrons , Heparina , Imobilização , Inflamação , Interleucina-6 , Cinética , Osteoblastos , Fator de Crescimento Derivado de Plaquetas , Proteínas Proto-Oncogênicas c-sis , RNA Mensageiro , Titânio , Fator de Necrose Tumoral alfaRESUMO
OBJECTIVE: The present study is aimed to test minimum threshold rhPDGF-BB concentration required to obtain greater root surface biocompatibility and most suitable condition for fibroblast cell attachment and growth in chronic periodontitis. MATERIAL AND METHOD: Proximal surfaces of twenty selected periodontitis teeth were prepared and divided into four groups (ten specimens/each): - I: untreated diseased (control); II: scaling & root planning (SRP); III: SRP then rhPDGF-BB application (50ng/ml); IV: SRP then rhPDGF-BB application (25ng/ml). Fibroblasts were pooled on root specimens, then specimens were incubated. Results of both cell count and shape were assessed by SEM and evaluated repeatedly within a representative standard area. RESULTS: Group II: showed a comparable negative effect, since no significant differences found.Group III: showed a significant positive effect, higher than both groups I & II but lower than group IV. Group IV: demonstrated the best results for cell quantity & quality, where it had favorable significant differences when compared to all others. CONCLUSION: rhPDGF-BB with 25ng/ml concentration showed a more positive effect in getting higher fibroblast cell count & more healthy cell shape than rhPDGF-BB (50ng/ml). A promising role of rhPDGF-BB (25ng/ml) as good modulating agent for fibroblast cell attachment in chronic periodontitis may be suggested.
OBJETIVO: O presente estudo objetivou testar o limite de concentração rhPDGF-BB requerido para obter maior biocompatibilidade com a superfície da raiz e a condição mais adequada para a inserção das células fibroblásticas e crescimento na periodontite crônica . MATERIAL E MÉTODO: Superfícies proximais de 20 dentes com periodontite selecionados foram preparados e divididos em quatro grupos (dez espécimes em cada grupo). I: dentes não tratados (controle): II: curetagem e alisamento radicular; III. aplicação de SRP seguido de rhPDGF (40ng/ml); aplicação de IV: SRP seguido de rh PDGF-BB. Os fibroblastos foram semeados em espécimes radiculares, seguindo-se incubação dos espécimes. Os resultados da contagem celular e forma foram observados pela SEM e avaliados repetidamente dentre de área padrão representativa. RESULTADOS: O Grupo II demonstrou um efeito negativo comparativamente, uma vez que não ocorreram diferenças significativas. O Grupo III mostrou um efeito positivo significativo, maior do que ambos grupos I e II, porém menor do que o Grupo IV. O Grupo IV mostrou o melhor resultado para a quantidade e qualidade celular, onde apresentou diferenças favoráveis quando comparados com todos os outros. CONCLUSÃO: rhPDGF-BB com 25 ng/ml de concentração demonstrou efeito mais positivo na contagem de fibroblastos e as células apresentaram forma mais sadia do que no rhPDGFBB com 50ng/ml. Sugere-se que o rhPDGF-BB apresenta boas possibilidades como um bom agente modulador para inserção de fibroblastos na periodontite crônica.