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首页> 外文期刊>Angle Orthodontist >The role of heme oxygenase-1 in mechanical stress- and lipopolysaccharide-induced osteogenic differentiation in human periodontal ligament cells.
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The role of heme oxygenase-1 in mechanical stress- and lipopolysaccharide-induced osteogenic differentiation in human periodontal ligament cells.

机译:血红素加氧酶-1在机械应力和脂多糖诱导的人牙周膜细胞成骨分化中的作用。

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摘要

OBJECTIVE: To investigate the mechanisms through which mechanical stress and lipopolysaccharide treatment modulate osteoblastic differentiation in periodontal ligament cells. MATERIALS AND METHODS: Cells were treated with lipopolysaccharide and/or mechanical strain applied with a Flexercell Strain Unit. Protein expression and mRNA were analyzed by Western blotting and reverse transcription-polymerase chain reaction, respectively. RESULTS: When lipopolysaccharide was co-applied with mechanical strain, the increase in the expression of bone morphogenetic protein-2, bone morphogenetic protein-7, and Runx2 mRNA seen with mechanical strain alone was restricted, but heme oxygenase-1 expression was further enhanced. Furthermore, pretreatment with an inhibitor of heme oxygenase-1 or inhibitors of p38, mitogen-activated protein kinase, JNK, phosphoinositide 3-kinases, protein kinase G, and nuclear factor kappaB restricted osteogenic differentiation induced by the application of lipopolysaccharide and mechanical strain. CONCLUSIONS: These results suggest that orthodontic force-induced osteogenesis in alveolar bone is inhibited by the accompanying periodontal inflammation via the upregulation of heme oxygenase-1 expression. Thus, the heme oxygenase-1 pathway could provide a possible therapeutic strategy to improve bone formation in orthodontic treatment.
机译:目的:探讨机械应力和脂多糖治疗调节牙周膜细胞成骨细胞分化的机制。材料与方法:用脂多糖和/或施加Flexercell应变装置的机械应变处理细胞。分别通过蛋白质印迹和逆转录-聚合酶链反应分析蛋白质表达和mRNA。结果:当脂多糖与机械应变共同应用时,仅机械应变时骨形态发生蛋白2,骨形态发生蛋白7和Runx2 mRNA的表达受到限制,但血红素加氧酶-1的表达进一步增强。此外,用血红素加氧酶-1抑制剂或p38抑制剂,有丝分裂原激活的蛋白激酶,JNK,磷酸肌醇3激酶,蛋白激酶G和核因子kappaB进行的预处理限制了脂多糖和机械应变的应用诱导的成骨分化。结论:这些结果表明,正畸力诱导的牙槽骨成骨被伴随的牙周炎症通过血红素加氧酶-1表达的上调所抑制。因此,血红素加氧酶-1途径可以提供一种可能的治疗策略,以改善正畸治疗中的骨形成。

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