正畸力作用下人牙周韧带中OPG和RANKL mRNA和蛋白的表达与存在

L. Otero, D. García, L. Wilches-Buitrago
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引用次数: 17

摘要

目的研究不同正畸力对人牙周韧带(hPDL)中NFkB配体受体激活因子(RANKL)和骨保护素(OPG)的表达和浓度的影响。方法对32例患者右前臼齿施加4oz或7oz的正畸力,持续7天。左第一前磨牙没有装牙。7天后,拔除前磨牙,按提示进行治疗。采用定量逆转录聚合酶链反应(qRT-PCR)检测OPG和RANKL mRNA表达,ELISA检测PDL受压侧和张力侧OPG和RANKL蛋白浓度。数据进行方差分析和Tukey检验。结果对照牙与实验牙张压侧的RANKL浓度比较,差异有统计学意义(P < 0.0001)。rrankl mRNA的表达在拉伸侧和压缩侧增加(P < 0.0001)。OPG在任何组间均无统计学意义。实验组与对照组RANKL/OPG蛋白比值变化差异有统计学意义(P < 0.0001)。结论:在加载正畸力的hPDL中,RANKL蛋白水平升高,表明RANKL蛋白在初始正畸力放置时有助于骨建模。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression and Presence of OPG and RANKL mRNA and Protein in Human Periodontal Ligament with Orthodontic Force
OBJECTIVE The objective of this study is to investigate the expression and concentration of ligand receptor activator of NFkB (RANKL) and osteoprotegerin (OPG) in human periodontal ligament (hPDL) with orthodontic forces of different magnitudes. METHODS Right premolars in 32 patients were loaded with 4oz or 7oz of orthodontic force for 7 days. Left first premolars were not loaded. After 7 days, premolars were extracted for treatment as indicated. OPG and RANKL mRNA expressions were measured by quantitative reverse transcription polymerase chain reaction (qRT-PCR), and ELISA was used to assess OPG and RANKL protein concentration in compression and tension sides of PDL. Data were subjected to analysis of variance and Tukey tests. RESULTS There was statistically significant difference in RANKL concentration on comparing control teeth with tension and compression sides of the experimental teeth (P < 0.0001). The expression of mRNA RANKL was increased in the tension and compression sides with 4oz (P < 0.0001). OPG did not show statistically significant association with any group. Changes in RANKL/OPG protein ratio in experimental and control groups showed statistically significant difference (P < 0.0001). CONCLUSIONS RANKL protein levels are elevated in hPDL loaded with orthodontic forces, suggesting that RANKL protein contributes to bone modeling in response to the initial placement of orthodontic force.
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