首页> 外文期刊>Journal of Periodontology >Estrogen regulates expression of osteoprotegerin and RANKL in human periodontal ligament cells through estrogen receptor beta.
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Estrogen regulates expression of osteoprotegerin and RANKL in human periodontal ligament cells through estrogen receptor beta.

机译:雌激素通过雌激素受体β调节人牙周膜细胞中骨保护素和RANKL的表达。

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摘要

BACKGROUND: The function of periodontal ligament (PDL) cells may be affected by estrogen. PDL cells synthesize the receptor activator of nuclear factor-kappa B ligand (RANKL) and its decoy receptor, namely, osteoprotegerin (OPG), which directly controls osteoclastogenesis. The primary aim of this study was to investigate how estrogen affects the expression of OPG and RANKL in human PDL (hPDL) cells. METHODS: We used a short interfering RNA technique to inhibit estrogen receptor beta (ERbeta) expression in hPDL cells; the cells were cultured with a saturating concentration of 17beta-estradiol (10(7) M) for 48 hours. Changes in the expression of OPG and RANKL were determined by reverse transcription-polymerase chain reaction and supported by Western blot analysis. RESULTS: Estradiol caused an increase in OPG expression and decreased RANKL expression in hPDL cells. However, it had no effect on the expression of OPG and RANKL in hPDL-siERbeta (the short interfering RNA to block ER beta) cells. CONCLUSION: Estrogen may play an important role in exerting antiresorptive effects on alveolar bone, at least in part, by increasing the expression level of OPG versus that of RANKL via ERbeta in hPDL cells.
机译:背景:牙周膜(PDL)细胞的功能可能受到雌激素的影响。 PDL细胞合成核因子-κB配体(RANKL)的受体激活剂及其诱饵受体,即直接控制破骨细胞形成的骨保护素(OPG)。这项研究的主要目的是研究雌激素如何影响人PDL(hPDL)细胞中OPG和RANKL的表达。方法:我们使用了一种短干扰RNA技术来抑制hPDL细胞中雌激素受体β(ERbeta)的表达。将细胞与饱和浓度的17β-雌二醇(10(7)M)培养48小时。通过逆转录-聚合酶链反应确定OPG和RANKL表达的变化,并通过蛋白质印迹分析进行支持。结果:雌二醇引起hPDL细胞OPG表达增加,RANKL表达降低。但是,它对hPDL-siERbeta(阻断ER beta的短干扰RNA)细胞中OPG和RANKL的表达没有影响。结论:雌激素可能在通过hPDL细胞中通过ERbeta增加OPG的表达水平相对于RANKL的表达水平至少部分地发挥了对牙槽骨的抗吸收作用的重要作用。

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