Clinical Research Centre, UCD School of Medicine & Medical Science, Mater Misericordiae University Hospital, Dublin, Ireland.
BMC Musculoskelet Disord. 2010 Sep 15;11:210. doi: 10.1186/1471-2474-11-210.
The Wnt/β-catenin pathway is a major signaling cascade in bone biology, playing a key role in bone development and remodeling. The objectives of this study were firstly, to determine the effects of dexamethasone exposure on Wnt/β-catenin signaling at an intracellular and transcriptional level, and secondly, to assess the phenotypic effects of silencing the Wnt antagonist, Dickkopf-1 (Dkk1) in the setting of dexamethasone exposure.
Primary human osteoblasts were exposed in vitro to 10-8 M dexamethasone over a 72 h time course. The phenotypic marker of osteoblast differentiation was analyzed was alkaline phosphatase activity. Intracellular β-catenin trafficking was assessed using immunoflourescence staining and TCF/LEF mediated transcription was analyzed using a Wnt luciferase reporter assay. Dkk1 expression was silenced using small interfering RNA (siRNA).
Primary human osteoblasts exposed to dexamethasone displayed a significant reductions in alkaline phosphatase activity over a 72 h time course. Immunoflourescence analaysis of β-catenin localization demonstrated a significant reduction in intracytosolic and intranuclear β-catenin in response to dexamethasone exposure. These changes were associated with a reduction of TCF/LEF mediated transcription. Silencing Dkk1 expression in primary human osteoblasts exposed to dexamethasone resulted in an increase in alkaline phosphatase activity when compared to scrambled control.
Wnt/β-catenin signaling plays a key role in regulating glucocorticoid-induced osteoporosis in vitro. Silencing Dkk1 expression rescues dexamethasone-induced suppression of primary human osteoblast differentiation. Targeting of the Wnt/β-catenin signaling pathway offers an exciting opportunity to develop novel anabolic bone agents to treat osteoporosis and disorders of bone mass.
Wnt/β-catenin 信号通路是骨生物学中的主要信号级联,在骨发育和重塑中起着关键作用。本研究的目的首先是确定地塞米松暴露对内源性和转录水平的 Wnt/β-catenin 信号的影响,其次是评估在地塞米松暴露的情况下沉默 Wnt 拮抗剂 Dickkopf-1(Dkk1)的表型效应。
体外将原代人成骨细胞暴露于 10-8 M 地塞米松中,时间为 72 小时。成骨细胞分化的表型标志物通过碱性磷酸酶活性进行分析。使用免疫荧光染色评估细胞内β-catenin 转运,使用 Wnt 荧光素酶报告基因测定分析 TCF/LEF 介导的转录。使用小干扰 RNA(siRNA)沉默 Dkk1 的表达。
在 72 小时的时间过程中,地塞米松暴露的原代人成骨细胞显示碱性磷酸酶活性显著降低。β-catenin 定位的免疫荧光分析表明,地塞米松暴露后细胞内和核内β-catenin 显著减少。这些变化与 TCF/LEF 介导的转录减少有关。在暴露于地塞米松的原代人成骨细胞中沉默 Dkk1 的表达导致碱性磷酸酶活性增加,与对照相比。
Wnt/β-catenin 信号通路在体外调节糖皮质激素诱导的骨质疏松症中起着关键作用。沉默 Dkk1 的表达可挽救地塞米松诱导的原代人成骨细胞分化抑制。靶向 Wnt/β-catenin 信号通路为开发新型促骨合成药物治疗骨质疏松症和骨量异常提供了一个令人兴奋的机会。