当向SaOS-2细胞中间歇性添加17β-雌二醇时,可刺激矿化骨结节形成

L. Rao, L.J.-F. Liu,, T. Murray, E. McDermott
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引用次数: 5

摘要

现在已经确定雌激素抑制骨吸收。然而,它对骨形成的影响仍然存在争议。我们研究了17 β -雌二醇(E2)对SaOS-2骨肉瘤细胞长期培养中矿化骨结节形成的影响。我们发现SaOS-2细胞形成矿化结节,在电镜下显示出具有活性成骨细胞、被包裹的骨细胞、细胞外胶原原纤维和羟基磷灰石沉积的骨结构,使该系统成为体外研究骨形成的有效模型。从第3天开始,在48小时的培养基变化周期中间歇添加E2 6小时,导致矿化骨结节数量和面积以及碱性磷酸酶活性的剂量依赖性刺激。总之,我们首次报道了E2对培养的人成骨细胞矿化骨结节形成的刺激作用。
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17β-Estradiol Stimulates Mineralized Bone Nodule Formation when Added Intermittently to SaOS-2 Cells
It is now well established that estrogen inhibits bone resorption. However, its effect on bone formation remains controversial. We studied the effect of 17beta-estradiol (E2) on mineralized bone nodule formation in long-term cultures of osteosarcoma SaOS-2 cells. We showed that SaOS-2 cells formed mineralized nodules which under electron microscopy revealed a bone structure with active osteoblasts, entrapped osteocytes, extracellular collagen fibrils and hydroxyapatite deposits, making this system a valid model to study bone formation in vitro. Intermittent addition of E2 for 6 hours during a 48-hour cycle of changes of medium, starting from day 3, resulted in a dose-dependent stimulation of mineralized bone nodule number and area, as well as alkaline phosphatase activity. In conclusion, we report for the first time a stimulatory effect of E2 on mineralized bone nodule formation in human osteoblasts in culture.
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