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首页> 外文期刊>Cell Structure and Function >GLUCOCORTICOIDS INDUCE MINERALIZATION COUPLED WITH BONE PROTEIN EXPRESSION WITHOUT INFLUENCE ON GROWTH OF A HUMAN OSTEOBLASTIC CELL LINE
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GLUCOCORTICOIDS INDUCE MINERALIZATION COUPLED WITH BONE PROTEIN EXPRESSION WITHOUT INFLUENCE ON GROWTH OF A HUMAN OSTEOBLASTIC CELL LINE

机译:糖皮质激素诱导矿物质化与骨蛋白表达耦合,而对人成骨细胞细胞系的生长没有影响

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Mineralization was induced by glucocorticoid treatment in a human osteoblastic cell line derived from normal bone in vitro, designated SV-HFO, immortalized with simian virus 40 (CHIBA, H. ct al. (1993). Jpn. J. Cancer Res., 84: 290-297). Mineralization was revealed by electron microscopy, von Kossa staining and electron spectroscopic analysis, which indicated that the Ca/P ratio was approximately 1.70, corresponding to the value of hydroxyapatite. The effect was dose- (10(-8)-10(-6) M) and time-dependent (days 7-28), was greatest at day 28, and was preceded by expression of alkaline phosphatase (ALP) and osteopontin (OPN). The ALP activity induced was highest at day 7, whereas OPN reached its highest level at day 28. When the induction of ALP activity was inhibited by 10(-4) M levamisole, mineralization of SV-HFO cells by glucocorticoid treatment was markedly reduced, suggesting that elevated ALP activity in the early phase is important in the mineralization of human osteoblastic cells. Glucocorticoid treatment did not alter cell proliferation. These results indicated that glucocorticoids play crucial roles in the formation of mineralized matrix in human osteoblasts by inducing differentiation of SV-HFO cells without modulating their proliferative activity. [References: 51]
机译:在体外衍生自正常骨骼的人类成骨细胞系(称为SV-HFO)中,糖皮质激素处理可诱导矿化,该细胞系被猿猴病毒40永生化(CHIBA,H。ct等人,(1993)。Jpn。J. Cancer Res。,84 :290-297)。通过电子显微镜,冯·科萨(von Kossa)染色和电子光谱分析揭示了矿化作用,表明Ca / P比约为1.70,与羟磷灰石的值相对应。效果是剂量-(10(-8)-10(-6)M)和时间依赖性(7-28天),在第28天最大,并先于碱性磷酸酶(ALP)和骨桥蛋白( OPN)。诱导的ALP活性在第7天最高,而OPN在第28天达到最高水平。当10(-4)M左旋咪唑抑制ALP活性诱导时,糖皮质激素处理可明显减少SV-HFO细胞的矿化,提示在早期阶段升高的ALP活性对于人类成骨细胞的矿化很重要。糖皮质激素治疗不会改变细胞增殖。这些结果表明,糖皮质激素通过诱导SV-HFO细胞分化而不调节其增殖活性,在人成骨细胞中矿化基质的形成中起关键作用。 [参考:51]

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