EPAS1, a Dexamethasone-Inducible Gene in Osteoblasts, Inhibits Osteoblastic Differentiation

N. Ijichi, K. Ikeda, M. Fujita, T. Usui, T. Urano, Kotaro Azuma, Y. Ouchi, Kuniko Horie-Inoue, S. Inoue
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引用次数: 3

Abstract

Glucocorticoid-induced osteoporosis is a clinical problem in patients under chronic steroid therapy. To delineate the action of glucocorticoids on osteoblasts, we performed microarray analysis using rat primary osteoblasts and identified several glucocorticoid target genes. We validated the dexamethasone-induced upregulation of CCAAT/ enhancer-binding protein delta (C/EBP ), endothelial PAS-domain protein 1 (EPAS1), matrix Gla protein (MGP), and nerve growth factor inducible-B (NGFI-B) expression by quantitative real time-polymerase chain reaction (qPCR). EPAS1 overexpression inhibited, whereas dominant-negative EPAS1 overexpression enhanced the upregulation of osteoblastic marker genes and the mineralization in ST2 mesenchymal cells under the simulated osteoblastogenesis conditions. These results suggest that glucocorticoids could inhibit osteoblastic differentiation by regulating its target genes, as exemplified by EPAS1.
成骨细胞中地塞米松诱导基因EPAS1抑制成骨细胞分化
糖皮质激素所致骨质疏松症是慢性类固醇治疗患者的临床问题。为了描述糖皮质激素对成骨细胞的作用,我们对大鼠原代成骨细胞进行了微阵列分析,并鉴定了几个糖皮质激素靶基因。我们通过定量实时聚合酶链反应(qPCR)验证了地塞米松诱导的CCAAT/增强子结合蛋白δ (C/EBP)、内皮pas -结构域蛋白1 (EPAS1)、基质Gla蛋白(MGP)和神经生长因子诱导-b (NGFI-B)表达上调。EPAS1过表达抑制了模拟成骨条件下ST2间充质细胞成骨标记基因的上调和矿化,而EPAS1过表达的显性阴性则增强了成骨标记基因的上调和矿化。这些结果表明糖皮质激素可能通过调控其靶基因来抑制成骨细胞分化,如EPAS1。
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