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The essential role of glucocorticoids for proper human osteoblast differentiation and matrix mineralization.

机译:糖皮质激素在适当的人类成骨细胞分化和基质矿化中的重要作用。

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摘要

Glucocorticoids (GCs) exert profound effects on bone and are essential for human osteoblast differentiation. However, GCs are still interpreted as negative regulators of bone formation, mainly caused by the detrimental effects on bone after clinical use of GCs. In this paper we emphasize the importance of GCs for proper human osteoblast differentiation and matrix mineralization. We show that human osteoblast differentiation needs to be triggered by GCs in a specific time-window during the early stages of development. Exposure to GCs in the beginning of osteoblast development induces a dose dependent increase in alkaline phosphatase activity and matrix mineralization. GC-induced differentiation stimulated expression of genes involved in bone formation and suppressed genes that negatively regulate bone formation and mineralization. Furthermore we highlight the importance of local cortisol activation in osteoblasts by expression of 11beta-hydroxysteroid dehydrogenase 1 (11beta-HSD1).
机译:糖皮质激素(GCs)对骨骼产生深远的影响,对人类成骨细胞的分化至关重要。但是,GC仍被解释为骨骼形成的负调节剂,主要是由临床使用GC后对骨骼的有害影响引起的。在本文中,我们强调了气相色谱对人类成骨细胞正确分化和基质矿化的重要性。我们表明,人类成骨细胞的分化需要在早期阶段的特定时间窗口中由GC触发。成骨细胞发育开始时接触GC会引起碱性磷酸酶活性和基质矿化的剂量依赖性增加。 GC诱导的分化刺激了参与骨骼形成的基因的表达,并抑制了负面调节骨骼形成和矿化的基因。此外,我们强调了11β-羟基类固醇脱氢酶1(11beta-HSD1)的表达在成骨细胞中局部皮质醇活化的重要性。

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