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Zoledronate inhibits phosphate and bone morphogenetic protein 2-induced extracellular calcification of vascular smooth muscle cells in vitro

机译:唑来膦酸盐抑制磷酸盐和骨形态发生蛋白2诱导的体外血管平滑肌细胞钙化

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摘要

The aim of this study was to explore the effects of the bisphosphonate zoledronate on calcification induced by inorganic phosphate (Pi) and/or bone morphogenetic protein 2 (BMP-2) and the underlying mechanisms. Primary vascular smooth muscle cells (VSMCs) from rats were treated with 3 mM Pi or 3 mM Pi/BMP-2, with and without addition of zoledronate; 1.4 mM Pi served as a control. Calcium deposits, expression of core binding factor α-1 (Cbfa-1), osteopontin (OPN), parathyroid pituitary-specific transcription factor (Pit)-1 and Pit-2, and Pi uptake of VSMCs was determined. The calcification of VSMCs induced by elevated Pi or Pi/BMP-2 was significantly inhibited by zoledronate. The expression of Cbfa-1, OPN and Pit-1 was increased significantly after treatment with an elevated level of Pi or Pi/BMP-2, and this expression was significantly suppressed by addition of zoledronate. Pi uptake of VSMCs increased following treatment with elevated Pi and significantly decreased by addition of zoledronate. These results indicated that zoledronate effectively inhibited calcification induced by Pi/BMP-2, and this may have been achieved by means of the downregulation of expression of calcification-related proteins and uptake of Pi.
机译:这项研究的目的是探讨双膦酸盐唑来膦酸盐对无机磷酸盐(Pi)和/或骨形态发生蛋白2(BMP-2)诱导的钙化的影响及其潜在机制。用3 mM Pi或3 mM Pi / BMP-2处理大鼠原代血管平滑肌细胞(VSMC),添加或不添加唑来膦酸盐;将1.4 mM Pi用作对照。测定钙沉积,核心结合因子α-1(Cbfa-1),骨桥蛋白(OPN),甲状旁腺垂体特异性转录因子(Pit)-1和Pit-2的表达以及VSMC的Pi摄取。唑来膦酸盐显着抑制Pi或Pi / BMP-2升高引起的VSMC钙化。用升高的Pi或Pi / BMP-2水平处理后,Cbfa-1,OPN和Pit-1的表达显着增加,并且通过添加唑来膦酸盐显着抑制了该表达。用升高的Pi处理后,VSMC的Pi摄取增加,并通过添加唑来膦酸盐显着降低。这些结果表明唑来膦酸盐有效抑制了Pi / BMP-2诱导的钙化,这可能是通过下调钙化相关蛋白的表达和摄取Pi来实现的。

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