雷奈酸锶改善成骨细胞与钛基质的相互作用:增加细胞增殖、分化和基质矿化。

William Querido, Marcos Farina, Karine Anselme
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引用次数: 14

摘要

我们描述了雷奈酸锶对成骨细胞与不同钛基质相互作用的直接影响。我们的目标是更好地了解这种药物在提高骨植入物疗效方面的潜力。在细胞培养中分别用0.12和0.5 mM Sr(2+)的雷奈酸锶处理。我们分析了细胞对药物在钛基板上的反应,这些钛基板的表面形貌是通过酸蚀刻、电侵蚀、喷砂和机械加工获得的。处理保留了细胞与基质的初始粘附、细胞形状参数(面积、长宽比、圆度和固体度)以及细胞在凹槽表面上的方向。然而,两种浓度的药物都增加了所有底物中的细胞增殖。此外,碱性磷酸酶活性和矿化基质的产生呈剂量依赖性增加,具有骨组织的典型特征。在不同基质中观察到的效果是相似的。综上所述,雷奈酸锶改善了成骨细胞与钛基质的相互作用,促进了成骨细胞的增殖和向成熟成骨细胞的分化,并促进了所有基质的骨样矿化基质的产生。这项研究强调了雷奈酸锶在提高骨植入物临床成功率方面的重要作用,特别是在骨质疏松症患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Strontium ranelate improves the interaction of osteoblastic cells with titanium substrates: Increase in cell proliferation, differentiation and matrix mineralization.

Strontium ranelate improves the interaction of osteoblastic cells with titanium substrates: Increase in cell proliferation, differentiation and matrix mineralization.

Strontium ranelate improves the interaction of osteoblastic cells with titanium substrates: Increase in cell proliferation, differentiation and matrix mineralization.

Strontium ranelate improves the interaction of osteoblastic cells with titanium substrates: Increase in cell proliferation, differentiation and matrix mineralization.

We describe direct effects of strontium ranelate on the interaction of osteoblastic cells with different titanium substrates. Our goal was to better understand the potential of this drug for improving the efficacy of bone implants. Treatment was done with 0.12 and 0.5 mM Sr(2+) of strontium ranelate in cell culture. We analyzed cell response to the drug on titanium substrates with surface topographies obtained using acid etching, electro-erosion processing, sandblasting, and machine-tooling. Treatment preserved the initial cell adhesion to the substrates, cell shape parameters (area, aspect ratio, circularity, and solidity), and the orientation of cells on grooved surfaces. However, both concentrations of the drug increased cell proliferation in all substrates. Moreover, a dose-dependent increase in alkaline phosphatase activity and in the production of mineralized matrix with typical features of bone tissue was shown. The observed effects were similar in the different substrates. In conclusion, strontium ranelate improved the interaction of osteoblastic cells with titanium substrates, increasing cell proliferation and differentiation into mature osteoblasts and the production of bone-like mineralized matrix for all substrates. This study highlights a promising role of strontium ranelate on enhancing the clinical success of bone implants, particularly in patients with osteoporosis.

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