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OP-1(骨形态发生蛋白 7)在聚甲基丙烯酸甲酯颗粒存在的情况下刺激成骨前体细胞分化。

OP-1 (BMP-7) stimulates osteoprogenitor cell differentiation in the presence of polymethylmethacrylate particles.

机构信息

Department of Orthopaedic Surgery, Stanford University Medical Center, Stanford, California, USA.

出版信息

J Biomed Mater Res A. 2010 Aug;94(2):485-8. doi: 10.1002/jbm.a.32712.

Abstract

Polymethylmethacrylate (PMMA) particles have been shown to inhibit the differentiation, proliferation, and mineralization of osteoprogenitor cells in vitro. In this study, we investigated the effects of OP-1 (BMP-7) on the osteogenesis of MC3T3-E1 osteoprogenitor cells exposed to PMMA particles in vitro. MC3T3-E1 cells challenged with PMMA particles on the 1st day of differentiation in osteogenic culture showed a significant dose-dependent decrease in mineralization and alkaline phosphatase expression over a 20-day culture period. Exposure of these cells to OP-1 (200 ng/mL) during days 1-4, 1-20, and 4-20 in the presence of PMMA particles resulted in significant increases in mineralization and alkaline phosphatase expression at all particle doses. Addition of OP-1 to MC3T3-E1 cultures challenged with PMMA particles on the 4th day of differentiation in osteogenic media also resulted in significant increases in mineralization and alkaline phosphatase expression. This study has shown that OP-1 stimulates osteogenesis in MC3T3-E1 osteoprogenitor cells that have been inhibited by PMMA particles. Local administration of OP-1 to the site of osteolysis may be a potential adjunctive therapy to reverse the bone destruction due to wear particles.

摘要

聚甲基丙烯酸甲酯(PMMA)颗粒已被证明可抑制体外成骨前体细胞的分化、增殖和矿化。在本研究中,我们研究了 OP-1(BMP-7)对体外暴露于 PMMA 颗粒的 MC3T3-E1 成骨前体细胞成骨的影响。在成骨培养中分化第 1 天用 PMMA 颗粒刺激 MC3T3-E1 细胞,在 20 天的培养期间,矿化和碱性磷酸酶表达呈显著的剂量依赖性下降。在 PMMA 颗粒存在的情况下,将这些细胞在第 1-4、1-20 和 4-20 天暴露于 OP-1(200ng/ml),在所有颗粒剂量下均导致矿化和碱性磷酸酶表达显著增加。在成骨培养基中第 4 天分化时用 PMMA 颗粒刺激 MC3T3-E1 培养物,然后添加 OP-1,也导致矿化和碱性磷酸酶表达显著增加。本研究表明,OP-1 可刺激被 PMMA 颗粒抑制的 MC3T3-E1 成骨前体细胞的成骨。局部给予 OP-1 到骨溶解部位可能是逆转由于磨损颗粒导致的骨破坏的潜在辅助治疗方法。

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