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聚甲基丙烯酸甲酯颗粒抑制MC3T3-E1成骨祖细胞的成骨分化。

Polymethylmethacrylate particles inhibit osteoblastic differentiation of MC3T3-E1 osteoprogenitor cells.

作者信息

Chiu Richard, Ma Ting, Smith R Lane, Goodman Stuart B

机构信息

Department of Orthopaedic Surgery, Stanford University Medical Center, 300 Pasteur Drive, Edwards Building, R-116, Stanford, California 94305-5341, USA.

出版信息

J Orthop Res. 2008 Jul;26(7):932-6. doi: 10.1002/jor.20618.

Abstract

Orthopedic wear debris has been implicated as a significant inhibitory factor of osteoblast differentiation. Polymethylmethacrylate (PMMA) particles have been previously shown to inhibit the differentiation of osteoprogenitors in heterogeneous murine marrow stromal cell cultures, but the effect of PMMA particles on pure osteoprogenitor populations remains unknown. In this study, we challenged murine MC3T3-E1 osteoprogenitor cells with PMMA particles during their initial differentiation in osteogenic medium. MC3T3-E1 cultures challenged with PMMA particles showed a gradual dose-dependent decrease in mineralization, cell number, and alkaline phosphatase activity at low particle doses (0.038-0.150% v/v) and complete reduction of these outcome parameters at high particle doses (> or =0.300% v/v). MC3T3-E1 cultures challenged with a high particle dose (0.300% v/v) showed no rise in these outcome parameters over time, whereas cultures challenged with a low particle dose (0.075% v/v) showed a normal or reduced rate of increase compared to controls. Osteocalcin production was not significantly affected by particles at all doses tested. MC3T3-E1 cells grown in conditioned medium from particle-treated MC3T3-E1 cultures showed a significant reduction in mineralization only. These results indicate that direct exposure of MC3T3-E1 osteoprogenitors to PMMA particles results in suppression of osteogenic proliferation and differentiation.

摘要

骨科磨损颗粒被认为是成骨细胞分化的一个重要抑制因素。先前已表明,聚甲基丙烯酸甲酯(PMMA)颗粒可抑制异质性小鼠骨髓基质细胞培养物中骨祖细胞的分化,但PMMA颗粒对纯骨祖细胞群体的影响仍不清楚。在本研究中,我们在成骨培养基中使小鼠MC3T3-E1骨祖细胞在其初始分化过程中接触PMMA颗粒。用PMMA颗粒处理的MC3T3-E1培养物在低颗粒剂量(0.038-0.150% v/v)下,矿化、细胞数量和碱性磷酸酶活性呈逐渐的剂量依赖性下降,而在高颗粒剂量(≥0.300% v/v)下,这些结果参数则完全降低。用高颗粒剂量(0.300% v/v)处理的MC3T3-E1培养物随着时间推移这些结果参数没有升高,而用低颗粒剂量(0.075% v/v)处理的培养物与对照相比显示出正常或降低的增加速率。在所有测试剂量下,骨钙素的产生均未受到颗粒的显著影响。在来自用颗粒处理的MC3T3-E1培养物的条件培养基中生长的MC3T3-E1细胞仅矿化显著减少。这些结果表明,MC3T3-E1骨祖细胞直接接触PMMA颗粒会导致成骨增殖和分化受到抑制。

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