Department of Orthopaedic Surgery, Stanford University Medical Center, Stanford, California, USA.
J Biomed Mater Res A. 2010 Jul;94(1):234-40. doi: 10.1002/jbm.a.32686.
Periprosthetic osteolysis of joint replacements caused by wear debris is a significant complication of joint replacements. Polymethylmethacrylate (PMMA) particles have been shown to inhibit osteogenic differentiation, but the molecular mechanism has not been previously determined. In this study, we exposed differentiating MC3T3-E1 preostoblast cells to PMMA particles and determined the changes that occurred with respect to p38 mitogen-activated protein kinase (MAPK) activity and the transforming growth factor (TGF)-beta1 and bone morphogenetic protein (BMP) signaling pathways. In the absence of particles, MC3T3-E1 cells demonstrate activation of p38 MAPK on day 8 of differentiation; however, when treated with PMMA particles, differentiating MC3T3-E1 cells demonstrate the suppression of p38 activity on day 8 and show activation of p38 on days 1 and 4. On day 4 of particle exposure, the differentiating MC3T3-E1 cells show significant downregulation of TGF-beta1 expression, which is involved in osteoblast differentiation, and a significant upregulation of the expression of BMP3 and Sclerostin (SOST), which are negative regulators of osteoblast differentiation. By day 8 of particle exposure, the changes in TGF-beta1, BMP3, and SOST expression are opposite of those seen on day 4. This study has demonstrated the distinct changes in the molecular profile of MC3T3-E1 cells during particle-induced inhibition of osteoblast differentiation. (c) 2010 Wiley Periodicals, Inc. J Biomed Mater Res, 2010.
关节置换术后假体周围骨溶解是关节置换术的一种严重并发症。已证实聚甲基丙烯酸甲酯(PMMA)颗粒能抑制成骨细胞分化,但分子机制尚未确定。在这项研究中,我们将分化中的 MC3T3-E1 前成骨细胞暴露于 PMMA 颗粒下,并确定相对于 p38 有丝分裂原激活蛋白激酶(MAPK)活性和转化生长因子(TGF)-β1 及骨形态发生蛋白(BMP)信号通路发生的变化。在无颗粒存在的情况下,MC3T3-E1 细胞在分化的第 8 天显示出 p38 MAPK 的激活;然而,当用 PMMA 颗粒处理时,分化中的 MC3T3-E1 细胞在第 8 天显示出 p38 活性的抑制,并在第 1 天和第 4 天显示出 p38 的激活。在颗粒暴露的第 4 天,分化中的 MC3T3-E1 细胞显示出与成骨细胞分化有关的 TGF-β1 表达的显著下调,以及 BMP3 和 Sclerostin(SOST)表达的显著上调,SOST 是成骨细胞分化的负调控因子。在颗粒暴露的第 8 天,TGF-β1、BMP3 和 SOST 表达的变化与第 4 天相反。本研究证明了在颗粒诱导的成骨细胞分化抑制过程中 MC3T3-E1 细胞的分子谱发生了明显变化。(c)2010 年 Wiley 期刊公司。J 生物医学材料研究,2010。