Department of Orthopedics and Trauma Surgery, Medical University Graz, Graz, Austria.
Department of Polymer Engineering and Science, Montanuniversitaet Leoben, Leoben, Austria.
J Mater Sci Mater Med. 2017 Sep 5;28(10):155. doi: 10.1007/s10856-017-5969-5.
The biodegradable magnesium-based implants have been widely utilized in medical orthopedic applications in recent years. We have recently shown that direct culture on Pure Mg and Mg2Ag alloys lead to a progressive differentiation impairment of MC3T3-E1 pre-osteoblasts. In this study, we aimed to analyze the apoptotic reaction of MC3T3-E1 cells in response to the direct culture on Pure Mg, Mg2Ag and Extreme High Pure Mg (XHP Mg) alloy samples. Our results demonstrated that long-term culturing of MC3T3-E1 cells on Pure Mg and Mg2Ag alloys induce time-dependent expression of active caspase-3 (active casp-3) and cleaved PARP-1 (cl. PARP-1), the hallmark of apoptosis reactions concomitant with a significant increase in the number of dead cells. However, direct culture on XHP Mg material results in a lower number of dead cells in comparison to Pure Mg and Mg2Ag alloys. Furthermore, XHP Mg materials influence expression of apoptotic markers in a process resembles that of observed in osteogenic condition apparently indicative of MC3T3-E1 osteodifferentiation. This study indicates that Mg alloy samples mediated differential apoptotic reactions of MC3T3-E1 cells can be ascribed to factors such as distinct topography and hydrophobicity features of Mg material surfaces, contrasting nature/composition of corrosion products as well as different impurities of these materials. Therefore, initial Mg alloys surface preparation, controlling the growth and composition of corrosion products and Mg alloys purity enhancement are necessary steps towards optimizing the Mg alloys usage in medical orthopedic applications.
近年来,可生物降解的镁基植入物在医学骨科应用中得到了广泛的应用。我们最近表明,直接在纯镁和 Mg2Ag 合金上培养会导致 MC3T3-E1 前成骨细胞的分化逐渐受损。在这项研究中,我们旨在分析 MC3T3-E1 细胞对纯镁、Mg2Ag 和超高纯镁(XHP Mg)合金样品直接培养的凋亡反应。我们的研究结果表明,MC3T3-E1 细胞在纯镁和 Mg2Ag 合金上长期培养会导致活性 caspase-3(活性 casp-3)和裂解多聚(ADP-核糖)聚合酶-1(cl. PARP-1)的表达随时间推移而增加,这是凋亡反应的特征,同时死亡细胞的数量显著增加。然而,与纯镁和 Mg2Ag 合金相比,直接在 XHP Mg 材料上培养会导致死亡细胞数量减少。此外,XHP Mg 材料对凋亡标志物的表达的影响类似于在成骨条件下观察到的情况,这显然表明 MC3T3-E1 成骨分化。这项研究表明,镁合金样品介导的 MC3T3-E1 细胞的不同凋亡反应可归因于镁材料表面的形貌和疏水性特征、腐蚀产物的性质/组成以及这些材料的不同杂质等因素。因此,初始镁合金表面处理、控制腐蚀产物的生长和组成以及提高镁合金纯度是优化镁合金在医学骨科应用中的必要步骤。