Martinez Sanchez Adela H, Feyerabend Frank, Laipple Daniel, Willumeit-Römer Regine, Weinberg Annelie, Luthringer Bérengère J C
Helmholtz-Zentrum Geesthacht, Institute of Material Research, Department for Structural Research on Macromolecules, Geesthacht, Germany.
Helmholtz-Zentrum Geesthacht, Institute of Material Research, Department for Structural Research on Macromolecules, Geesthacht, Germany.
Mater Sci Eng C Mater Biol Appl. 2017 Mar 1;72:378-388. doi: 10.1016/j.msec.2016.11.062. Epub 2016 Nov 24.
Biodegradable magnesium (Mg)-based materials are a potential alternative to permanent implants for application in children. Nevertheless effects of those materials on growth plate cartilage and chondrogenesis have not been previously evaluated. In vitro differentiation of ATDC5 cells was evaluated under the influence of pure Mg (PMg), Mg with 10wt% of gadolinium (Mg-10Gd) and Mg with 2wt% of silver (Mg-2Ag) degradation products (extracts) and direct cell culture on the materials. Gene expression showed an inhibitory effect on ATDC5 mineralization with the three extracts and a chondrogenic potential of Mg-10Gd. Cells cultured in Mg-10Gd and Mg-2Ag extracts showed the same proliferation and morphology than cells cultured in growth conditions. Mg-10Gd induced an increase in production of ECM and a bigger cell size, similar to the effects found with differentiation conditions. An increased metabolic activity was observed in cells cultured under the influence of Mg-10Gd extracts, indicated by an acidic pH during most of the culture period. After 7days of culture on the materials, ATDC5 growth, distribution and ECM synthesis were higher on Mg-10Gd samples, followed by Mg-2Ag and PMg, which was influenced by the homogeneity and composition of the degradation layer. This study confirmed the tolerance of ATDC5 cells to Mg-based materials and a chondrogenic effect of Mg-10Gd. Further studies in vitro and in vivo are necessary to evaluate cell reactions to those materials, as well as the effects on bone growth and the biocompatibility of the alloying system in the body.
可生物降解的镁基材料是儿童永久性植入物的潜在替代品。然而,此前尚未评估这些材料对生长板软骨和软骨形成的影响。在纯镁(PMg)、含10wt%钆的镁(Mg-10Gd)和含2wt%银的镁(Mg-2Ag)降解产物(提取物)的影响下,以及在材料上直接进行细胞培养的条件下,评估了ATDC5细胞的体外分化情况。基因表达显示,这三种提取物对ATDC5矿化有抑制作用,而Mg-10Gd具有软骨形成潜力。在Mg-10Gd和Mg-2Ag提取物中培养的细胞与在生长条件下培养的细胞具有相同的增殖和形态。Mg-10Gd诱导细胞外基质(ECM)产生增加且细胞尺寸增大,类似于在分化条件下发现的效果。在Mg-10Gd提取物影响下培养的细胞中观察到代谢活性增加,这在大部分培养期间表现为酸性pH值。在材料上培养7天后,Mg-10Gd样品上的ATDC5生长、分布和ECM合成更高,其次是Mg-2Ag和PMg,这受到降解层的均匀性和组成的影响。本研究证实了ATDC5细胞对镁基材料的耐受性以及Mg-10Gd的软骨形成作用。有必要进行进一步的体外和体内研究,以评估细胞对这些材料的反应,以及对骨骼生长的影响和体内合金系统的生物相容性。