Center of Orthopedics, Traumatology, and Spinal Cord Injury, Heidelberg University Hospital, Heidelberg, Germany.
Institute of Biomaterials, University of Erlangen-Nuremberg, Erlangen, Germany.
J Biomed Mater Res A. 2020 Sep;108(9):1806-1815. doi: 10.1002/jbm.a.36945. Epub 2020 Apr 21.
Mesoporous bioactive glass nanoparticles (MBGNs) based on the SiO -P O -CaO system have demonstrated promising properties for the local delivery of therapeutically active ions with the aim to improve their osteogenic properties. Manganese (Mn) has been identified as a candidate ion for local application in bone tissue engineering applications. It remains unknown how SiO -P O -CaO-based MBGNs influence human bone marrow-derived mesenchymal stromal cells (BMSCs) in terms of viability, proliferation, and differentiation and how these features can be modified by the addition of Mn to the MBGNs' composition. Therefore, in this study, MBGNs (composition in mol%: 50 SiO , 40 CaO, 10 P O ) and its Mn-doped derivate 5Mn-MBGNs (composition in mol%: 50 SiO , 35 CaO, 10 P O , 5 MnO) were applied to a culture of BMSCs in two different concentrations. With increasing concentration, 5Mn-MBGNs supported osteogenic differentiation and enhanced the upregulation of genes encoding for extracellular matrix proteins but also negatively influenced cell viability and proliferation. When applied in lower concentrations, MBGNs showed not only viability- and growth-enhancing effects but also significant pro-osteogenic features-however, these positive properties deteriorated with increasing concentration. Two major conclusions can be drawn from this study: (a) supplementation with Mn enhances the osteogenic properties of MBGNs in a dose-dependent manner and (b) MBGNs constitute an attractive vector for therapeutically active ions since it exhibits an intrinsic pro-osteogenic potential that can be improved and/or modified by incorporation of therapeutically active ions. Future studies should focus on the evaluation of further candidate ions that are known to influence osteogenic differentiation positively.
基于 SiO2-P2O5-CaO 系统的介孔生物活性玻璃纳米颗粒(MBGNs)已被证明具有局部递送治疗活性离子的有前途的特性,目的是提高其成骨特性。锰(Mn)已被确定为局部应用于骨组织工程应用的候选离子。目前尚不清楚基于 SiO2-P2O5-CaO 的 MBGNs 如何影响人骨髓间充质基质细胞(BMSCs)的活力、增殖和分化,以及如何通过向 MBGNs 组成中添加 Mn 来改变这些特性。因此,在这项研究中,MBGNs(摩尔%组成:50SiO2、40CaO、10P2O5)及其 Mn 掺杂衍生物 5Mn-MBGNs(摩尔%组成:50SiO2、35CaO、10P2O5、5MnO)被应用于 BMSCs 的培养物中,浓度分为两种。随着浓度的增加,5Mn-MBGNs 支持成骨分化,并增强了细胞外基质蛋白编码基因的上调,但也对细胞活力和增殖产生负面影响。当以较低浓度应用时,MBGNs 不仅具有增强活力和生长的作用,而且还具有显著的促成骨特性-然而,这些积极特性随浓度的增加而恶化。从这项研究中可以得出两个主要结论:(a)Mn 的补充以剂量依赖的方式增强 MBGNs 的成骨特性,(b)MBGNs 构成治疗活性离子的有吸引力的载体,因为它具有内在的促成骨潜力,可以通过掺入治疗活性离子来改善和/或修饰。未来的研究应集中在评估已知对成骨分化有积极影响的进一步候选离子。