Center of Orthopedics, Traumatology and Spinal Cord Injury, Heidelberg University Hospital, Schlierbacher Landstraße 200a, 69118 Heidelberg, Germany.
ATORG-Aschaffenburg Trauma and Orthopedic Research Group, Center for Trauma Surgery, Orthopedics and Sports Medicine, Klinikum Aschaffenburg-Alzenau, Am Hasenkopf 1, 63739 Aschaffenburg, Germany.
Int J Mol Sci. 2019 Aug 30;20(17):4253. doi: 10.3390/ijms20174253.
Compared to other materials such as 45S5 bioactive glass (BG), β-tricalcium phosphate (β-TCP)-based bone substitutes such as Vitoss show limited material-driven stimulation of osteogenesis and/or angiogenesis. The unfavorable degradation kinetics of β-TCP-based bone substitutes may result in an imbalance between resorption and osseous regeneration. Composite materials like Vitoss BA (Vitoss supplemented with 20 wt % 45S5-BG particles) might help to overcome these limitations. However, the influence of BG particles in Vitoss BA compared to unsupplemented Vitoss on osteogenesis, resorption behavior, and angiogenesis is not yet described. In this study, Vitoss and Vitoss BA scaffolds were seeded with human mesenchymal stromal cells before subcutaneous implantation in immunodeficient mice for 10 weeks. Scaffold resorption was monitored by micro-computed tomography, while osteoid formation and vascularization were assessed by histomorphometry and gene expression analysis. Whilst slightly more osteoid and improved angiogenesis were found in Vitoss BA, maturation of the osteoid was more advanced in Vitoss scaffolds. The volume of Vitoss implants decreased significantly, combined with a significantly increased presence of resorbing cells, whilst the volume remained stable in Vitoss BA scaffolds. Future studies should evaluate the interaction of 45S5-BG with resorbing cells and bone precursor cells in greater detail to improve the understanding and application of β-TCP/45S5-BG composite bone substitute materials.
与 45S5 生物活性玻璃 (BG) 等其他材料相比,基于 β-磷酸三钙 (β-TCP) 的骨替代物,如 Vitoss,对成骨和/或血管生成的材料驱动刺激有限。基于 β-TCP 的骨替代物的不利降解动力学可能导致吸收和骨质再生之间的失衡。像 Vitoss BA(补充有 20wt%45S5-BG 颗粒的 Vitoss)这样的复合材料可能有助于克服这些限制。然而,与未补充 BG 颗粒的 Vitoss 相比,BG 颗粒在 Vitoss BA 中的作用对成骨、吸收行为和血管生成的影响尚未描述。在这项研究中,将人间充质基质细胞接种到 Vitoss 和 Vitoss BA 支架上,然后在免疫缺陷小鼠皮下植入 10 周。通过微计算机断层扫描监测支架的吸收,通过组织形态计量学和基因表达分析评估类骨质形成和血管生成。虽然在 Vitoss BA 中发现了更多的类骨质和改善的血管生成,但 Vitoss 支架中的类骨质成熟度更高。Vitoss 植入物的体积显著减少,同时吸收细胞的存在显著增加,而 Vitoss BA 支架中的体积保持稳定。未来的研究应更详细地评估 45S5-BG 与吸收细胞和骨前体细胞的相互作用,以提高对 β-TCP/45S5-BG 复合骨替代材料的理解和应用。