Roland Laura, Grau Michael, Matena Julia, Teske Michael, Gieseke Matthias, Kampmann Andreas, Beyerbach Martin, Murua Escobar Hugo, Haferkamp Heinz, Gellrich Nils-Claudius, Nolte Ingo
Small Animal Clinic, University of Veterinary Medicine Hannover, Foundation, Hannover D-30559, Germany.
Division of Medicine Clinic III, Hematology, Oncology and Palliative Medicine, University of Rostock, Rostock D-18057, Germany.
Int J Mol Sci. 2015 Dec 22;17(1):1. doi: 10.3390/ijms17010001.
For healing of critically sized bone defects, biocompatible and angiogenesis supporting implants are favorable. Murine osteoblasts showed equal proliferation behavior on the polymers poly-ε-caprolactone (PCL) and poly-(3-hydroxybutyrate)/poly-(4-hydroxybutyrate) (P(3HB)/P(4HB)). As vitality was significantly better for PCL, it was chosen as a suitable coating material for further experiments. Titanium implants with 600 µm pore size were evaluated and found to be a good implant material for bone, as primary osteoblasts showed a vitality and proliferation onto the implants comparable to well bottom (WB). Pure porous titanium implants and PCL coated porous titanium implants were compared using Live Cell Imaging (LCI) with Green fluorescent protein (GFP)-osteoblasts. Cell count and cell covered area did not differ between the implants after seven days. To improve ingrowth of blood vessels into porous implants, proangiogenic factors like Vascular Endothelial Growth Factor (VEGF) and High Mobility Group Box 1 (HMGB1) were incorporated into PCL coated, porous titanium and magnesium implants. An angiogenesis assay was performed to establish an in vitro method for evaluating the impact of metallic implants on angiogenesis to reduce and refine animal experiments in future. Incorporated concentrations of proangiogenic factors were probably too low, as they did not lead to any effect. Magnesium implants did not yield evaluable results, as they led to pH increase and subsequent cell death.
对于临界尺寸骨缺损的愈合,生物相容性好且能支持血管生成的植入物是有利的。小鼠成骨细胞在聚ε-己内酯(PCL)和聚(3-羟基丁酸酯)/聚(4-羟基丁酸酯)(P(3HB)/P(4HB))聚合物上表现出相同的增殖行为。由于PCL的细胞活力明显更好,因此被选为进一步实验的合适涂层材料。对孔径为600 µm的钛植入物进行了评估,发现它是一种良好的骨植入材料,因为原代成骨细胞在该植入物上的活力和增殖情况与孔底相当。使用绿色荧光蛋白(GFP)-成骨细胞的活细胞成像(LCI)技术对纯多孔钛植入物和PCL涂层多孔钛植入物进行了比较。七天后,两种植入物之间的细胞计数和细胞覆盖面积没有差异。为了促进血管长入多孔植入物,将血管内皮生长因子(VEGF)和高迁移率族蛋白B1(HMGB1)等促血管生成因子掺入PCL涂层的多孔钛和镁植入物中。进行了一项血管生成试验,以建立一种体外方法来评估金属植入物对血管生成的影响,以便在未来减少和优化动物实验。促血管生成因子的掺入浓度可能过低,因为它们没有产生任何效果。镁植入物没有得出可评估的结果,因为它们导致pH值升高并随后导致细胞死亡。