Wonkwang Bone Regeneration Research Institute, Wonkwang University, Iksan, 570-749 Korea ; Bonecell Biotech Inc., Dunsan-dong, Seo-gu, Daejeon, 302-830 Korea.
Department of Herbal Crop Research, NIHHS, RDA, Eumseong, 369-873 Korea.
Biomater Res. 2015 Aug 25;19:18. doi: 10.1186/s40824-015-0040-4. eCollection 2015.
Angiogenin (ANG) is a potent stimulator of angiogenesis. The aim of this study was to fabricate an ANG-loaded scaffold and to evaluate its angiogenic and osteogenic effects. In this study, we fabricated an ANG-loaded scaffold using bovine bone powder and fibrin glue. We then evaluated the structural, morphological, and mechanical properties of the scaffold and the in vitro release profile of ANG. Cell proliferation, viability, and adhesion were evaluated using endothelial cells in vitro, and angiogenesis and new bone formation were evaluated using a rabbit calvarial defect model in vivo.
Micro-computed tomography imaging showed that the bone powder was uniformly distributed in the scaffold, and scanning electron microscopy showed that the bone powder was bridged by polymerized fibrin. The porosity and compressive strength of the scaffolds were ~60 % and ~0.9 MPa, respectively, and were not significantly altered by ANG loading. In vitro, at 7 days, approximately 0.4 μg and 1.3 μg of the ANG were released from the FB/ANG 0.5 and FB/ANG 2.0, respectively and sustained slow release was observed until 25 days. The released ANG stimulated cell proliferation and adherence and was not cytotoxic. Furthermore, in vivo implantation resulted in enhanced angiogenesis, and new bone formation depended on the amount of loaded ANG.
These studies demonstrate that a fibrin and bone powder scaffold loaded with ANG might be useful to promote bone regeneration by enhanced angiogenesis.
血管生成素(ANG)是一种强有力的血管生成刺激剂。本研究旨在制备 ANG 负载的支架,并评估其血管生成和成骨作用。在这项研究中,我们使用牛骨粉和纤维蛋白胶制备了 ANG 负载的支架。然后,我们评估了支架的结构、形态和机械性能以及 ANG 的体外释放情况。通过体外内皮细胞评估细胞增殖、活力和黏附性,通过兔颅骨缺损模型评估体内血管生成和新骨形成。
微计算机断层扫描成像显示骨粉均匀分布在支架中,扫描电子显微镜显示骨粉由聚合纤维蛋白桥接。支架的孔隙率和压缩强度分别约为 60%和 0.9 MPa,ANG 负载并未显著改变其性能。体外 7 天时,从 FB/ANG 0.5 和 FB/ANG 2.0 中分别释放了约 0.4μg 和 1.3μg 的 ANG,并观察到持续缓慢释放,直至 25 天。释放的 ANG 刺激细胞增殖和黏附,且无细胞毒性。此外,体内植入可促进血管生成,新骨形成取决于负载的 ANG 量。
这些研究表明,负载 ANG 的纤维蛋白和骨粉支架可能通过增强血管生成来促进骨再生。