Department of Oral and Maxillofacial Surgery, School of Stomatology, China Medical University, Liaoning Institute of Dental Research, Shenyang, Liaoning 110002, P.R. China.
Department of Plastic Surgery, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning 110002, P.R. China.
Mol Med Rep. 2018 Apr;17(4):5830-5836. doi: 10.3892/mmr.2018.8579. Epub 2018 Feb 8.
Scaffold fabrication and biocompatibility are crucial for successful bone tissue engineering. Nanometer hydroxyapatite (nHAP) combined with collagen (COL) is frequently utilized as a suitable osseous scaffold material. Furthermore, growth factors, including bone morphogenetic protein‑2 (BMP‑2), are used to enhance the scaffold properties. The present study used blending and freeze‑drying methods to develop a BMP‑2‑nHAP‑COL scaffold. An ELISA was performed to determine the BMP‑2 release rate from the scaffold. Flow cytometry was used to identify rat bone marrow‑derived mesenchymal stem cells (BMSCs) prior to their combination with the scaffold. Scanning electron microscopy was used to observe the scaffold structure and BMSC morphology following seeding onto the scaffold. BMSCs were also used to assess the biological compatibility of the scaffold in vitro. BMP‑2‑nHAP‑COL and nHAP‑COL scaffolds were assessed alongside the appropriate control groups. Cells were counted to determine early cell adhesion. Cell Counting kit‑8 and alkaline phosphatase assays were used to detect cell proliferation and differentiation, respectively. Gross morphology confirmed that the BMP‑2‑nHAP‑COL scaffold microstructure conformed to the optimal characteristics of a bone tissue engineering scaffold. Furthermore, the BMP‑2‑nHAP‑COL scaffold exhibited no biological toxicity and was demonstrated to promote BMSC adhesion, proliferation and differentiation. The BMP‑2‑nHAP‑COL scaffold had good biocompatibility in vitro, and may therefore be modified further to construct an optimized scaffold for future bone tissue engineering.
支架的制造和生物相容性对于成功的骨组织工程至关重要。纳米羟基磷灰石(nHAP)与胶原蛋白(COL)结合常用于作为合适的骨支架材料。此外,还使用生长因子,包括骨形态发生蛋白 2(BMP-2)来增强支架性能。本研究采用共混和冷冻干燥方法制备 BMP-2-nHAP-COL 支架。通过 ELISA 测定支架中 BMP-2 的释放率。采用流式细胞术鉴定大鼠骨髓间充质干细胞(BMSCs),然后将其与支架结合。扫描电子显微镜观察支架结构和接种支架后的 BMSC 形态。还使用 BMSCs 在体外评估支架的生物相容性。BMP-2-nHAP-COL 和 nHAP-COL 支架与相应的对照组一起进行评估。通过计数细胞来确定早期细胞黏附。细胞计数试剂盒-8 和碱性磷酸酶测定分别用于检测细胞增殖和分化。大体形态学证实 BMP-2-nHAP-COL 支架的微观结构符合骨组织工程支架的最佳特性。此外,BMP-2-nHAP-COL 支架没有生物毒性,并且被证明可以促进 BMSC 的黏附、增殖和分化。BMP-2-nHAP-COL 支架在体外具有良好的生物相容性,因此可以进一步修饰以构建用于未来骨组织工程的优化支架。