Hao Junxiang, Bai Baoshuai, Ci Zheng, Tang Jincheng, Hu Guanhuai, Dai Chengxiang, Yu Mengyuan, Li Meng, Zhang Wei, Zhang Yixin, Ren Wenjie, Hua Yujie, Zhou Guangdong
Research Institute of Plastic Surgery, Weifang Medical University, Weifang, Shandong, China.
National Tissue Engineering Center of China, Shanghai, China.
Bioact Mater. 2021 Dec 18;14:97-109. doi: 10.1016/j.bioactmat.2021.12.013. eCollection 2022 Aug.
Physiological repair of large-sized bone defects is great challenging in clinic due to a lack of ideal grafts suitable for bone regeneration. Decalcified bone matrix () is considered as an ideal bone regeneration scaffold, but low cell seeding efficiency and a poor osteoinductive microenvironment greatly restrict its application in large-sized bone regeneration. To address these problems, we proposed a novel strategy of bone regeneration units () based on microgels produced by photo-crosslinkable and microfluidic techniques, containing both the osteogenic ingredient and vascular endothelial growth factor () for accurate biomimic of an osteoinductive microenvironment. The physicochemical properties of microgels could be precisely controlled and the microgels effectively promoted adhesion, proliferation, and osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) . were successfully constructed by seeding BMSCs onto microgels, which achieved reliable bone regeneration . Finally, by integrating the advantages of in bone regeneration and the advantages of scaffolds in 3D morphology and mechanical strength, a -loaded framework successfully regenerated bone tissue with the desired 3D morphology and effectively repaired a large-sized bone defect of rabbit tibia. The current study developed an ideal bone biomimetic microcarrier and provided a novel strategy for bone regeneration and large-sized bone defect repair.
由于缺乏适用于骨再生的理想移植物,临床上大尺寸骨缺损的生理性修复极具挑战性。脱钙骨基质(DBM)被认为是一种理想的骨再生支架,但低细胞接种效率和不良的骨诱导微环境极大地限制了其在大尺寸骨再生中的应用。为了解决这些问题,我们基于光交联和微流控技术制备的微凝胶提出了一种新型骨再生单元(BRUs)策略,该微凝胶同时包含成骨成分骨形态发生蛋白-2(BMP-2)和血管内皮生长因子(VEGF),用于精确模拟骨诱导微环境。微凝胶的物理化学性质能够被精确控制,并且微凝胶有效地促进了骨髓间充质干细胞(BMSCs)的黏附、增殖和成骨分化。通过将BMSCs接种到微凝胶上成功构建了BRUs,实现了可靠的骨再生。最后,通过整合BRUs在骨再生方面的优势以及3D打印支架在三维形态和机械强度方面的优势,一种负载BRUs的3D打印框架成功地再生出具有所需三维形态的骨组织,并有效地修复了兔胫骨的大尺寸骨缺损。当前的研究开发了一种理想的骨仿生微载体,并为骨再生和大尺寸骨缺损修复提供了一种新策略。