Wei Shuai, Wang Yu, Sun Yu, Gong Leilei, Dai Xiu, Meng Haoye, Xu Wenjing, Ma Jianxiong, Hu Qian, Ma Xinlong, Peng Jiang, Gu Xiaosong
Tianjin Hospital, Tianjin University, No. 406 Jiefang South Road, Hexi District, Tianjin 300211, China; Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Neural Regeneration Co-Innovation Center of Jiangsu Province, Nantong University, No. 19 Qixiu Road, Chongchuan District, Nantong 226001, China; Senior Department of Orthopedics, Beijing Key Lab of Regenerative Medicine in Orthopedics, The 1th Medical Center of PLA General Hospital, No. 28 Fuxing Road, Haidian District, Beijing 100853, China.
Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Neural Regeneration Co-Innovation Center of Jiangsu Province, Nantong University, No. 19 Qixiu Road, Chongchuan District, Nantong 226001, China; Senior Department of Orthopedics, Beijing Key Lab of Regenerative Medicine in Orthopedics, The 1th Medical Center of PLA General Hospital, No. 28 Fuxing Road, Haidian District, Beijing 100853, China.
Int J Biol Macromol. 2023 Apr 30;235:123861. doi: 10.1016/j.ijbiomac.2023.123861. Epub 2023 Mar 2.
Compared with most nondegradable or slowly degradable bone repair materials, bioactive biodegradable porous scaffolds with certain mechanical strengths can promote the regeneration of both new bone and vasculature while the cavity created by their degradation can be replaced by the infiltration of new bone tissue. Mineralized collagen (MC) is the basic structural unit of bone tissue, and silk fibroin (SF) is a natural polymer with adjustable degradation rates and superior mechanical properties. In this study, a three-dimensional porous biomimetic composite scaffold with a two-component SF-MC system was constructed based on the advantages of both materials. The spherical mineral agglomerates of the MC were uniformly distributed on the surface and inside the SF skeleton, which ensured good mechanical properties while regulating the degradation rate of the scaffold. Second, the SF-MC scaffold had good osteogenic induction of bone marrow mesenchymal stem cells (BMSCs) and preosteoblasts (MC3T3-E1) and also promoted the proliferation of MC3T3-E1 cells. Finally, in vivo 5 mm cranial defect repair experiments confirmed that the SF-MC scaffold stimulated vascular regeneration and promoted new bone regeneration in vivo by means of in situ regeneration. Overall, we believe that this low-cost biomimetic biodegradable SF-MC scaffold with many advantages has some clinical translation prospects.
与大多数不可降解或缓慢降解的骨修复材料相比,具有一定机械强度的生物活性可生物降解多孔支架能够促进新骨和血管的再生,同时其降解产生的空腔可被新骨组织的长入所替代。矿化胶原(MC)是骨组织的基本结构单元,而丝素蛋白(SF)是一种具有可调节降解速率和优异机械性能的天然聚合物。在本研究中,基于两种材料的优势构建了一种具有双组分SF-MC体系的三维多孔仿生复合支架。MC的球形矿物团聚体均匀分布在SF骨架的表面和内部,这在确保良好机械性能的同时调节了支架的降解速率。其次,SF-MC支架对骨髓间充质干细胞(BMSC)和成骨前体细胞(MC3T3-E1)具有良好的成骨诱导作用,还促进了MC3T3-E1细胞的增殖。最后,体内5mm颅骨缺损修复实验证实,SF-MC支架通过原位再生刺激了体内血管再生并促进了新骨再生。总体而言,我们认为这种具有诸多优势的低成本仿生可生物降解SF-MC支架具有一定的临床转化前景。