Li Jiaying, Ma Jinjin, Feng Qian, Xie En, Meng Qingchen, Shu Wenmiao, Wu Junxi, Bian Liming, Han Fengxuan, Li Bin
State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection and Interdisciplinary Sciences (RAD-X), Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, The First Affiliated Hospital, Suzhou Medical College, Soochow University, Suzhou, Jiangsu 215006, China.
Orthopedic Institute, Department of Orthopaedic Surgery, The First Affiliated Hospital, Suzhou Medical College, Soochow University, Suzhou, Jiangsu, China.
Research (Wash D C). 2023;6:0021. doi: 10.34133/research.0021. Epub 2023 Jan 10.
The critical factor determining the in vivo effect of bone repair materials is the microenvironment, which greatly depends on their abilities to promote vascularization and bone formation. However, implant materials are far from ideal candidates for guiding bone regeneration due to their deficient angiogenic and osteogenic microenvironments. Herein, a double-network composite hydrogel combining vascular endothelial growth factor (VEGF)-mimetic peptide with hydroxyapatite (HA) precursor was developed to build an osteogenic microenvironment for bone repair. The hydrogel was prepared by mixing acrylated β-cyclodextrins and octacalcium phosphate (OCP), an HA precursor, with gelatin solution, followed by ultraviolet photo-crosslinking. To improve the angiogenic potential of the hydrogel, QK, a VEGF-mimicking peptide, was loaded in acrylated β-cyclodextrins. The QK-loaded hydrogel promoted tube formation of human umbilical vein endothelial cells and upregulated the expression of angiogenesis-related genes, such as , , and , in bone marrow mesenchymal stem cells. Moreover, QK could recruit bone marrow mesenchymal stem cells. Furthermore, OCP in the composite hydrogel could be transformed into HA and release calcium ions facilitating bone regeneration. The double-network composite hydrogel integrated QK and OCP showed obvious osteoinductive activity. The results of animal experiments showed that the composite hydrogel enhanced bone regeneration in skull defects of rats, due to perfect synergistic effects of QK and OCP on vascularized bone regeneration. In summary, improving the angiogenic and osteogenic microenvironments by our double-network composite hydrogel shows promising prospects for bone repair.
决定骨修复材料体内效果的关键因素是微环境,这在很大程度上取决于它们促进血管生成和骨形成的能力。然而,植入材料因其血管生成和成骨微环境不足,远非引导骨再生的理想候选材料。在此,开发了一种将血管内皮生长因子(VEGF)模拟肽与羟基磷灰石(HA)前体相结合的双网络复合水凝胶,以构建用于骨修复的成骨微环境。该水凝胶是通过将丙烯酸化的β-环糊精和HA前体八钙磷酸酯(OCP)与明胶溶液混合,然后进行紫外光交联制备而成。为了提高水凝胶的血管生成潜力,将VEGF模拟肽QK负载到丙烯酸化的β-环糊精中。负载QK的水凝胶促进人脐静脉内皮细胞的管腔形成,并上调骨髓间充质干细胞中血管生成相关基因(如 、 和 )的表达。此外,QK可以招募骨髓间充质干细胞。此外,复合水凝胶中的OCP可以转化为HA并释放钙离子,促进骨再生。整合了QK和OCP的双网络复合水凝胶表现出明显的骨诱导活性。动物实验结果表明,由于QK和OCP对血管化骨再生具有完美的协同作用,复合水凝胶增强了大鼠颅骨缺损处的骨再生。总之,通过我们的双网络复合水凝胶改善血管生成和成骨微环境,在骨修复方面显示出广阔的前景。