State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Sciences & Medical Engineering, Southeast University, Nanjing, 210096, PR China; Department of Spine Surgery, Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, Jiangsu Province, 210028, PR China; Department of Orthopedics, Nanjing Lishui Hospital of Traditional Chinese Medicine, Nanjing, 211299, PR China.
State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Sciences & Medical Engineering, Southeast University, Nanjing, 210096, PR China.
Biomaterials. 2022 Nov;290:121862. doi: 10.1016/j.biomaterials.2022.121862. Epub 2022 Oct 18.
Fusion of endothelial monolayer for rapid reendothelialization is the key to vascular transplantation, which is crucial for remodeling long-distance (≥10 mm) vascular injury (LDVJ) and reducing the long-term repair period. Although silk fibroin (SF) has been widely prepared as a scaffold to repair vascular injuries, it is still challenging to remodel LDVJs. The design and manufacture of functional scaffolds with a rapid reendothelialization enhancement effect are helpful to solve this problem. Here, we developed a well-designed functional magnetic scaffold (MDP) with a temperature-controlled switch, intelligently regulating the release of magnetic nanoparticles (MNPs) to induce macrophages migration and M2 polarization. The results show that the radial support force of MDP is appropriately five times higher than that of pure silk fibroin scaffold (SFC), and the degradation of MDP is delayed, which is beneficial to maintaining the integrity of the scaffold. MDP induces the migration of macrophages, upregulates the expression of repair cytokines such as TGF-β, IL-10 and VEGF, and promotes the proliferation of mouse aortic vascular smooth muscle (MOVAS) cells. More importantly, the enhanced migration of macrophages at the phase transition temperature is more conducive to the proliferation and accumulation of vascular repair-related cells, which is conducive to rapid reendothelialization. In addition, MDP also significantly regulates the polarization of macrophages to M2 type, which is conducive to the secretion of repair cytokines to further promote vascular recovery. The evaluation of endothelial cells' adhesion and function also proved that MDP could increase the expression of vascular endothelial cadherin (VE-Cad) and collagen IV (COL IV) and has the potential for rapid reendothelialization. The replacement model in vivo animal experiments further proved that MDP exhibited a better repair effect than SFC, providing a new option for the repair of LDVJ in the future.
内皮单层细胞融合是血管移植快速再内皮化的关键,对于重塑长距离(≥10mm)血管损伤(LDVJ)和缩短长期修复期至关重要。尽管丝素蛋白(SF)已被广泛制备作为修复血管损伤的支架,但重塑 LDVJ 仍然具有挑战性。设计和制造具有快速再内皮化增强效果的功能性支架有助于解决这个问题。在这里,我们开发了一种具有温度控制开关的精心设计的功能磁性支架(MDP),智能调节磁性纳米颗粒(MNPs)的释放,以诱导巨噬细胞迁移和 M2 极化。结果表明,MDP 的径向支撑力适当比纯丝素蛋白支架(SFC)高五倍,并且 MDP 的降解延迟,这有利于维持支架的完整性。MDP 诱导巨噬细胞迁移,上调修复细胞因子如 TGF-β、IL-10 和 VEGF 的表达,并促进小鼠主动脉血管平滑肌(MOVAS)细胞的增殖。更重要的是,相变温度下增强的巨噬细胞迁移更有利于血管修复相关细胞的增殖和积累,有利于快速再内皮化。此外,MDP 还显著调节巨噬细胞向 M2 型的极化,有利于修复细胞因子的分泌,进一步促进血管恢复。对内皮细胞黏附和功能的评估也证明了 MDP 可以增加血管内皮钙黏蛋白(VE-Cad)和胶原 IV(COL IV)的表达,具有快速再内皮化的潜力。体内动物实验的替代模型进一步证明,MDP 比 SFC 表现出更好的修复效果,为未来 LDVJ 的修复提供了新的选择。