Ma Jun, Yu Han, Zhang Xinyu, Xu Zhuoming, Hu Hanyin, Liu Jintao, Ren Peng, Kong Xiangjia, Chen Jiayi, Yang Kun, Wang Xinyu, He Xiaojun, Luo Huanhuan, Chen Gang
Jiaxing University Master Degree Cultivation Base, Zhejiang Chinese Medical University, 899 Guangqiong Road, Jiaxing 314001, P. R. China.
Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, Department of Orthopaedics, The Second Affiliated Hospital of Jiaxing University, 1518 North Huancheng Road, Jiaxing 314000, P. R. China.
ACS Appl Mater Interfaces. 2024 Feb 7;16(5):5582-5597. doi: 10.1021/acsami.3c16544. Epub 2024 Jan 23.
The tendon-bone interface has a complex gradient structure vital for stress transmission and pressure buffering during movement. However, injury to the gradient tissue, especially the tendon and cartilage components, often hinders the complete restoration of the original structure. Here, a metal ion network hydrogel scaffold, with the capability of targeting multitissue, was constructed through the photopolymerization of the LHERHLNNN peptide-modified zeolitic imidazolate framework-8 (LZIF-8) and the WYRGRL peptide-modified magnesium metal-organic framework (WMg-MOF) within the hydrogel scaffold, which could facilitate the directional migration of metal ions to form a dynamic gradient, thereby achieving integrated regeneration of gradient tissues. LZIF-8 selectively migrated to the tendon, releasing zinc ions to enhance collagen secretion and promoting tendon repair. Simultaneously, WMg-MOF migrated to cartilage, releasing magnesium ions to induce cell differentiation and facilitating cartilage regeneration. Infrared spectroscopy confirmed successful peptide modification of nano ZIF-8 and Mg-MOF. Fluorescence imaging validated that LZIF-8/WMg-MOF had a longer retention, indirectly confirming their successful targeting of the tendon-bone interface. In summary, this dual-targeted metal ion network hydrogel scaffold has the potential to facilitate synchronized multitissue regeneration at the compromised tendon-bone interface, offering favorable prospects for its application in the integrated reconstruction characterized by the gradient structure.
肌腱-骨界面具有复杂的梯度结构,对运动过程中的应力传递和压力缓冲至关重要。然而,梯度组织的损伤,尤其是肌腱和软骨成分的损伤,常常阻碍原始结构的完全恢复。在此,通过在水凝胶支架内对LHERHLNNN肽修饰的沸石咪唑酯骨架-8(LZIF-8)和WYRGRL肽修饰的镁基金属有机骨架(WMg-MOF)进行光聚合,构建了一种具有多组织靶向能力的金属离子网络水凝胶支架,其可促进金属离子的定向迁移以形成动态梯度,从而实现梯度组织的整合再生。LZIF-8选择性迁移至肌腱,释放锌离子以增强胶原蛋白分泌并促进肌腱修复。同时,WMg-MOF迁移至软骨,释放镁离子以诱导细胞分化并促进软骨再生。红外光谱证实了纳米ZIF-8和Mg-MOF的肽修饰成功。荧光成像验证了LZIF-8/WMg-MOF具有更长的滞留时间,间接证实了它们对肌腱-骨界面的成功靶向。总之,这种双靶向金属离子网络水凝胶支架具有促进受损肌腱-骨界面多组织同步再生的潜力,为其在具有梯度结构的整合重建中的应用提供了良好前景。