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用于增强肌腱修复的MnO修饰脱细胞肌腱膜的制备

Fabrication of MnO-Modified Decellularized Tendon Membrane for Enhancing Tendon Repair.

作者信息

Lun Wanqing, Wang Huajun, Li Mengyuan, Ma Jiuzhi, Ding Yilin, Zheng Xiaofei, Cao Xiaodong, Li Qingtao

机构信息

School of Medicine, South China University of Technology, Guangzhou, 510006, P. R. China.

National Engineering Research Centre for Tissue Restoration and Reconstruction, Guangzhou, 510006, P. R. China.

出版信息

Adv Healthc Mater. 2025 Jan;14(1):e2402584. doi: 10.1002/adhm.202402584. Epub 2024 Nov 3.

Abstract

Repairing tendon/ligament injuries is a major challenge in sports medicine. It has been reported that tendon injury healing is hindered by massive production of reactive oxygen species (ROS). Manganese oxides nanoparticles are generally non-toxic, can scavenge ROS, promote tissue regeneration, and hold promise for sustainable nanotechnologies. However, the effective and safe integration of MnO nanoparticles on decellularized scaffold mediating tissue repair is still a great challenge. To address these issues, an in situ MnO-modified decellularized scaffold is developed to enhance tendon regeneration through improving microenvironment. The decellularized fibrous membrane is designed and prepared using the central tendon of the porcine diaphragm. Then MnO nanozymes are in situ grown on the collagen fibers using tannic acid (TA) as cross-linking agent and reducing agent. The results showed that MnO-modified scaffold eliminates excessive accumulation of ROS in cells, protects mitochondrial, and maintains the phenotype of tendon cells in an oxidative stress environment. Notably, it is found that the MnO-modified scaffold exhibits good biocompatibility and is able to promote the tendon healing in the rat patellar tendon defect model. Altogether, this study confirmed that this nanozyme-functionalized decellularized extracellular matrix effectively enhanced tendon repair by scavenging ROS, which provides new strategies for enhancing tendon regeneration.

摘要

修复肌腱/韧带损伤是运动医学中的一项重大挑战。据报道,活性氧(ROS)的大量产生会阻碍肌腱损伤的愈合。氧化锰纳米颗粒通常无毒,能够清除ROS,促进组织再生,有望应用于可持续纳米技术。然而,将MnO纳米颗粒有效且安全地整合到脱细胞支架上以介导组织修复仍然是一个巨大的挑战。为了解决这些问题,开发了一种原位MnO修饰的脱细胞支架,通过改善微环境来增强肌腱再生。利用猪膈肌的中央肌腱设计并制备了脱细胞纤维膜。然后以单宁酸(TA)作为交联剂和还原剂,在胶原纤维上原位生长MnO纳米酶。结果表明,MnO修饰的支架消除了细胞内ROS的过度积累,保护了线粒体,并在氧化应激环境中维持了肌腱细胞的表型。值得注意的是,发现MnO修饰的支架具有良好的生物相容性,并且能够促进大鼠髌腱缺损模型中的肌腱愈合。总之,本研究证实这种纳米酶功能化的脱细胞细胞外基质通过清除ROS有效地增强了肌腱修复,为增强肌腱再生提供了新的策略。

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