A MnO2 nanosheets doping double crosslinked hydrogel for cartilage defect repair through alleviating inflammation and guiding chondrogenic differentiation

IF 12.8 1区 医学 Q1 ENGINEERING, BIOMEDICAL Biomaterials Pub Date : 2024-10-18 DOI:10.1016/j.biomaterials.2024.122875
Feilong Zhao , Zhibo Jia , Liyang Zhang , Guodong Liu , Junfei Li , Jianming Zhao , Yajie Xie , Lu Chen , Hongyu Jiang , Wei He , Aiyuan Wang , Jiang Peng , Yudong Zheng
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Abstract

The inflammatory microenvironment and inferior chondrogenesis are major symptoms after cartilage defect. Although various modifications strategies associated with hydrogels exhibit remarkable capacity of pro-cartilage regeneration, the adverse effect by prolonging inflammation is still formidable to hamper potential biomedical applications of different hydrogel implants. Herein, inspired by the repair microenvironment of articular cartilage defects, an injectable, immunomodulatory, and chondrogenic L-MNS-CMDA hydrogel is prepared through grafting vinyl and catechol groups to chitosan macromolecules using amide reaction, then further loading MnO2 nanosheets (MNS). The double crosslinking of photopolymerization and catechol oxidative polymerization endows L-MNS-CMDA hydrogel with preferable mechanical property, affording a suitable mechanical support for cartilage defect repair. Additionally, the robust tissue adhesion capability stemming from catechol groups guarantees the long-term retention of the hydrogel in the defect site. Meanwhile, L-MNS-CMDA hydrogel decomposes exogenous and intracellular H2O2 into O2 and H2O, to effectively alleviate cellular oxidative stress caused by long-term hypoxia. Under the synergies of catechol groups and MNS, L-MNS-CMDA hydrogel not only inhibits macrophages polarizing into M1 phenotype, but encourages them turn into M2 phenotype, thereby, reconstructing an immunization friendly microenvironment to ultimately enhance cartilage regeneration. Predictably, the hydrogel markedly induces rat bone marrow mesenchymal stem cells differentiating into chondrocytes by expressing abundant glycosaminoglycan and type II collagen. A cartilage defect model of rat knee joint indicates that L-MNS-CMDA hydrogel visually regulate the early inflammatory response of post-implantation, and facilitate cartilage regeneration and recovery of joint function after 12 weeks of post-implantation. All in all, this multifunctional L-MNS-CMDA hydrogel exhibits superior immunomodulatory and chondrogenic properties, holding immense clinical potential in the treatment of cartilage defects.
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一种掺杂二氧化锰纳米片的双交联水凝胶,可通过缓解炎症和引导软骨分化修复软骨缺损。
炎症性微环境和软骨生成低下是软骨缺损后的主要症状。尽管与水凝胶相关的各种改良策略都显示出了促进软骨再生的显著能力,但延长炎症时间的不良影响仍然十分严重,阻碍了不同水凝胶植入物在生物医学领域的潜在应用。本文受关节软骨缺损修复微环境的启发,利用酰胺反应将乙烯基和邻苯二酚基团接枝到壳聚糖大分子上,然后进一步载入 MnO2 纳米片(MNS),制备了一种可注射、具有免疫调节和软骨再生能力的 L-MNS-CMDA 水凝胶。光聚合和邻苯二酚氧化聚合的双重交联赋予 L-MNS-CMDA 水凝胶优越的机械性能,为软骨缺损修复提供了合适的机械支持。此外,儿茶酚基团产生的强大组织粘附能力保证了水凝胶在缺损部位的长期保留。同时,L-MNS-CMDA 水凝胶能将外源性和细胞内的 H2O2 分解为 O2 和 H2O,有效缓解长期缺氧造成的细胞氧化应激。在儿茶酚基团和 MNS 的协同作用下,L-MNS-CMDA 水凝胶不仅能抑制巨噬细胞向 M1 表型极化,还能促进其向 M2 表型转化,从而重建免疫友好型微环境,最终促进软骨再生。可以预见的是,水凝胶能明显诱导大鼠骨髓间充质干细胞分化为软骨细胞,并表达大量糖胺聚糖和 II 型胶原蛋白。大鼠膝关节软骨缺损模型表明,L-MNS-CMDA 水凝胶可视化调节植入后的早期炎症反应,促进软骨再生,并在植入后 12 周恢复关节功能。总之,这种多功能 L-MNS-CMDA 水凝胶具有卓越的免疫调节和软骨生成特性,在治疗软骨缺损方面具有巨大的临床潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomaterials
Biomaterials 工程技术-材料科学:生物材料
CiteScore
26.00
自引率
2.90%
发文量
565
审稿时长
46 days
期刊介绍: Biomaterials is an international journal covering the science and clinical application of biomaterials. A biomaterial is now defined as a substance that has been engineered to take a form which, alone or as part of a complex system, is used to direct, by control of interactions with components of living systems, the course of any therapeutic or diagnostic procedure. It is the aim of the journal to provide a peer-reviewed forum for the publication of original papers and authoritative review and opinion papers dealing with the most important issues facing the use of biomaterials in clinical practice. The scope of the journal covers the wide range of physical, biological and chemical sciences that underpin the design of biomaterials and the clinical disciplines in which they are used. These sciences include polymer synthesis and characterization, drug and gene vector design, the biology of the host response, immunology and toxicology and self assembly at the nanoscale. Clinical applications include the therapies of medical technology and regenerative medicine in all clinical disciplines, and diagnostic systems that reply on innovative contrast and sensing agents. The journal is relevant to areas such as cancer diagnosis and therapy, implantable devices, drug delivery systems, gene vectors, bionanotechnology and tissue engineering.
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