软骨发生
再生(生物学)
材料科学
壳聚糖
关节软骨
微球
软骨
生物医学工程
微泡
自愈水凝胶
细胞生物学
骨关节炎
化学工程
高分子化学
医学
解剖
化学
生物
病理
小RNA
工程类
生物化学
替代医学
基因
作者
Rachel Liang,Zhaoxu Li,Xu Qu,Shengtao Wang,Dongxu Chen,Peng Gui,Mingzhou Chen,Wei Peng,Jian Su
标识
DOI:10.1016/j.matdes.2025.113876
摘要
A diverse range of biological materials has been widely used for the management of injuries to joint cartilage. However, suboptimal outcomes in cartilage repair are often due to inappropriate host immune responses and inadequate microenvironments for chondrogenesis. Therefore, there is a need to develop innovative hydrogel systems with immunomodulatory capabilities that promote a favorable environment for cartilage regeneration. In this study, we fabricated a Chitosan Methacryloyl (CSMA) hydrogel and incorporated exosomes derived from lipopolysaccharide (LPS)-activated NR8383 macrophages stimulated with Epigallocatechin gallate (EGCG) (EGCG-exo). Additionally, Kartogenin (KGN)-incorporated poly (lactic-co-glycolic acid) (PLGA) microspheres (KGN μS) were added to the hydrogel to stimulate chondrogenic differentiation of recruited BMSCs upon KGN release. The immunomodulatory and pro-chondrogenic properties of the CSMA-EGCG-exo@KGN μS microsphere-gel system were evaluated both in vitro and in vivo. The CSMA-EGCG-exo@KGN μS system not only demonstrated macrophage reprogramming properties but also enhanced BMSC recruitment and promoted chondrogenesis, leading to improved cartilage regeneration in a rabbit model of cartilage lesions. Looking forward, the CSMA-EGCG-exo@KGN μS microsphere-gel system holds significant potential for clinical translation as a pro-regenerative implant material for the treatment of cartilage injuries.
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