润滑
微泡
材料科学
骨关节炎
软骨
纳米技术
软骨细胞
遗传增强
医学
病理
生物
复合材料
基因
生物化学
解剖
小RNA
替代医学
作者
Manyu Chen,Yan Lu,Yuhan Liu,Quanying Liu,Siyan Deng,Yuan Liu,Xiaolin Cui,Jie Liang,Xingdong Zhang,Yujiang Fan,Qiguang Wang
标识
DOI:10.1002/adma.202312559
摘要
Abstract Abnormal silencing of fibroblast growth factor (FGF) signaling significantly contributes to joint dysplasia and osteoarthritis (OA); However, the clinical translation of FGF18‐based protein drugs is hindered by their short half‐life, low delivery efficiency and the need for repeated articular injections. This study proposes a CRISPR/Cas9‐based approach to effectively activate the FGF18 gene of OA chondrocytes at the genome level in vivo, using chondrocyte‐affinity peptide (CAP) incorporated hybrid exosomes (CAP/FGF18‐hyEXO) loaded with an FGF18‐targeted gene‐editing tool. Furthermore, CAP/FGF18‐hyEXO are encapsulated in methacrylic anhydride‐modified hyaluronic (HAMA) hydrogel microspheres via microfluidics and photopolymerization to create an injectable microgel system (CAP/FGF18‐hyEXO@HMs) with self‐renewable hydration layers to provide persistent lubrication in response to frictional wear. Together, the injectable CAP/FGF18‐hyEXO@HMs, combined with in vivo FGF18 gene editing and continuous lubrication, have demonstrated their capacity to synergistically promote cartilage regeneration, decrease inflammation, and prevent ECM degradation both in vitro and in vivo, holding great potential for clinical translation.
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