间充质干细胞
脐带
软骨细胞
骨关节炎
微泡
软骨
干细胞
细胞生物学
帘布衬里
细胞
化学
医学
小RNA
生物
免疫学
体外
成体干细胞
病理
内皮干细胞
生物化学
解剖
替代医学
基因
作者
Hongfu Cao,Wei Ma,Xiaolin Cui,Yuan Liu,Yuhan Liu,Siyan Deng,Tun Yuan,Yujiang Fan,Qiguang Wang,Shouxin Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-07-13
卷期号:17 (14): 13358-13376
被引量:39
标识
DOI:10.1021/acsnano.3c01612
摘要
As chondrocytes from osteoarthritic cartilage usually exhibit aging and senescent characteristics, targeting aging chondrocytes could be a potential therapeutic strategy. In this study, exosomes derived from umbilical cord-derived mesenchymal stem cells (UCMSC-EXOs) combined with the chondrocyte-targeting capacity and controlled-release system were proposed for osteoarthritis (OA) treatment via rejuvenating aging chondrocytes. The essential functional miRNAs within UCMSC-EXOs were investigated, with the p53 signaling pathway identified as the key factor. To improve the therapeutic efficiency and retention time of UCMSC-EXOs in vivo, the exosomes (EXOs) were engineered on membranes with a designed chondrocyte-targeting polymers, and encapsulated within thiolated hyaluronic acid microgels to form a "two-phase" releasing system, which synergistically facilitated the repair of OA cartilage in a rat model. Together, this study highlighted the rejuvenating effects of UCMSC-EXOs on OA chondrocytes and the potential to combine with chondrocyte-targeting and sustained-release strategies toward a future cell-free OA treatment.
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