硫酸软骨素
干细胞
类风湿性关节炎
化学
关节炎
免疫学
细胞生物学
医学
糖胺聚糖
生物
生物化学
作者
Van Dat Bui,Jueun Jeon,Van Hieu Duong,Sol Shin,Jungmi Lee,Farrokhroo Ghahari,Chan Ho Kim,Yu Jin Jo,Won‐Kyo Jung,Wooram Um,Jae Hyung Park
标识
DOI:10.1016/j.jconrel.2024.08.050
摘要
For the non-invasive treatment of rheumatoid arthritis (RA), a chondroitin sulfate C (CSC)-based dissolving microneedles (cMN) was prepared to deliver human adipose stem cell-derived extracellular vesicles (hASC-EV) into inflamed joints. Owing to their anti-inflammatory function, the hASC-EV-bearing cMN (EV@cMN) significantly suppressed activated fibroblast-like synoviocytes (aFLS) and M1 macrophages (M1), which are responsible for the progression of RA. In addition, EV@cMN facilitated the chondrogenic differentiation of bone marrow-derived stem cells. In mice with collagen-induced arthritis, EV@cMN efficiently delivered both hASC-EV and CSC to inflamed joints. Interestingly, pro-inflammatory cytokines in the inflamed joints were remarkably downregulated by the synergistic effect of CSC and hASC-EV. Consequently, as judged from the overall clinical score and joint swelling, EV@cMN showed an outstanding therapeutic effect, even comparable to the wild-type mice, without significant adverse effects. Overall, EV@cMN might have therapeutic potential for RA by efficiently delivering CSC and hASC-EV into the inflamed joints in a non-invasive manner.
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