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基于硫酸软骨素的微针用于经皮递送干细胞衍生的细胞外囊泡以治疗类风湿性关节炎。

Chondroitin sulfate-based microneedles for transdermal delivery of stem cell-derived extracellular vesicles to treat rheumatoid arthritis.

机构信息

School of Chemical Engineering, College of Engineering, Sungkyunkwan University (SKKU), Suwon 16419, Republic of Korea.

Marine Integrated Biomedical Technology Center, The National Key Research Institutes in Universities, Pukyong National University, Busan 48513, Republic of Korea; Major of Biomedical Engineering, Division of Smart Healthcare, College of Information Technology and Convergence and New-senior Healthcare Innovation Center (BK21 Plus), Pukyong National University, Busan 48513, Republic of Korea.

出版信息

J Control Release. 2024 Nov;375:105-115. doi: 10.1016/j.jconrel.2024.08.050. Epub 2024 Sep 6.

Abstract

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.

摘要

为了非侵入性治疗类风湿关节炎(RA),我们制备了一种基于硫酸软骨素 C(CSC)的溶解微针(cMN),将人脂肪干细胞衍生的细胞外囊泡(hASC-EV)递送到发炎的关节中。由于其抗炎功能,负载 hASC-EV 的 cMN(EV@cMN)显著抑制了负责 RA 进展的活化成纤维样滑膜细胞(aFLS)和 M1 巨噬细胞(M1)。此外,EV@cMN 促进了骨髓来源干细胞的软骨分化。在胶原诱导性关节炎的小鼠中,EV@cMN 能够有效地将 hASC-EV 和 CSC 递送到发炎的关节中。有趣的是,CSC 和 hASC-EV 的协同作用显著下调了发炎关节中的促炎细胞因子。因此,从整体临床评分和关节肿胀来看,EV@cMN 表现出出色的治疗效果,甚至可以与野生型小鼠相媲美,没有明显的不良反应。总体而言,EV@cMN 可能通过非侵入性方式将 CSC 和 hASC-EV 有效递送到发炎的关节中,从而为 RA 提供治疗潜力。

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