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姜黄素预处理的 ADMSCs 衍生的小细胞外囊泡通过抑制氧化应激和软骨细胞凋亡对骨关节炎发挥增强的保护作用。

Curcumin primed ADMSCs derived small extracellular vesicle exert enhanced protective effects on osteoarthritis by inhibiting oxidative stress and chondrocyte apoptosis.

机构信息

Shanghai Key Laboratory of Orthopedic Implants, Department of Orthopedics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200011, China.

Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200011, China.

出版信息

J Nanobiotechnology. 2022 Mar 9;20(1):123. doi: 10.1186/s12951-022-01339-3.

Abstract

Osteoarthritis (OA) is a common joint disease caused by progressive articular cartilage degeneration and destruction. Currently, there are no disease-modifying agents officially approved for OA patients. In this study, curcumin was loaded into adipose tissue-derived mesenchymal stem cells (ADMSCs)-derived small extracellular vesicle (ADMSCs-sEV) to synergistically exert chondro-protective effects in vitro and in vivo. We found curcumin primed ADMSCs derived sEV (sEV-CUR) exhibited an enhanced protective effect compared with free curcumin and ADMSCs-sEV in TBHP-induced chondrocytes. Moreover, our study demonstrated sEV-CUR more effectively down-regulated TBHP-induced oxidative stress and chondrocyte apoptosis in vitro. In OA mice model, our results indicated that sEV-CUR showed an improved cartilage protection, as biweekly intra-articular injection of sEV-CUR more efficaciously alleviated oxidative stress and chondrocyte apoptosis in OA cartilage. Overall, our findings showed sEV-CUR exhibited enhanced chondro-protective effects and holds great potential on the recovery of articular cartilage loss and destruction in OA patients.

摘要

骨关节炎(OA)是一种常见的关节疾病,由进行性关节软骨退变和破坏引起。目前,尚无针对 OA 患者的疾病修饰药物获得正式批准。在这项研究中,姜黄素被载入脂肪组织来源的间充质干细胞(ADMSCs)衍生的小细胞外囊泡(ADMSCs-sEV)中,以协同发挥体外和体内的软骨保护作用。我们发现姜黄素预处理的 ADMSCs 衍生的 sEV(sEV-CUR)与游离姜黄素和 ADMSCs-sEV 相比,在 TBHP 诱导的软骨细胞中表现出增强的保护作用。此外,我们的研究表明 sEV-CUR 更有效地下调了 TBHP 诱导的体外氧化应激和软骨细胞凋亡。在 OA 小鼠模型中,我们的结果表明 sEV-CUR 显示出改善的软骨保护作用,因为每隔一周向关节内注射 sEV-CUR 更有效地减轻了 OA 软骨中的氧化应激和软骨细胞凋亡。总的来说,我们的研究结果表明 sEV-CUR 表现出增强的软骨保护作用,对于恢复 OA 患者的关节软骨缺失和破坏具有很大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de72/8905866/54ab44d379da/12951_2022_1339_Fig1_HTML.jpg

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