软骨发生
软骨
化学
骨关节炎
细胞生物学
再生(生物学)
软骨细胞
生物物理学
生物化学
细胞
解剖
医学
病理
生物
替代医学
作者
Xianming Wang,Yu Cai,Cuixi Wu,Jiamin Liang,Kea-Tiong Tang,Zefeng Lin,Lingling Chen,Yao Lu,Qing Wang
标识
DOI:10.1186/s12951-023-02036-5
摘要
Abstract The development of osteoarthritis (OA) correlates with the expansion of senescent cells in cartilage, which contributes to an inflammatory microenvironment that accelerates matrix degradation and hampers cartilage generation. To address OA, we synthesized small copper sulfide nanoparticles functionalized with anti-beta-2-microglobulin antibodies (B2M-CuS NPs) that catalyze the formation of toxic •OH from H 2 O 2 via peroxidase-like activity. These B2M-CuS NPs are specifically targeted to induce apoptosis in senescent chondrocytes while showing no toxicity toward normal chondrocytes. Furthermore, B2M-CuS NPs enhance the chondrogenesis of normal chondrocytes. Thus, B2M-CuS NPs can effectively treat OA by clearing senescent chondrocytes and promoting cartilage regeneration after intra-articular injection into the knee joints of surgery-induced OA mice. This study uses smart nanomaterials to treat OA with a synergistic strategy that both remodels senescent cartilage and creates a pro-chondrogenic microenvironment.
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