类风湿性关节炎
重编程
医学
免疫学
癌症研究
经济衰退
炎症
关节炎
滑膜炎
滑膜
巨噬细胞
免疫系统
发病机制
病理
作者
Jiahao Lin,Li J,Yue Wu,Xinqiang Hu,Hao Wei,Menghuan Li,Xue Hu,Zhong Luo,Kaiyong Cai,Yan Hu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-07-22
标识
DOI:10.1021/acsnano.6c05740
摘要
Rheumatoid arthritis (RA) is a systemic autoimmune disease that causes serious joint damage and functional loss, which is predominantly associated with the aberrant activation of synovial macrophages. Herein, we report an injectable ion-coordinated bionic lubricant to efficiently reprogram synovial macrophages into pro-regenerative phenotypes for RA treatment. For this purpose, rhein (Rh)-modified PEGylated liposomes were integrated with coenzyme Q10 (CoQ10) for macrophage-targeted delivery (LipQ10-Rh), which were subsequently embedded into dynamic hyaluronic acid (HA)-based hydrogel matrices cross-linked by acylhydrazone bonding and Zn 2+ ion-mediated coordination (HALZ). Owing to the intrinsic reversibility of the dynamic bonding network, the HALZ lubricant could be facilely injected into RA-affected joint cavity and provide immediate relief through biolubrication. Meanwhile, the LipQ10-Rh liposomes and Zn ions could be gradually released from the dynamic hydrogels and taken in by synovial macrophages, where the Zn ions could activate the anti-inflammatory metabolism while CoQ10 alleviated mitochondrial ROS stress to restore their reparative functions, which acted in a cooperative manner to reprogram the inflammatory synovial macrophages into pro-regenerative phenotypes. In vivo results evidently suggested that the injectable HALZ biolubricant efficiently abolished RA-associated joint damage on rat models in a durable manner, providing an approach for improving RA recession in the clinic.
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