Inflammation-Targeted Celastrol Nanodrug Attenuates Collagen- Induced Arthritis through NF-κB and Notch1 Pathways

被引:155
作者
An, Lemei [1 ]
Li, Zhanrong [1 ]
Shi, Liuqi [1 ]
Wang, Liujun [1 ]
Wang, Yong [2 ]
Jin, Lin [1 ]
Shuai, Xintao [2 ]
Li, Jingguo [1 ]
机构
[1] Zhengzhou Univ, Henan Prov Peoples Hosp, Peoples Hosp, Zhengzhou 450003, Peoples R China
[2] Sun Yat Sen Univ, Sch Mat Sci & Engn, PCFM Lab, Minist Educ, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
rheumatoid arthritis; celastrol; ROS sensitive; NF-kappa B; Notch1; macrophage; NANOPARTICLES; SIRNA; ANGIOGENESIS; MACROPHAGES; ACTIVATION; EXPRESSION; APOPTOSIS; CELLS;
D O I
10.1021/acs.nanolett.0c03279
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rheumatoid arthritis (RA) is a systemic inflammatory disorder which can cause bone and cartilage damage leading to disability, yet the treatment remains unsatisfactory nowadays. Celastrol (Cel) has shown antirheumatic activity against RA. However, the frequent parenteral delivery and poor water solubility of Cel restrict its further therapeutic applications. Here, aiming at effectively overcoming the poor water solubility and short half-life of Cel to boost its beneficial effects for treating RA, we developed a polymeric micelle for Cel delivery based on a reactive oxygen species (ROS) sensitive polymer. Our results demonstrated that Cel may inhibit the repolarization of macrophages toward the proinflammatory M1 pheno-type via regulating the NF-kappa B and Notch1 pathways, which resulted in significantly decreased secretion of multiple pro-inflammatory cytokines to suppress the RA progression. Consequently, the Cel-loaded micelle effectively alleviated the major RA-associated symptoms including articular scores, ankle thickness, synovial inflammation, bone erosion, and cartilage degradation.
引用
收藏
页码:7728 / 7736
页数:9
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