活性氧
一氧化氮
类风湿性关节炎
炎症
滑膜炎
纳米医学
医学
DNA损伤
免疫学
药理学
癌症研究
化学
材料科学
DNA
生物化学
内科学
纳米技术
纳米颗粒
作者
Yuxuan Ma,Zhangwei Lu,Bin Jia,Ye Shi,Jun Dong,Shuoxing Jiang,Zhe Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-08-02
卷期号:16 (8): 12520-12531
被引量:51
标识
DOI:10.1021/acsnano.2c03991
摘要
Rheumatoid arthritis (RA) severely threatens human health by causing inflammation, swelling, and pain in the joints and resulting in persistent synovitis and irreversible joint disability. In the development of RA, pro-inflammatory M1 macrophages, which express high levels of reactive oxygen species (ROS) and nitric oxide (NO), induce synovial inflammation and bone erosion. Eliminating ROS and NO in the inflamed joints is a potential RA therapeutic approach, which can drive the transition of pro-inflammatory M1 macrophages to the anti-inflammatory M2 phenotype. Taking advantage of the intrinsic ROS- and NO-scavenging capability of DNA molecules, herein, we report the development of folic acid-modified triangular DNA origami nanostructures (FA-tDONs) for targeted RA treatment. FA-tDONs could efficiently scavenge ROS and NO and actively target M1 macrophages, facilitating the M1-to-M2 transition and the recovery of associated cytokines and biomarkers to the normal level. The therapeutic efficacy of FA-tDONs was examined in the RA mouse model. As validated by appearance, histological, and serum examinations, FA-tDONs treatment effectively alleviated synovial infiltration and cartilage damage, attenuating disease progression. This study demonstrated the usage of DNA origami for RA treatment and suggested its potential in other antioxidant therapies.
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