内化
中性粒细胞胞外陷阱
活性氧
普鲁士蓝
化学
细胞内
炎症
癌症研究
细胞生物学
医学
免疫学
生物
细胞
生物化学
电极
物理化学
电化学
作者
Ming Wu,Mengjuan Chen,Yuzhen Zhao,Xijun Zhang,Xiao Ding,Jianjun Yuan,Jinjin Shi,Wenyan Yu,Haohui Zhu
标识
DOI:10.1002/smtd.202402019
摘要
Abstract Atherosclerosis (AS), a chronic inflammatory disease and a leading cause of cardiovascular morbidity and mortality worldwide, is a significant contributor to disability. Neutrophil extracellular traps (NETs) have been closely associated with the progression of AS and plaque vulnerability. However, developing a treatment strategy that specifically targets neutrophils and effectively reduces NET release at the lesion site remains a major challenge. In this study, a biomimetic nanosystem with neutrophil‐targeting properties is engineered. Coating Prussian blue nanoparticles with bacterial biomimetic membranes (MPB NPs) enables specific recognition and internalization by neutrophils. By hitching onto neutrophils, the MPB NPs scavenge intracellular reactive oxygen species (ROS) and suppress NET formation at the lesion site. Importantly, MPB NPs reduce the size of atherosclerotic plaques by 3.29‐fold, from 22.53% to 6.85%, stabilize the plaques, and halt their progression in atherosclerotic mouse models. These findings suggest that MPB NPs offer a promising therapeutic strategy for atherosclerosis, and provide a versatile platform for the treatment of NET‐associated diseases.
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