Why the study?
Does treatment with Prussian blue nanoparticles coated with bacterial biomimetic membranes (MPB NPs) reduce atherosclerotic plaque size in atherosclerotic mouse models?
Does treatment with Prussian blue nanoparticles coated with bacterial biomimetic membranes (MPB NPs) reduce atherosclerotic plaque size in atherosclerotic mouse models?
Neutrophil-targeted biomimetic nanoparticles (MPB NPs) significantly reduce atherosclerotic plaque size and stabilize plaques in mouse models by scavenging ROS and suppressing NET formation.
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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Wu et al. (2025) studied Atherosclerosis. Bacterial biomimetic membrane-coated Prussian blue nanoparticles (MPB NPs) was evaluated on Atherosclerotic plaque size (3.29-fold reduction).
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