A Spatially Cued, Sequentially Activated DNA Nanodevice for Atherosclerosis Theranostics via Precise Targeting of
Ping Xie1, Xumin Pan1, Ruixi Peng1
1State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, P. R. China.
Abstract:
Atherosclerosis (AS), a major contributor to cardiovascular diseases, involves macrophages as a pivotal driver of its pathogenesis. Developing macrophage-targeted therapies that effectively mitigate AS while minimizing systemic effects remains a challenge. Here, we present an intelligent theranostic method for AS using an accurate spatiotemporal-specifically responsive DNA nanostructure (ASfindaCure). To precisely target atherogenic macrophages, we leverage a spatially distinctive expression pattern comprising a membrane protein (SIRPα), a microenvironmental cue (thrombin), and two intracellular biomarkers (APE1 and microRNA-155). By harnessing structural and dynamic DNA nanotechnologies, ASfindaCure temporally orchestrates recognition events for these spatially distributed biomarkers via programmable reaction cascades. Utilizing fluorescence and photoacoustic dual-modality imaging, we demonstrate that ASfindaCure accurately targets AS-causing macrophages, providing a noninvasive imaging method to assess AS progression. In both cellular and mouse models, ASfindaCure demonstrated effective delivery of microRNA-33 antisense oligonucleotides to targeted cells, significantly mitigating plaque progression and inflammation. This intelligent theranostic nanoplatform holds great promise for the development of next-generation treatments for AS and has potential applications in other disease conditions.
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