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J Med Chem ; 67(14): 12428-12438, 2024 Jul 25.
Article in English | MEDLINE | ID: mdl-38996002

ABSTRACT

Targeting Ca2+/calmodulin-dependent protein kinase γ (CaMKIIγ) in macrophages using RNAi nanotechnology represents an innovative and promising strategy in the diagnosis and treatment of atherosclerosis. Nevertheless, it remains elusive because of the current challenges associated with the systemic delivery of siRNA nanoparticle (NP) to atheromatous plaques and the complexity of atherosclerotic plaques. Here, we demonstrate the potential of a thienothiadiazole-based near-infrared-II (NIR-II) organic aggregation-induced emission (AIE) platform encapsulated with the Camk2g siRNA to effectively target CaMKIIγ in macrophages for dynamic imaging and image-guided gene therapy of atherosclerosis. The nanoparticles effectively decreased CaMKIIγ expression and increased the expression of the efferocytosis receptor MerTK in plaque macrophages, leading to a reduction in the necrotic core area of the lesion in an aortic plaque model. Our theranostic approach highlights the substantial promise of near-infrared II (NIR-II) AIEgens for imaging and image-guided therapy of atherosclerosis.


Subject(s)
Atherosclerosis , Optical Imaging , RNA, Small Interfering , Animals , Humans , Mice , Atherosclerosis/diagnostic imaging , Atherosclerosis/therapy , Infrared Rays , Macrophages/metabolism , Mice, Inbred C57BL , Nanoparticles/chemistry , Plaque, Atherosclerotic/diagnostic imaging , RNA, Small Interfering/chemistry , RNA, Small Interfering/therapeutic use , Thiadiazoles/chemistry , Thiadiazoles/pharmacology , Calcium-Calmodulin-Dependent Protein Kinases/chemistry , Calcium-Calmodulin-Dependent Protein Kinases/metabolism
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