Multimodal Imaging-Assisted Intravascular Theranostic Photoactivation on Atherosclerotic Plaque

炎症 传出细胞增多 梅尔特克 光动力疗法 病理 癌症研究 体内 化学 巨噬细胞 医学 细胞生物学 免疫学 生物 受体酪氨酸激酶 生物化学 受体 体外 有机化学 生物技术
作者
Jin Hyuk Kim,Joon Woo Song,Yeon Hoon Kim,Hyun Jung Kim,Ryeong Hyun Kim,Ye Hee Park,Hyeong Soo Nam,Dong Oh Kang,Hongki Yoo,Kyeongsoon Park,Jin Won Kim,Jin Won Kim,Jin Won Kim
出处
期刊:Circulation Research [Lippincott Williams & Wilkins]
卷期号:135 (5): e114-e132 被引量:5
标识
DOI:10.1161/circresaha.123.323970
摘要

BACKGROUND: Atherosclerosis is a chronic inflammatory disease causing a fatal plaque rupture, and its key aspect is a failure to resolve inflammation. We hypothesize that macrophage-targeted near-infrared fluorescence emitting photoactivation could simultaneously assess macrophage/lipid-rich plaques in vivo and facilitate inflammation resolution. METHODS: We fabricated a Dectin-1–targeted photoactivatable theranostic agent through the chemical conjugation of the near-infrared fluorescence–emitting photosensitizer chlorin e6 and the Dectin-1 ligand laminarin (laminarin-chlorin e6 [LAM-Ce6]). Intravascular photoactivation by a customized fiber-based diffuser after administration of LAM-Ce6 effectively reduced inflammation in the targeted plaques of atherosclerotic rabbits in vivo as serially assessed by dual-modal optical coherence tomography-near-infrared fluorescence structural-molecular catheter imaging after 4 weeks. RESULTS: The number of apoptotic macrophages peaked at 1 day after laser irradiation and then resolved until 4 weeks. Autophagy was strongly augmented 1 hour after the light therapy, with the formation of autophagolysosomes. LAM-Ce6 photoactivation increased the terminal deoxynucleotidyl transferase dUTP (deoxyuridine triphosphate) nick end labeling/RAM11 (rabbit monocyte/macrophage antibody)- and MerTK (c-Mer tyrosine kinase)-positive cells in the plaques, suggesting enhanced efferocytosis. In line with inflammation resolution, photoactivation reduced the plaque burden through fibrotic replacement via the TGF (transforming growth factor)-β/CTGF (connective tissue growth factor) pathway. CONCLUSIONS: Optical coherence tomography-near-infrared fluorescence imaging-guided macrophage Dectin-1–targetable photoactivation could induce the transition of macrophage/lipid-rich plaques into collagen-rich lesions through autophagy-mediated inflammation resolution and TGF-β–dependent fibrotic replacement. This novel strategy offers a new opportunity for the catheter-based theranostic strategy.
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