Multiparameter Assessment of Foam Cell Formation Progression Using a Dual-Color Switchable Fluorescence Probe

• Published in: Analytical chemistry (Washington) 2024-05, Vol.96 (18), p.6968-6977
• Main Authors: Li, Zi-Lu, Han, Gui-Mei, Wang, Kun, Lyu, Jia-Ao, Li, Zi-Wen, Zhu, Bao-Cun, Zhu, Li-Na, Kong, De-Ming
• Format: Article
• Language: English
• Subjects: Animals; Arteriosclerosis; Atherosclerosis; Atherosclerosis - diagnostic imaging; Atherosclerosis - metabolism; Atherosclerosis - pathology; Color; Fluorescent Dyes - chemistry; Fluorescent indicators; Foam Cells - metabolism; Foam Cells - pathology; Humans; Hydrogen-Ion Concentration; Imaging; Lipid Droplets - chemistry; Lipid Droplets - metabolism; Lipid metabolism; Lipids; Lysosomes; Lysosomes - metabolism; Mice; Molecular structure; Monitoring; Optical Imaging; Pharmacokinetics; RAW 264.7 Cells
• ISSN: 0003-2700; 1520-6882; 1520-6882
• DOI: 10.1021/acs.analchem.3c05940

The assessment of atherosclerosis (AS) progression has emerged as a prominent area of research. Monitoring various pathological features of foam cell (FC) formation is imperative to comprehensively assess AS progression. Herein, a simple benzospiropyran-julolidine-based probe, BSJD, with switchable dual-color imaging ability was developed. This probe can dynamically and reversibly adjust its molecular structure and fluorescent properties in different polar and pH environments. Such a polarity and pH dual-responsive characteristic makes it superior to single-responsive probes in dual-color imaging of lipid droplets (LDs) and lysosomes as well as monitoring their interaction. By simultaneously tracking various pathological features, including LD accumulation and size changes, lysosome dysfunction, and dynamically regulated lipophagy, more comprehensive information can be obtained for multiparameter assessment of FC formation progression. Using BSJD, not only the activation of lipophagy in the early stages and inhibition in the later phases during FC formation are clearly observed but also the important roles of lipophagy in regulating lipid metabolism and alleviating FC formation are demonstrated. Furthermore, BSJD is demonstrated to be capable of rapidly imaging FC plaque sites in AS mice with fast pharmacokinetics. Altogether, BSJD holds great promise as a dual-color organelle-imaging tool for investigating disease-related LD and lysosome changes and their interactions.