化学
过氧亚硝酸盐
纳米探针
CD36
荧光
氧化应激
下调和上调
生物物理学
细胞生物学
生物化学
染色
免疫荧光
荧光寿命成像显微镜
荧光染色
细胞衰老
分子生物学
体外
淀粉样蛋白(真菌学)
作者
Xiaoyu Gu,Yue Li,Xin Xia,Wei Zhang,Wei Zhang,Ping Li,Wei Zhang,Wei Zhang,H Z Wang,Bo Tang
标识
DOI:10.1021/acs.analchem.6c02314
摘要
The vicious cycle of oxidative stress and cellular senescence is closely associated with the development and progression of atherosclerosis. Targeting the vicious cycle of “oxidative stress-cell senescence” as a combined biological target for atherosclerosis and developing dual-functional probes holds significant importance for the early monitoring and risk assessment of this disease. Therefore, fluorescent nanoprobe GL-1-NPs, capable of simultaneously imaging the aging markers β-galactosidase (β-gal) and peroxynitrite (ONOO – ) were synthesized via nanoprecipitation. GL-1-NPs serve as a live-cell imaging tool that enables effective monitoring of changes in β-gal activity and ONOO – levels during the formation process of foam cells. Notably, in the aortas of ApoE –/– mice fed a high-fat diet for 12 weeks, traditional methods such as Oil Red O staining and immunofluorescence revealed no plaque formation or upregulation of the associated proteins CD36 and CD68. Whereas, GL-1-NPs successfully detected enhanced fluorescence signals in the β-gal and ONOO – channels, highlighting their potential for achieving early warning of atherosclerosis.
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