State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials Oriented Chemical Engineering, Dalian University of Technology, Dalian 116024, China.
J Am Chem Soc. 2023 Dec 27;145(51):28296-28306. doi: 10.1021/jacs.3c12181. Epub 2023 Dec 13.
Atherosclerosis (AS) is the formation of plaques in blood vessels, which leads to serious cardiovascular diseases. Current research has disclosed that the formation of AS plaques is highly related to the foaming of macrophages. However, there is a lack of detailed molecular biological mechanisms. We proposed a "live sensor" by grafting a tetrazine-based ratiometric NO probe within macrophages through metabolic and bio-orthogonal labeling. This "live sensor" was proved to target the AS plaques with a diameter of only tens of micrometers specifically and visualized endogenous NO at two lesion stages in the AS mouse model. The ratiometric signals from the probe confirmed the participation of NO during AS and indicated that the generation of endogenous NO increased significantly as the lesion progressed. Our proposal of this "live sensor" provided a native and smart strategy to target and deliver small molecular probes to the AS plaques at the in vivo level, which can be used as universal platforms for the detection of reactive molecules or microenvironmental factors in AS.
动脉粥样硬化(AS)是血管中斑块的形成,可导致严重的心血管疾病。目前的研究表明,AS 斑块的形成与巨噬细胞的泡沫化密切相关,但缺乏详细的分子生物学机制。我们通过代谢和生物正交标记将基于四嗪的比率型 NO 探针嫁接到巨噬细胞中,提出了一种“活体传感器”。该“活体传感器”被证明可以特异性地靶向直径仅数十微米的 AS 斑块,并在 AS 小鼠模型的两个病变阶段可视化内源性 NO。探针的比率信号证实了 NO 在 AS 中的参与,并表明随着病变的进展,内源性 NO 的产生显著增加。我们提出的这种“活体传感器”为在体内水平上将小分子探针靶向和递送至 AS 斑块提供了一种原生和智能的策略,可作为用于检测 AS 中反应性分子或微环境因素的通用平台。