化学
三磷酸腺苷
线粒体
一氧化氮
脂多糖
氧化应激
细胞生物学
柠檬酸循环
肺
氧化磷酸化
平衡
药理学
转录组
糖酵解
生物化学
腺苷
活性氧
生物物理学
ATP合酶
呼吸
新陈代谢
细胞呼吸
嘌呤能受体
膜电位
荧光寿命成像显微镜
炎症
缺氧(环境)
代谢组学
药品
细胞代谢
作者
Xinyue Li,Jinzhen Zheng,Ning Li,Pu Sun,Zhiang Duan,Wenyuan Cheng,Wenting Guo,Baodui Wang
标识
DOI:10.1021/acs.analchem.6c00236
摘要
Acute lung injury (ALI) involves severe mitochondrial dysfunction, where the dynamic interplay between nitric oxide (NO) and adenosine triphosphate (ATP) remains elusive due to the lack of tools for their simultaneous visualization. Here, we developed ANRC, an orthogonal near-infrared (NIR) and mitochondria-targeted fluorescent probe that enabled ratiometric imaging of NO and turn-on detection of ATP in live cells and in vivo. ANRC exhibited high selectivity, with a linear response to ATP in the 0.5–8 mM range and to NO in the 0–40 μM range, and detection limits of 1.3 μM for ATP and 0.26 μM for NO. In a lipopolysaccharide (LPS)-induced ALI model, ANRC visualized a metabolic imbalance characterized by elevated NO and depleted ATP. Transcriptomic analysis revealed that NO disrupted mitochondrial respiration and the tricarboxylic acid (TCA) cycle, impairing ATP synthesis. Using ANRC as a screening tool, we identified dexmedetomidine (DEX) as a therapeutic candidate that restored NO/ATP homeostasis and alleviated lung injury. This work presents a powerful dual-analyte imaging platform for studying mitochondrial metabolism and oxidative stress in ALI, offering new opportunities for diagnosis and drug development.
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