Jaeger Sophia, Lanquaye Henry, Dwivedi Sushil K, Arachchige Dilka Liyana, Xia James, Waters May, Bigari Bella Lyn, Olowolagba Adenike Mary, Agyemang Peter, Zhang Yang, Zhang Yan, Ata Athar, Kathuria Ishana, Luck Rudy L, Werner Thomas, Liu Haiying
Department of Chemistry, Michigan Technological University, Houghton, Michigan 49931, United States.
Health Research Institute, Michigan Technological University, Houghton, Michigan 49931, United States.
ACS Appl Bio Mater. 2024 Dec 16;7(12):8465-8478. doi: 10.1021/acsabm.4c01294. Epub 2024 Nov 19.
A near-infrared fluorescent probe, , was designed by substituting the carbonyl group of the coumarin dye's lactone with a 4-cyano-1-methylpyridinium methylene group and then attaching an electron-withdrawing NADH-sensing methylquinolinium acceptor via a vinyl bond linkage to the coumarin dye at the 4-position. The probe exhibits primary absorption maxima at 603, 428, and 361 nm, and fluoresces weakly at 703 nm. The addition of NAD(P)H results in a significant blue shift in the fluorescence peak from 703 to 670 nm, accompanied by a substantial increase in fluorescence intensity. This spectral shift is attributed to the transformation from an A-π-A-π-D configuration to a D-π-A-π-D pyridinium platform in probe , owing to the addition of a hydride from NADH to the electron-accepting quinolinium acceptor producing the electron-contributing 1-methyl-1,4-dihydroquinoline donor in probe . This conclusion is supported by theoretical calculations. The probe was utilized to investigate NAD(P)H dynamics under various conditions. In HeLa cells, treatment with glucose or maltose resulted in a substantial elevation in near-infrared emission intensity, suggesting increased NAD(P)H levels. Chemotherapeutic agents including cisplatin and fludarabine at concentrations of 5, 10, and 20 μM brought about a dose-dependent increase in emission intensity, reflecting heightened NAD(P)H levels due to drug-induced stress and cellular damage. In vivo experiments with hatched, starved larvae were also conducted. The results showed a clear relationship between emission intensity and the levels of NADH, glucose, and oxaliplatin, confirming that the probe can detect variations in NAD(P)H levels in a living organism. Our investigation also demonstrates that NAD(P)H levels are significantly elevated in the cystic kidneys of ADPKD mouse models and human patients, indicating substantial metabolic alterations associated with the disease. This near-infrared emissive probe offers a highly sensitive and specific method for monitoring NAD(P)H levels across cellular, tissue and whole-organism systems. The ability to detect NAD(P)H variations in reaction to varying stimuli, including nutrient availability and chemotherapeutic stress, underscores its potential as a valuable resource for biomedical research and therapeutic monitoring.
一种近红外荧光探针,通过用4-氰基-1-甲基吡啶亚甲基取代香豆素染料内酯的羰基,然后通过乙烯基键连接在4位将吸电子的NADH传感甲基喹啉受体连接到香豆素染料上而设计。该探针在603、428和361nm处有主要吸收峰,在703nm处微弱发光。加入NAD(P)H会导致荧光峰从703nm显著蓝移至670nm,同时荧光强度大幅增加。这种光谱位移归因于探针中从A-π-A-π-D构型转变为D-π-A-π-D吡啶鎓平台,这是由于NADH中的氢化物添加到吸电子的喹啉受体上,在探针中产生了提供电子的1-甲基-1,4-二氢喹啉供体。这一结论得到了理论计算的支持。该探针用于研究各种条件下的NAD(P)H动力学。在HeLa细胞中,用葡萄糖或麦芽糖处理导致近红外发射强度大幅升高,表明NAD(P)H水平增加。浓度为5、10和20μM的顺铂和氟达拉滨等化疗药物导致发射强度呈剂量依赖性增加,反映出由于药物诱导的应激和细胞损伤导致NAD(P)H水平升高。还对孵化后饥饿的幼虫进行了体内实验。结果表明发射强度与NADH、葡萄糖和奥沙利铂水平之间存在明显关系,证实该探针可以检测活生物体中NAD(P)H水平的变化。我们的研究还表明,在常染色体显性多囊肾病小鼠模型和人类患者的多囊肾中,NAD(P)H水平显著升高,表明与该疾病相关的大量代谢改变。这种近红外发射探针为监测细胞、组织和全生物体系统中的NAD(P)H水平提供了一种高度灵敏和特异的方法。能够检测对包括营养可用性和化疗应激在内的不同刺激作出反应的NAD(P)H变化,突出了其作为生物医学研究和治疗监测宝贵资源的潜力。