Xue Huanxin, Wang Xueli, Jiang Qiuyan, Ma Jiale, Wong Man Shing
Department of Chemistry, Hong Kong Baptist University, Kowloon Tong, Hong Kong Special Administrative Region of China.
College of Pharmaceutical Sciences, College of Chemistry & Environmental Science, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis, Ministry of Education, Hebei University, Baoding, 071002, China.
Biosens Bioelectron. 2025 May 1;275:117201. doi: 10.1016/j.bios.2025.117201. Epub 2025 Jan 28.
Amyloid-β (Aβ), the hallmark of Alzheimer's disease (AD), is known to induce reactive oxygen species, peroxynitrite (ONOO) which plays a crucial role in the pathogenesis and progression of this incurable disease. However, the development of tools that can directly detect the presence and monitor the level of Aβ-induced ONOO remains a great challenge. We report herein the development of an Aβ and ONOO synergistically activated NIR fluorescent probe for highly selective imaging of Aβ-induced ONOO level in vivo. Importantly, this responsive probe exhibits not only synergistically strong enhancement of fluorescence at 655 nm upon reacting with ONOO in the presence of Aβ but also high sensitivity down to 13 nM with minimal interference. The strong Aβ binding and low cytotoxicity enable the probe to successfully apply for detecting and visualizing endogenous ONOO level induced by Aβ in AD cell model. Remarkably, this ONOO-responsive probe can be applied effectively to detect, monitor, and distinguish varying ONOO levels induced by Aβ in different age groups of AD mice, in which cerebral ONOO level rises with increasing age of AD mice along with Aβ plaque accumulation. Furthermore, the potent neuroprotection against Aβ-induced toxicity and anti-Aβ aggregation effect of the ONOO-reaction product of the probe offer an extra therapeutic advantage of this ONOO-responsive probe. In essence, this multifunctional theranostic probe can serve as a highly sensitive and specific imaging tool for visualizing and monitoring of ONOO level in the presence of Aβ in vivo, thereby facilitating more accurate early diagnosis and therapy of AD.
淀粉样β蛋白(Aβ)是阿尔茨海默病(AD)的标志,已知其可诱导活性氧、过氧亚硝酸盐(ONOO),而过氧亚硝酸盐在这种不治之症的发病机制和进展中起着关键作用。然而,开发能够直接检测Aβ诱导的ONOO的存在并监测其水平的工具仍然是一个巨大的挑战。我们在此报告了一种Aβ和ONOO协同激活的近红外荧光探针的开发,用于在体内对Aβ诱导的ONOO水平进行高选择性成像。重要的是,这种响应性探针不仅在与Aβ存在下的ONOO反应时在655nm处表现出荧光的协同强烈增强,而且具有低至13 nM的高灵敏度且干扰最小。强大的Aβ结合能力和低细胞毒性使该探针能够成功应用于检测和可视化AD细胞模型中Aβ诱导的内源性ONOO水平。值得注意的是,这种对ONOO响应的探针可以有效地应用于检测、监测和区分不同年龄组的AD小鼠中Aβ诱导的不同ONOO水平,其中随着AD小鼠年龄的增加以及Aβ斑块的积累,脑内ONOO水平升高。此外,该探针的ONOO反应产物对Aβ诱导的毒性具有强大的神经保护作用和抗Aβ聚集作用,为这种对ONOO响应的探针提供了额外的治疗优势。本质上,这种多功能诊疗探针可以作为一种高灵敏度和特异性的成像工具,用于在体内可视化和监测Aβ存在下的ONOO水平,从而有助于更准确地早期诊断和治疗AD。