Fan Li, Yang Qianqian, Zan Qi, Zhao Kunyi, Lu Wenjing, Wang Xu, Wang Yu, Shuang Shaomin, Dong Chuan
Institute of Environmental Science, College of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, P. R. China.
Shanxi Research Center for Information and Strategy of Science and Technology, Taiyuan 030024, P. R. China.
Anal Chem. 2023 Apr 4;95(13):5780-5787. doi: 10.1021/acs.analchem.3c00142. Epub 2023 Mar 20.
Intracellular peroxynitrite anions (ONOO) and microenvironments (such as viscosity and polarity) play an important role in maintaining redox homeostasis, regulating diffusion, transportation, and signal transduction in living cells. The abnormality of these factors is often closely related to various physiological/pathological processes. However, owing to the lack of suitable probes, the simultaneous visualization of ONOO, viscosity, and polarity in ferroptosis and cancer models has not been achieved. To meet urgent needs, we presented a multifunctional near-infrared (NIR) fluorescent probe, named , for simultaneously detecting ONOO, viscosity, and polarity within mitochondria. The probe exhibited a remarkable turn-on response to ONOO with the far-red emission of about 645 nm and was highly sensitive to viscosity/polarity in the NIR channel with λ > 704 nm. Facilitated by , for the first time, we revealed that erastin-induced ferroptosis was accompanied by a significant upregulation of ONOO and an increase of viscosity (or decrease of polarity) at the same time. Moreover, the concurrent use of ONOO, viscosity, and polarity for the diagnosis of cancer has been successfully achieved not only at cell/tissue levels but also in tumor mice models. Compared with detecting only one factor, this simultaneous detection of multimarkers provides a more sensitive and reliable method/tool for tracking ferroptosis-related pathological processes and cancer diagnosis, holding great potential in preclinical research, medical diagnosis, and imaging-guided surgery.
细胞内过氧亚硝酸根阴离子(ONOO⁻)和微环境(如粘度和极性)在维持氧化还原稳态、调节活细胞中的扩散、运输和信号转导方面发挥着重要作用。这些因素的异常通常与各种生理/病理过程密切相关。然而,由于缺乏合适的探针,尚未实现对铁死亡和癌症模型中ONOO⁻、粘度和极性的同时可视化。为满足迫切需求,我们提出了一种多功能近红外(NIR)荧光探针,名为 ,用于同时检测线粒体内的ONOO⁻、粘度和极性。该探针对ONOO⁻表现出显著的开启响应,发出约645 nm的远红光,并且在λ>704 nm的近红外通道中对粘度/极性高度敏感。借助 ,我们首次揭示了埃拉司亭诱导的铁死亡伴随着ONOO⁻的显著上调以及粘度的增加(或极性的降低)。此外,不仅在细胞/组织水平,而且在肿瘤小鼠模型中,已成功实现同时使用ONOO⁻、粘度和极性进行癌症诊断。与仅检测一个因素相比,这种多标志物的同时检测为跟踪铁死亡相关的病理过程和癌症诊断提供了一种更灵敏、可靠的方法/工具,在临床前研究、医学诊断和影像引导手术中具有巨大潜力。