Tian Jialu, Zhang Lixia, Qiao Yanchun, Yang Jie, Mengji Rakesh, Lee Yubin, Hong Seokjin, Duan Yu, Zhou Xucong, Kim Jong Seung, Zhou Jin
Affiliated Hospital of Shandong Second Medical University (261031, School of Clinical Medicine), School of Pharmacy, Shandong Second Medical University, Weifang 261053, People's Republic of China.
Department of Chemistry, Korea University, Seoul 02841, South Korea.
Anal Chem. 2025 Jul 22;97(28):15244-15252. doi: 10.1021/acs.analchem.5c01887. Epub 2025 Jul 8.
Early cancer diagnosis greatly enhances survival rates and improves patients' quality of life. Intracellular viscosity, among various microenvironmental factors influencing cellular function, plays a pivotal role. Abnormal viscosity levels are closely linked to cancer progression, impacting biomolecular diffusion, metabolic activity, and signal transduction. Monitoring and understanding changes in intracellular viscosity could offer valuable insights into early cancer detection and therapeutic strategies. Notably, increased mitochondrial viscosity is associated with malignant tumor development. Since mitochondria play a key role in cancer, studying their function, especially in mitophagy (mitochondrial recycling) and apoptosis (programmed cell death), is crucial for cancer research and treatment. Herein, we report a fluorescent probe with large Stokes shifts designed for mitochondrial viscosity imaging. The probe features an indolium iodide moiety for enhanced mitochondrial targeting and a 2-chlorocyclohex-1-ene-1-carbaldehyde group to extend emission wavelengths. exhibits a viscosity-dependent fluorescence turn-on at 635 nm, with a linear response ranging from 0.89 to 945 cP. Using , we successfully monitored mitochondrial viscosity changes in live cells under LPS, OA, and nystatin treatment. Furthermore, the probe enabled real-time imaging of mitochondrial viscosity variations during mitophagy (starvation-induced) and apoptosis (cisplatin-induced) at the cellular level. Meanwhile, successfully detected dynamic fluctuations of viscosity in zebrafish animal models. Importantly, revealed elevated mitochondrial viscosity in tumor tissues compared with normal tissues. Furthermore, it enabled dynamic monitoring of therapeutic responses, highlighting its potential as a powerful tool for evaluating cancer treatment efficacy.
早期癌症诊断可显著提高生存率并改善患者生活质量。在影响细胞功能的各种微环境因素中,细胞内粘度起着关键作用。异常的粘度水平与癌症进展密切相关,影响生物分子扩散、代谢活性和信号转导。监测和了解细胞内粘度的变化可为早期癌症检测和治疗策略提供有价值的见解。值得注意的是,线粒体粘度增加与恶性肿瘤发展有关。由于线粒体在癌症中起关键作用,研究其功能,特别是在细胞自噬(线粒体循环利用)和细胞凋亡(程序性细胞死亡)中的功能,对癌症研究和治疗至关重要。在此,我们报告了一种用于线粒体粘度成像的具有大斯托克斯位移的荧光探针。该探针具有碘化吲哚部分以增强线粒体靶向性,以及2-氯环己-1-烯-1-甲醛基团以延长发射波长。在635nm处表现出粘度依赖性荧光开启,线性响应范围为0.89至945厘泊。使用该探针,我们成功监测了脂多糖、油酸和制霉菌素处理下活细胞中线粒体粘度的变化。此外,该探针能够在细胞水平实时成像细胞自噬(饥饿诱导)和细胞凋亡(顺铂诱导)过程中线粒体粘度的变化。同时,该探针成功检测了斑马鱼动物模型中粘度的动态波动。重要的是,该探针显示肿瘤组织中的线粒体粘度高于正常组织。此外,它能够动态监测治疗反应,突出了其作为评估癌症治疗效果的强大工具的潜力。