Koo Seyoung, Won Miae, Li Hao, Kim Won Young, Li Mingle, Yan Chenxu, Sharma Amit, Guo Zhiqian, Zhu Wei-Hong, Sessler Jonathan L, Lee Jin Yong, Kim Jong Seung
Department of Chemistry, Korea University Seoul 02841 Korea
Department of Chemistry, Sungkyunkwan University Suwon 16419 Korea.
Chem Sci. 2021 Jun 25;12(29):10054-10062. doi: 10.1039/d1sc02259h. eCollection 2021 Jul 28.
Precise detection of cellular senescence may allow its role in biological systems to be evaluated more effectively, while supporting studies of therapeutic candidates designed to evade its detrimental effect on physical function. We report here studies of α-l-fucosidase (α-fuc) as a biomarker for cellular senescence and the development of an α-fuc-responsive aggregation induced emission (AIE) probe, termed designed to complement more conventional probes based on β-galactosidase (β-gal). Using , the onset of replicative-, reactive oxygen species (ROS)-, ultraviolet A (UVA)-, and drug-induced senescence could be probed effectively. also proved capable of identifying senescent cells lacking β-gal expression. The non-invasive real-time senescence tracking provided by was validated in an senescence model. The results presented in this study lead us to suggest that the could emerge as a useful tool for investigating senescence processes in biological systems.
精确检测细胞衰老可能有助于更有效地评估其在生物系统中的作用,同时支持对旨在规避其对身体功能有害影响的候选治疗方法的研究。我们在此报告了对α-L-岩藻糖苷酶(α-fuc)作为细胞衰老生物标志物的研究,以及一种α-fuc响应性聚集诱导发光(AIE)探针的开发,该探针旨在补充基于β-半乳糖苷酶(β-gal)的更传统探针。使用该探针,可以有效地探测复制性、活性氧(ROS)、紫外线A(UVA)和药物诱导的衰老的起始。该探针还能够识别缺乏β-gal表达的衰老细胞。该探针提供的非侵入性实时衰老追踪在体内衰老模型中得到了验证。本研究结果使我们认为,该探针可能成为研究生物系统中衰老过程的有用工具。