Division of Cellular Senescence, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.
Department of JFCR Cancer Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Cancer Sci. 2024 Aug;115(8):2762-2773. doi: 10.1111/cas.16229. Epub 2024 May 27.
Senescent cells promote cancer development and progression through chronic inflammation caused by a senescence-associated secretory phenotype (SASP). Although various senotherapeutic strategies targeting senescent cells have been developed for the prevention and treatment of cancers, technology for the in vivo detection and evaluation of senescent cell accumulation has not yet been established. Here, we identified activatable fluorescent probes targeting dipeptidylpeptidase-4 (DPP4) as an effective probe for detecting senescent cells through an enzymatic activity-based screening of fluorescent probes. We also determined that these probes were highly, selectively, and rapidly activated in senescent cells during live cell imaging. Furthermore, we successfully visualized senescent cells in the organs of mice using DPP4-targeted probes. These results are expected to lead to the development of a diagnostic technology for noninvasively detecting senescent cells in vivo and could play a role in the application of DPP4 prodrugs for senotherapy.
衰老细胞通过衰老相关分泌表型(SASP)引起的慢性炎症促进癌症的发生和发展。尽管已经开发了各种针对衰老细胞的衰老治疗策略来预防和治疗癌症,但尚未建立用于体内检测和评估衰老细胞积累的技术。在这里,我们通过荧光探针的基于酶活性的筛选,鉴定了靶向二肽基肽酶-4(DPP4)的激活型荧光探针,作为一种有效的检测衰老细胞的探针。我们还确定,在活细胞成像过程中,这些探针在衰老细胞中高度、选择性和快速地被激活。此外,我们还成功地使用 DPP4 靶向探针在小鼠的器官中可视化衰老细胞。这些结果有望为开发非侵入性体内检测衰老细胞的诊断技术铺平道路,并可能为 DPP4 前药在衰老治疗中的应用提供帮助。