荧光团
体内
荧光
糖苷键
基质(水族馆)
化学
酶
生物化学
细胞生物学
生物物理学
生物
生态学
量子力学
物理
生物技术
作者
Sara Rojas-Vázquez,Beatriz Lozano‐Torres,Alba García‐Fernández,Irene Galiana,Ana Pérez‐Villalba,Pablo Martí‐Rodrigo,M. José Palop,Marcia Domínguez,Mar Orzáez,Félix Sancenón,Juan F. Blandez,Isabel Fariñas,Ramón Martı́nez-Máñez
标识
DOI:10.1038/s41467-024-44903-1
摘要
Abstract Accumulation of senescent cells with age leads to tissue dysfunction and related diseases. Their detection in vivo still constitutes a challenge in aging research. We describe the generation of a fluorogenic probe (sulfonic-Cy7Gal) based on a galactose derivative, to serve as substrate for β-galactosidase, conjugated to a Cy7 fluorophore modified with sulfonic groups to enhance its ability to diffuse. When administered to male or female mice, β-galactosidase cleaves the O-glycosidic bond, releasing the fluorophore that is ultimately excreted by the kidneys and can be measured in urine. The intensity of the recovered fluorophore reliably reflects an experimentally controlled load of cellular senescence and correlates with age-associated anxiety during aging and senolytic treatment. Interestingly, our findings with the probe indicate that the effects of senolysis are temporary if the treatment is discontinued. Our strategy may serve as a basis for developing fluorogenic platforms designed for easy longitudinal monitoring of enzymatic activities in biofluids.
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