AI Article Synopsis

  • Senescent cells accumulate with age, leading to tissue dysfunction and diseases, making their detection challenging in aging research.
  • The study introduces a new fluorogenic probe (sulfonic-Cy7Gal) that helps detect cellular senescence by releasing a measurable fluorophore after being cleaved by β-galactosidase in mice.
  • The probe's effectiveness is shown to correlate with age-related anxiety and the temporary effects of senolytic treatment, suggesting it could be used for ongoing monitoring of enzymatic activities related to aging.

Article 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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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10817927PMC
http://dx.doi.org/10.1038/s41467-024-44903-1DOI Listing

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