1. Academic Validation
  2. A Glb1-2A-mCherry reporter monitors systemic aging and predicts lifespan in middle-aged mice

A Glb1-2A-mCherry reporter monitors systemic aging and predicts lifespan in middle-aged mice

  • Nat Commun. 2022 Nov 17;13(1):7028. doi: 10.1038/s41467-022-34801-9.
Jie Sun # 1 2 3 Ming Wang # 1 2 Yaqi Zhong # 1 Xuan Ma 1 Shimin Sun 1 Chenzhong Xu 1 2 Linyuan Peng 1 Guo Li 4 Liting Zhang 1 Zuojun Liu 1 2 Ding Ai 5 Baohua Liu 6 7 8
Affiliations

Affiliations

  • 1 Shenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, 518055, China.
  • 2 Guangdong Key Laboratory of Genome Stability and Human Disease Prevention, Marshall Laboratory of Biomedical Engineering, National Engineering Research Center for Biotechnology (Shenzhen), International Cancer Center, Shenzhen University, Shenzhen, 518055, China.
  • 3 Shenzhen Bay Laboratory, Shenzhen, China.
  • 4 Department of Dermatology, Xiangya Hospital, Central South University, Changsha, China.
  • 5 Department of Physiology and Pathophysiology, Tianjin Medical University, Tianjin, 300070, China.
  • 6 Shenzhen Key Laboratory for Systemic Aging and Intervention (SKL-SAI), School of Basic Medical Sciences, Shenzhen University, Shenzhen, 518055, China. [email protected].
  • 7 Guangdong Key Laboratory of Genome Stability and Human Disease Prevention, Marshall Laboratory of Biomedical Engineering, National Engineering Research Center for Biotechnology (Shenzhen), International Cancer Center, Shenzhen University, Shenzhen, 518055, China. [email protected].
  • 8 Shenzhen Bay Laboratory, Shenzhen, China. [email protected].
  • # Contributed equally.
Abstract

The progressive decline of physiological function and the increased risk of age-related diseases challenge healthy aging. Multiple Anti-aging manipulations, such as senolytics, have proven beneficial for health; however, the biomarkers that label in vivo senescence at systemic levels are lacking, thus hindering Anti-aging applications. In this study, we generate a Glb1+/m‒Glb1-2A-mCherry (GAC) reporter allele at the Glb1 gene locus, which encodes lysosomal β-galactosidase-an enzyme elevated in tissues of old mice. A linear correlation between GAC signal and chronological age is established in a cohort of middle-aged (9 to 13 months) Glb1+/m mice. The high GAC signal is closely associated with cardiac hypertrophy and a shortened lifespan. Moreover, the GAC signal is exponentially increased in pathological senescence induced by bleomycin in the lung. Senolytic dasatinib and quercetin (D + Q) reduce GAC signal in bleomycin treated mice. Thus, the Glb1-2A-mCherry reporter mice monitors systemic aging and function decline, predicts lifespan, and may facilitate the understanding of aging mechanisms and help in the development of Anti-aging interventions.

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