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Metabolic Alterations in Cellular Senescence: The Role of Citrate in Ageing and Age-Related Disease

期刊

出版社

MDPI
DOI: 10.3390/ijms23073652

关键词

senescence; telomere; metabolism; citrate; ageing; cancer; transport; energy

资金

  1. Queen Mary University of London Innovation Award
  2. Dunhill Medical Trust [R452/1115]
  3. DFG (Deutsche Forschungsgemeinschaft) [GE1188/5-1]

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Recent experiments in mouse models have shown that senescent cells play a crucial role in age-related diseases and may contribute to certain pathological conditions. The recognition of extranuclear chromatin by the cyclic GMP-AMP synthase-stimulator of interferon genes pathway leads to the induction of inflammatory cytokines, which are part of the senescence-associated secretory phenotype. This chronic inflammation increases with age and age-related diseases. In addition, senescent cells undergo metabolic changes, including the accumulation of extracellular citrate, which may also contribute to age-related diseases.
Recent mouse model experiments support an instrumental role for senescent cells in age-related diseases and senescent cells may be causal to certain age-related pathologies. A strongly supported hypothesis is that extranuclear chromatin is recognized by the cyclic GMP-AMP synthase-stimulator of interferon genes pathway, which in turn leads to the induction of several inflammatory cytokines as part of the senescence-associated secretory phenotype. This sterile inflammation increases with chronological age and age-associated disease. More recently, several intracellular and extracellular metabolic changes have been described in senescent cells but it is not clear whether any of them have functional significance. In this review, we highlight the potential effect of dietary and age-related metabolites in the modulation of the senescent phenotype in addition to discussing how experimental conditions may influence senescent cell metabolism, especially that of energy regulation. Finally, as extracellular citrate accumulates following certain types of senescence, we focus on the recently reported role of extracellular citrate in aging and age-related pathologies. We propose that citrate may be an active component of the senescence-associated secretory phenotype and via its intake through the diet may even contribute to the cause of age-related disease.

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