NAD+ supplementation prevents STING-induced senescence in CD8+ T cells by improving mitochondrial homeostasis

J Cell Biochem. 2024 Mar;125(3):e30522. doi: 10.1002/jcb.30522. Epub 2024 Jan 15.

Abstract

Understanding the connection between senescence phenotypes and mitochondrial dysfunction is crucial in aging and premature aging diseases. Loss of mitochondrial function leads to a decline in T cell function, which plays a significant role in this process. However, more research is required to determine if improving mitochondrial homeostasis alleviates senescence phenotypes. Our research has shown an association between NAD+ and senescent T cells through the cGAS-STING pathway, which can lead to an inflammatory phenotype. Further research is needed to fully understand the role of NAD+ in T-cell aging and how it can be utilized to improve mitochondrial homeostasis and alleviate senescence phenotypes. We demonstrate here that mitochondrial dysfunction and cellular senescence with a senescence-associated secretory phenotype (SASP) occur in senescent T cells and tumor-bearing mice. Senescence is mediated by a stimulator of interferon genes (STING) and involves ectopic cytoplasmic DNA. We further show that boosting intracellular NAD+ levels with nicotinamide mononucleotide (NMN) prevents senescence and SASP by promoting mitophagy. NMN treatment also suppresses senescence and neuroinflammation and improves the survival cycle of mice. Encouraging mitophagy may be a useful strategy to prevent CD8+ T cells from senescence due to mitochondrial dysfunction. Additionally, supplementing with NMN to increase NAD+ levels could enhance survival rates in mice while also reducing senescence and inflammation, and enhancing mitophagy as a potential therapeutic intervention.

Keywords: SASP; cGAS-STING; mitochondria; nicotinamide mononucleotide; senescence.

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / metabolism
  • Cellular Senescence / physiology
  • Dietary Supplements
  • Homeostasis
  • Mice
  • Mitochondria / metabolism
  • Mitochondrial Diseases* / metabolism
  • NAD* / metabolism

Substances

  • NAD