NAD+ augmentation with nicotinamide riboside improves lymphoid potential of Atm-/- and old mice HSCs.
Le ZongMayuri Tanaka-YanoBongsoo ParkHagai YanaiFerda T TurhanDeborah L CroteauJane TianEvandro Fei FangVilhelm A BohrIsabel BeermanPublished in: NPJ aging and mechanisms of disease (2021)
NAD+ supplementation has significant benefits in compromised settings, acting largely through improved mitochondrial function and DNA repair. Elevating NAD+ to physiological levels has been shown to improve the function of some adult stem cells, with implications that these changes will lead to sustained improvement of the tissue or system. Here, we examined the effect of elevating NAD+ levels in models with reduced hematopoietic stem cell (HSC) potential, ATM-deficient and aged WT mice, and showed that supplementation of nicotinamide riboside (NR), a NAD+ precursor, improved lymphoid lineage potential during supplementation. In aged mice, this improved lymphoid potential was maintained in competitive transplants and was associated with transcriptional repression of myeloid gene signatures in stem and lineage-committed progenitor cells after NR treatment. However, the altered transcriptional priming of the stem cells toward lymphoid lineages was not sustained in the aged mice after NR removal. These data characterize significant alterations to the lineage potential of functionally compromised HSCs after short-term exposure to NR treatment.
Keyphrases
- dna repair
- stem cells
- dna damage
- high fat diet induced
- gene expression
- human health
- transcription factor
- risk assessment
- hematopoietic stem cell
- acute myeloid leukemia
- dna damage response
- type diabetes
- dendritic cells
- young adults
- oxidative stress
- machine learning
- skeletal muscle
- deep learning
- adipose tissue
- cell therapy
- soft tissue