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dc.date.accessioned2022-02-28T18:17:59Z
dc.date.available2022-02-28T18:17:59Z
dc.date.created2021-10-05T14:49:39Z
dc.date.issued2021
dc.identifier.citationZong, Le Tanaka-Yano, Mayuri Park, Bongsoo Yanai, Hagai Turhan, Ferda T. Croteau, Deborah L. Tian, Jane Fang, Evandro F. Bohr, Vilhelm A. Beerman, Isabel . NAD+ augmentation with nicotinamide riboside improves lymphoid potential of Atm−/− and old mice HSCs. npj Aging and Mechanisms of Disease. 2021, 7(1), 1-9
dc.identifier.urihttp://hdl.handle.net/10852/91614
dc.description.abstractNAD+ 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.
dc.languageEN
dc.publisherNature Portfolio
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleNAD+ augmentation with nicotinamide riboside improves lymphoid potential of Atm−/− and old mice HSCs
dc.typeJournal article
dc.creator.authorZong, Le
dc.creator.authorTanaka-Yano, Mayuri
dc.creator.authorPark, Bongsoo
dc.creator.authorYanai, Hagai
dc.creator.authorTurhan, Ferda T.
dc.creator.authorCroteau, Deborah L.
dc.creator.authorTian, Jane
dc.creator.authorFang, Evandro F.
dc.creator.authorBohr, Vilhelm A.
dc.creator.authorBeerman, Isabel
cristin.unitcode185,53,82,10
cristin.unitnameAvdeling for klinisk molekylærbiologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1943474
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=npj Aging and Mechanisms of Disease&rft.volume=7&rft.spage=1&rft.date=2021
dc.identifier.jtitlenpj Aging and Mechanisms of Disease
dc.identifier.volume7
dc.identifier.issue1
dc.identifier.startpage1
dc.identifier.endpage9
dc.identifier.doihttps://doi.org/10.1038/s41514-021-00078-3
dc.identifier.urnURN:NBN:no-94188
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2731-6068
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/91614/1/s41514-021-00078-3.pdf
dc.type.versionPublishedVersion
cristin.articleid25


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