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dc.contributor.authorIgarashi, Masaki
dc.contributor.authorMiura, Masaomi
dc.contributor.authorWilliams, Eric O
dc.contributor.authorJaksch, Frank
dc.contributor.authorKadowaki, Takashi
dc.contributor.authorYamauchi, Toshimasa
dc.contributor.authorGuarente, Leonard Pershing
dc.date.accessioned2020-05-22T12:32:56Z
dc.date.available2020-05-22T12:32:56Z
dc.date.issued2019-03
dc.date.submitted2019-01
dc.identifier.issn1474-9718
dc.identifier.issn1474-9726
dc.identifier.urihttps://hdl.handle.net/1721.1/125404
dc.description.abstractThe tissue decline due to aging is associated with the deterioration of adult stem cell function. Here we show the number and proliferative activity of intestinal stem cells (ISCs) but not Paneth cells decline during aging, as does ISC function assessed ex vivo. Levels of SIRT1 and activity of mTORC1 also decline with aging. The treatment with the NAD(+) precursor nicotinamide riboside (NR) rejuvenates ISCs from aged mice and reverses an impaired ability to repair gut damage. The effect of NR is blocked by the mTORC1 inhibitor rapamycin or the SIRT1 inhibitor EX527. These findings demonstrate that small molecules affecting the NAD/SIRT1/mTORC1 axis may guide a translational path for maintenance of the intestine during aging. Keywords: aging; intestinal stem cells; NAD+; nicotinamide ribosideen_US
dc.language.isoen
dc.publisherWileyen_US
dc.relation.isversionofhttps://dx.doi.org/10.1111/acel.12935en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceWileyen_US
dc.titleNAD + supplementation rejuvenates aged gut adult stem cellsen_US
dc.typeArticleen_US
dc.identifier.citationIgarashi, Masaki et al. "NAD + supplementation rejuvenates aged gut adult stem cells." Aging Cell 18,3 (June 2019): e12935 © 2019 The Author(s).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentPaul F. Glenn Center for Biology of Aging Research (Massachusetts Institute of Technology)en_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.relation.journalAging Cellen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-12-05T16:45:18Z
dspace.date.submission2019-12-05T16:45:20Z
mit.journal.volume18en_US
mit.journal.issue3en_US
mit.metadata.statusComplete


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