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NAD(+) augmentation with nicotinamide riboside improves lymphoid potential of Atm(−/−) and old mice HSCs

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...

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Autores principales: Zong, Le, Tanaka-Yano, Mayuri, Park, Bongsoo, Yanai, Hagai, Turhan, Ferda T., Croteau, Deborah L., Tian, Jane, Fang, Evandro F., Bohr, Vilhelm A., Beerman, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455618/
https://www.ncbi.nlm.nih.gov/pubmed/34548492
http://dx.doi.org/10.1038/s41514-021-00078-3
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author Zong, Le
Tanaka-Yano, Mayuri
Park, Bongsoo
Yanai, Hagai
Turhan, Ferda T.
Croteau, Deborah L.
Tian, Jane
Fang, Evandro F.
Bohr, Vilhelm A.
Beerman, Isabel
author_facet Zong, Le
Tanaka-Yano, Mayuri
Park, Bongsoo
Yanai, Hagai
Turhan, Ferda T.
Croteau, Deborah L.
Tian, Jane
Fang, Evandro F.
Bohr, Vilhelm A.
Beerman, Isabel
author_sort Zong, Le
collection PubMed
description 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.
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spelling pubmed-84556182021-10-07 NAD(+) augmentation with nicotinamide riboside improves lymphoid potential of Atm(−/−) and old mice HSCs Zong, Le Tanaka-Yano, Mayuri Park, Bongsoo Yanai, Hagai Turhan, Ferda T. Croteau, Deborah L. Tian, Jane Fang, Evandro F. Bohr, Vilhelm A. Beerman, Isabel NPJ Aging Mech Dis Article 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. Nature Publishing Group UK 2021-09-21 /pmc/articles/PMC8455618/ /pubmed/34548492 http://dx.doi.org/10.1038/s41514-021-00078-3 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zong, 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
title NAD(+) augmentation with nicotinamide riboside improves lymphoid potential of Atm(−/−) and old mice HSCs
title_full NAD(+) augmentation with nicotinamide riboside improves lymphoid potential of Atm(−/−) and old mice HSCs
title_fullStr NAD(+) augmentation with nicotinamide riboside improves lymphoid potential of Atm(−/−) and old mice HSCs
title_full_unstemmed NAD(+) augmentation with nicotinamide riboside improves lymphoid potential of Atm(−/−) and old mice HSCs
title_short NAD(+) augmentation with nicotinamide riboside improves lymphoid potential of Atm(−/−) and old mice HSCs
title_sort nad(+) augmentation with nicotinamide riboside improves lymphoid potential of atm(−/−) and old mice hscs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455618/
https://www.ncbi.nlm.nih.gov/pubmed/34548492
http://dx.doi.org/10.1038/s41514-021-00078-3
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