Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-017-00935-4
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dc.titleThe telomere binding protein Pot1 maintains haematopoietic stem cell activity with age
dc.contributor.authorHosokawa, K
dc.contributor.authorMacArthur, B.D
dc.contributor.authorIkushima, Y.M
dc.contributor.authorToyama, H
dc.contributor.authorMasuhiro, Y
dc.contributor.authorHanazawa, S
dc.contributor.authorSuda, T
dc.contributor.authorArai, F
dc.date.accessioned2020-10-20T10:22:02Z
dc.date.available2020-10-20T10:22:02Z
dc.date.issued2017
dc.identifier.citationHosokawa, K, MacArthur, B.D, Ikushima, Y.M, Toyama, H, Masuhiro, Y, Hanazawa, S, Suda, T, Arai, F (2017). The telomere binding protein Pot1 maintains haematopoietic stem cell activity with age. Nature Communications 8 (1) : 804. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-017-00935-4
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178570
dc.description.abstractRepeated cell divisions and aging impair stem cell function. However, the mechanisms by which this occurs are not fully understood. Here we show that protection of telomeres 1A (Pot1a), a component of the Shelterin complex that protects telomeres, improves haematopoietic stem cell (HSC) activity during aging. Pot1a is highly expressed in young HSCs, but declines with age. In mouse HSCs, Pot1a knockdown increases DNA damage response (DDR) and inhibits self-renewal. Conversely, Pot1a overexpression or treatment with POT1a protein prevents DDR, maintained self-renewal activity and rejuvenated aged HSCs upon ex vivo culture. Moreover, treatment of HSCs with exogenous Pot1a inhibits the production of reactive oxygen species, suggesting a non-Telomeric role for Pot1a in HSC maintenance. Consistent with these results, treatment with exogenous human POT1 protein maintains human HSC activity in culture. Collectively, these results show that Pot1a/POT1 sustains HSC activity and can be used to expand HSC numbers ex vivo. © 2017 The Author(s).
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectPot1 protein
dc.subjectreactive oxygen metabolite
dc.subjecttelomere binding protein
dc.subjectunclassified drug
dc.subjectDNA binding protein
dc.subjectPOT1 protein, mouse
dc.subjectreactive oxygen metabolite
dc.subjectage
dc.subjectcells and cell components
dc.subjectchromosome
dc.subjectDNA
dc.subjectgene expression
dc.subjectprotein
dc.subjectreactive oxygen species
dc.subjectanimal cell
dc.subjectapoptosis
dc.subjectArticle
dc.subjectcell activity
dc.subjectcell aging
dc.subjectcell differentiation
dc.subjectcell function
dc.subjectcell protection
dc.subjectcell survival
dc.subjectcontrolled study
dc.subjectDNA damage response
dc.subjectdown regulation
dc.subjectex vivo study
dc.subjectgene expression
dc.subjecthematopoietic stem cell
dc.subjecthuman
dc.subjecthuman cell
dc.subjectmicroarray analysis
dc.subjectmouse
dc.subjectnonhuman
dc.subjectoxidative phosphorylation
dc.subjectprotein expression
dc.subjectprotein function
dc.subjectrejuvenation
dc.subjectsenescence
dc.subjectstem cell culture
dc.subjectstem cell expansion
dc.subjectstem cell self-renewal
dc.subjectanimal
dc.subjectcell aging
dc.subjectcell culture
dc.subjectDNA damage
dc.subjectgenetics
dc.subjecthematopoietic stem cell
dc.subjectmetabolism
dc.subjectphysiology
dc.subjecttelomere
dc.subjectAnimals
dc.subjectCells, Cultured
dc.subjectCellular Senescence
dc.subjectDNA Damage
dc.subjectDNA-Binding Proteins
dc.subjectHematopoietic Stem Cells
dc.subjectHumans
dc.subjectMice
dc.subjectReactive Oxygen Species
dc.subjectTelomere
dc.typeArticle
dc.contributor.departmentDEPT OF MEDICINE
dc.description.doi10.1038/s41467-017-00935-4
dc.description.sourcetitleNature Communications
dc.description.volume8
dc.description.issue1
dc.description.page804
dc.published.statepublished
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