Publication:
Long Live Partial Reprogramming.

dc.contributor.authorMarión, Rosa M
dc.contributor.authorBlasco, MA
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderFundacion Botines_ES
dc.date.accessioned2024-04-03T11:36:37Z
dc.date.available2024-04-03T11:36:37Z
dc.date.issued2017-04-28
dc.description.abstractAging can be defined as the progressive loss of physiological integrity that leads to tissue dysfunction and increased risk for developing age-associated human pathologies, such as cancer, diabetes mellitus, cardiovascular disorders, and neurodegenerative diseases.(1) Therapeutic strategies to delay or prevent aging are aimed to decrease the deleterious effects of aging and to improve the quality of life in aged individuals and eventually to extend the human life span. In addition, deep molecular understanding of the mechanisms of aging may lead to new treatments for age-related diseases. In line with this, a recent article in Cell(2) shows that cyclic induction of Yamanaka reprogramming factors in vitro, what the authors called "partial reprogramming," reduces age-associated features in mouse and human cells. Strikingly, partial reprogramming induced in vivo in a mouse model of premature aging ameliorates some aging-associated hallmarks and extends their prematurely shortened life span. Importantly, these beneficial effects are not accompanied by dedifferentiation or loss of cellular identity. Finally, the authors show that partial in vivo reprogramming increases the regenerative capacity of physiologically aged wild-type mice.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipWork in the laboratory of M.A.B. is funded by the Spanish Ministry of Economy and Competiveness (PLAN RETOS) and by the Fundacion Botin.es_ES
dc.format.number9es_ES
dc.format.page1381es_ES
dc.format.volume120es_ES
dc.identifier.citationCirc Res . 2017 Apr ;120(9):1381-1383.es_ES
dc.identifier.doi10.1161/CIRCRESAHA.117.310594es_ES
dc.identifier.e-issn1524-4571es_ES
dc.identifier.journalCirculation researches_ES
dc.identifier.pubmedID28450358es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/19110
dc.language.isoenges_ES
dc.publisherLippincott Williams & Wilkins (LWW)
dc.relation.publisherversionhttps://doi.org/10.1161/CIRCRESAHA.117.310594.es_ES
dc.repisalud.institucionCNIOes_ES
dc.repisalud.orgCNIOCNIO::Grupos de investigación::Grupo de Telómeros y Telomerasaes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshCellular Reprogramminges_ES
dc.subject.meshInduced Pluripotent Stem Cellses_ES
dc.titleLong Live Partial Reprogramming.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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