Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/171498
Title: In Vivo Reprogramming Ameliorates Aging Features in Dentate Gyrus Cells and Improves Memory in Mice
Author: Rodríguez Matellán, Alberto
Alcazar, Noelia
Hernández, Félix
Serrano Marugán, Manuel
Ávila, Jesús
Keywords: Epigenètica
Malalties neurodegeneratives
Ratolins (Animals de laboratori)
Epigenetics
Neurodegenerative diseases
Mice (Laboratory animals)
Issue Date: 22-Oct-2020
Abstract: Post-translational epigenetic modifications take place in mouse neurons of the dentate gyrus (DG) with age. Here, we report that age-dependent reduction in H3K9 trimethylation (H3K9me3) is prevented by cyclic induction of the Yamanaka factors used for cell reprogramming. Interestingly, Yamanaka factors elevated the levels of migrating cells containing the neurogenic markers doublecortin and calretinin, and the levels of the NMDA receptor subunit GluN2B. These changes could result in an increase in the survival of newborn DG neurons during their maturation and higher synaptic plasticity in mature neurons. Importantly, these cellular changes were accompanied by an improvement in mouse performance in the object recognition test over long time. We conclude that transient cyclic reprogramming in vivo in the central nervous system could be an effective strategy to ameliorate aging of the central nervous system and neurodegenerative diseases.
Note: Reproducció del document publicat a: https://doi.org/10.1016/j.stemcr.2020.09.010
It is part of: Stem Cell Reports, 2020
URI: http://hdl.handle.net/2445/171498
Related resource: https://doi.org/10.1016/j.stemcr.2020.09.010
DOI: 10.1016/j.stemcr.2020.09.010
Appears in Collections:Articles publicats en revistes (Institut de Recerca Biomèdica (IRB Barcelona))



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