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Lookup NU author(s): Dr Ed FielderORCiD, Professor Thomas von Zglinicki
© 2021 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd.Cellular senescence is characterized by an irreversible cell cycle arrest and a pro-inflammatory senescence-associated secretory phenotype (SASP), which is a major contributor to aging and age-related diseases. Clearance of senescent cells has been shown to improve brain function in mouse models of neurodegenerative diseases. However, it is still unknown whether senescent cell clearance alleviates cognitive dysfunction during the aging process. To investigate this, we first conducted single-nuclei and single-cell RNA-seq in the hippocampus from young and aged mice. We observed an age-dependent increase in p16Ink4a senescent cells, which was more pronounced in microglia and oligodendrocyte progenitor cells and characterized by a SASP. We then aged INK-ATTAC mice, in which p16Ink4a-positive senescent cells can be genetically eliminated upon treatment with the drug AP20187 and treated them either with AP20187 or with the senolytic cocktail Dasatinib and Quercetin. We observed that both strategies resulted in a decrease in p16Ink4a exclusively in the microglial population, resulting in reduced microglial activation and reduced expression of SASP factors. Importantly, both approaches significantly improved cognitive function in aged mice. Our data provide proof-of-concept for senolytic interventions' being a potential therapeutic avenue for alleviating age-associated cognitive impairment.
Author(s): Ogrodnik M, Evans SA, Fielder E, Victorelli S, Kruger P, Salmonowicz H, Weigand BM, Patel AD, Pirtskhalava T, Inman CL, Johnson KO, Dickinson SL, Rocha A, Schafer MJ, Zhu Y, Allison DB, von Zglinicki T, LeBrasseur NK, Tchkonia T, Neretti N, Passos JF, Kirkland JL, Jurk D
Publication type: Article
Publication status: Published
Journal: Aging Cell
Year: 2021
Volume: 20
Issue: 2
Print publication date: 01/02/2021
Online publication date: 20/01/2021
Acceptance date: 06/12/2020
Date deposited: 19/10/2023
ISSN (print): 1474-9718
ISSN (electronic): 1474-9726
Publisher: Blackwell Publishing Ltd
URL: https://doi.org/10.1111/acel.13296
DOI: 10.1111/acel.13296
Data Access Statement: The datasets generated during and/or analyzed during the current study will available in the NCBI GEO repository after publication and the accession codes is GSE161340 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE161340). All data generated or analyzed during this study are available from the corresponding author on reasonable request.
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