| Literature DB >> 28650766 |
David Frescas1, Brandon M Hall1, Evguenia Strom1, Lauren P Virtuoso1, Mahima Gupta1, Anatoli S Gleiberman1, Elena Rydkina1, Vitaly Balan1, Slavoljub Vujcic1, Olga B Chernova1, Andrei V Gudkov1,2.
Abstract
Age-related health decline has been attributed to the accumulation of senescent cells recognized in vivo by p16(Ink4a) expression. The pharmacological elimination of p16(Ink4a)-positive cells from the tissues of mice was shown to extend a healthy lifespan. Here, we describe a population of mesenchymal cells isolated from mice that are highly p16(INK4a)-positive are proficient in proliferation but lack other properties of cellular senescence. These data, along with earlier reports on p16(Ink4a)-positive macrophages, indicate that p16(Ink4a)-positive and senescent cell populations only partially intersect, therefore, extending the list of potential cellular targets for anti- aging therapies.Entities:
Keywords: biomarkers; healthspan; p16(Ink4a); senescence; senescence-associated β-galactosidase (SA-βGal)
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Year: 2017 PMID: 28650766 PMCID: PMC5584871 DOI: 10.1080/15384101.2017.1339850
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534