Literature DB >> 28650766

Murine mesenchymal cells that express elevated levels of the CDK inhibitor p16(Ink4a) in vivo are not necessarily senescent.

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)

Mesh:

Substances:

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


  21 in total

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Journal:  Nature       Date:  2016-02-03       Impact factor: 49.962

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Review 9.  Senolytic drugs: from discovery to translation.

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10.  Paradoxes of senolytics.

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