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

  • David Frescas
  • , Brandon M. Hall
  • , Evguenia Strom
  • , Lauren P. Virtuoso
  • , Mahima Gupta
  • , Anatoli S. Gleiberman
  • , Elena Rydkina
  • , Vitaly Balan
  • , Slavoljub Vujcic
  • , Olga B. Chernova
  • , Andrei V. Gudkov
  • Everon Biosciences, Inc.

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

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.

Original languageEnglish
Pages (from-to)1526-1533
Number of pages8
JournalCell Cycle
Volume16
Issue number16
DOIs
StatePublished - Aug 18 2017

Keywords

  • biomarkers
  • healthspan
  • p16(Ink4a)
  • senescence
  • senescence-associated β-galactosidase (SA-βGal)

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