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 language | English |
|---|---|
| Pages (from-to) | 1526-1533 |
| Number of pages | 8 |
| Journal | Cell Cycle |
| Volume | 16 |
| Issue number | 16 |
| DOIs | |
| State | Published - Aug 18 2017 |
Keywords
- biomarkers
- healthspan
- p16(Ink4a)
- senescence
- senescence-associated β-galactosidase (SA-βGal)
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