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Do senescence markers correlate in vitro and in situ within individual human donors?
Waaijer, Mariëtte E C; Gunn, David A; van Heemst, Diana; Slagboom, P Eline; Sedivy, John M; Dirks, Roeland W; Tanke, Hans J; Westendorp, Rudi G J; Maier, Andrea B.
Affiliation
  • Waaijer MEC; Department of Gerontology and Geriatrics, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.
  • Gunn DA; Unilever Discover, Colworth Science Park, Sharnbrook, Bedfordshire MK44 1LQ, UK.
  • van Heemst D; Department of Gerontology and Geriatrics, Leiden University Medical Center, 2300 RC Leiden, the Netherlands.
  • Slagboom PE; Netherlands Consortium for Healthy Aging, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
  • Sedivy JM; Netherlands Consortium for Healthy Aging, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
  • Dirks RW; Department of Molecular Epidemiology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
  • Tanke HJ; Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI 02912, USA.
  • Westendorp RGJ; Department of Molecular Cell Biology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
  • Maier AB; Department of Molecular Cell Biology, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.
Aging (Albany NY) ; 10(2): 278-289, 2018 02 28.
Article in En | MEDLINE | ID: mdl-29500330
ABSTRACT
Little is known on how well senescence markers in vitro and in situ correlate within individual donors. We studied correlations between the same and different in vitro markers. Furthermore, we tested correlations between in vitro markers with in situ p16INK4a positivity.From 100 donors (20-91 years), cultured dermal fibroblasts were assessed for reactive oxygen species (ROS), telomere-associated foci (TAF), p16INK4a and senescence-associated ß-gal (SAß-gal), with/ without 0.6 µM rotenone for 3 days (short-term). In fibroblasts from 40 donors, telomere shortening, ROS and SAß-gal were additionally assessed, with/ without 20 nM rotenone for 7 weeks (long-term). In skin from 52 donors, the number of p16INK4a positive dermal cells was assessed in situ.More than half of the correlations of the same senescence markers in vitro between duplicate experiments and between short-term versus long-term experiments were significant. Half of the different senescence marker correlations were significant within the short-term and within the long-term experiments. The different senescence markers in vitro were not significantly correlated intra-individually with in situ p16INK4a positivity.In conclusion, the same and different senescence markers are frequently correlated significantly within and between in vitro experiments, but in vitro senescence markers are not correlated with p16INK4a positivity in situ.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Telomere / Cellular Senescence / Beta-Galactosidase / Genes, p16 Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Aging (Albany NY) Journal subject: GERIATRIA Year: 2018 Type: Article Affiliation country: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Telomere / Cellular Senescence / Beta-Galactosidase / Genes, p16 Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Aging (Albany NY) Journal subject: GERIATRIA Year: 2018 Type: Article Affiliation country: Netherlands