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Senescence-like phenotype in post-mitotic cells of mice entering middle age
Staining mice tissues for β-galactosidase activity is a fundamental tool to detect age- or disease-associated cellular senescence. However, reported analyses of positivity for senescence-associated β-galactosidase activity or for other markers of senescence in post-mitotic cells of healthy murine ti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425512/ https://www.ncbi.nlm.nih.gov/pubmed/32634782 http://dx.doi.org/10.18632/aging.103637 |
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author | Raffaele, Marco Kovacovicova, Kristina Bonomini, Francesca Rezzani, Rita Frohlich, Jan Vinciguerra, Manlio |
author_facet | Raffaele, Marco Kovacovicova, Kristina Bonomini, Francesca Rezzani, Rita Frohlich, Jan Vinciguerra, Manlio |
author_sort | Raffaele, Marco |
collection | PubMed |
description | Staining mice tissues for β-galactosidase activity is a fundamental tool to detect age- or disease-associated cellular senescence. However, reported analyses of positivity for senescence-associated β-galactosidase activity or for other markers of senescence in post-mitotic cells of healthy murine tissues have been fragmentary or inconclusive. Here, we attempted to independently deepen this knowledge using multiple senescence markers within the same cells of wild type mice entering middle age (9 months of age). A histochemistry protocol for the pH-dependent detection of β-galactosidase activity in several tissues was used. At pH 6, routinely utilized to detect senescence-associated β-galactosidase activity, only specific cellular populations in the mouse body (including Purkinje cells and choroid plexus in the central nervous system) were detected as strongly positive for β-galactosidase activity. These post-mitotic cells were also positive for other established markers of senescence (p16, p21 and DPP4), detected by immunofluorescence, confirming a potential senescent phenotype. These data might contribute to understanding the functional relation between the senescence-associated β-galactosidase activity and senescence markers in post-mitotic cells in absence of disease or advanced aging. |
format | Online Article Text |
id | pubmed-7425512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-74255122020-08-25 Senescence-like phenotype in post-mitotic cells of mice entering middle age Raffaele, Marco Kovacovicova, Kristina Bonomini, Francesca Rezzani, Rita Frohlich, Jan Vinciguerra, Manlio Aging (Albany NY) Research Paper Staining mice tissues for β-galactosidase activity is a fundamental tool to detect age- or disease-associated cellular senescence. However, reported analyses of positivity for senescence-associated β-galactosidase activity or for other markers of senescence in post-mitotic cells of healthy murine tissues have been fragmentary or inconclusive. Here, we attempted to independently deepen this knowledge using multiple senescence markers within the same cells of wild type mice entering middle age (9 months of age). A histochemistry protocol for the pH-dependent detection of β-galactosidase activity in several tissues was used. At pH 6, routinely utilized to detect senescence-associated β-galactosidase activity, only specific cellular populations in the mouse body (including Purkinje cells and choroid plexus in the central nervous system) were detected as strongly positive for β-galactosidase activity. These post-mitotic cells were also positive for other established markers of senescence (p16, p21 and DPP4), detected by immunofluorescence, confirming a potential senescent phenotype. These data might contribute to understanding the functional relation between the senescence-associated β-galactosidase activity and senescence markers in post-mitotic cells in absence of disease or advanced aging. Impact Journals 2020-07-31 /pmc/articles/PMC7425512/ /pubmed/32634782 http://dx.doi.org/10.18632/aging.103637 Text en Copyright © 2020 Raffaele et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Raffaele, Marco Kovacovicova, Kristina Bonomini, Francesca Rezzani, Rita Frohlich, Jan Vinciguerra, Manlio Senescence-like phenotype in post-mitotic cells of mice entering middle age |
title | Senescence-like phenotype in post-mitotic cells of mice entering middle age |
title_full | Senescence-like phenotype in post-mitotic cells of mice entering middle age |
title_fullStr | Senescence-like phenotype in post-mitotic cells of mice entering middle age |
title_full_unstemmed | Senescence-like phenotype in post-mitotic cells of mice entering middle age |
title_short | Senescence-like phenotype in post-mitotic cells of mice entering middle age |
title_sort | senescence-like phenotype in post-mitotic cells of mice entering middle age |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425512/ https://www.ncbi.nlm.nih.gov/pubmed/32634782 http://dx.doi.org/10.18632/aging.103637 |
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