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Heterochronic parabiosis: a valuable tool to investigate cellular senescence and other hallmarks of aging
Parabiosis is a well-established method to facilitate a shared blood supply between two conjoined animals. In particular, the pairing of mice of dissimilar ages, termed heterochronic parabiosis, has been used extensively for differentiating cell autonomous and non-autonomous mechanisms of aging. Ana...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037264/ https://www.ncbi.nlm.nih.gov/pubmed/35417855 http://dx.doi.org/10.18632/aging.204015 |
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author | Yousefzadeh, Matthew J. Robbins, Paul D. Huffman, Derek M. |
author_facet | Yousefzadeh, Matthew J. Robbins, Paul D. Huffman, Derek M. |
author_sort | Yousefzadeh, Matthew J. |
collection | PubMed |
description | Parabiosis is a well-established method to facilitate a shared blood supply between two conjoined animals. In particular, the pairing of mice of dissimilar ages, termed heterochronic parabiosis, has been used extensively for differentiating cell autonomous and non-autonomous mechanisms of aging. Analysis of heterochronic parabionts also has helped to identify individual circulating factors that may act as either pro- or anti-geronics. Heterochronic parabiosis also has proven to be a valuable experimental system to evaluate the effects of specific hallmarks of aging on the process of aging. For example, heterochronic parabiosis was used recently to examine whether cellular senescence was driven via cell autonomous and/or non-autonomous mechanisms. As anticipated, markers of cellular senescence were elevated in old isochronically-paired mice relative to young controls. However, compared to old isochronically paired mice, the senescent cell burden was reduced in multiple tissues of old parabionts joined with young mice. This suggests that the rejuvenation of cells and tissues in old mice by exposure to young blood could be mediated, in part, through suppression or immune clearance of senescent cells. Conversely, young heterochronic parabionts showed increased markers of cellular senescence, demonstrating that exposure to an old circulation is able to drive senescence through a cell non-autonomous mechanism(s), likely contributing to accelerated aging in the young mice. Thus, heterochronic parabiosis is still an important methodology that should continue to be leveraged for evaluating other hallmarks of aging and their mechanisms. |
format | Online Article Text |
id | pubmed-9037264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-90372642022-04-26 Heterochronic parabiosis: a valuable tool to investigate cellular senescence and other hallmarks of aging Yousefzadeh, Matthew J. Robbins, Paul D. Huffman, Derek M. Aging (Albany NY) Research Perspective Parabiosis is a well-established method to facilitate a shared blood supply between two conjoined animals. In particular, the pairing of mice of dissimilar ages, termed heterochronic parabiosis, has been used extensively for differentiating cell autonomous and non-autonomous mechanisms of aging. Analysis of heterochronic parabionts also has helped to identify individual circulating factors that may act as either pro- or anti-geronics. Heterochronic parabiosis also has proven to be a valuable experimental system to evaluate the effects of specific hallmarks of aging on the process of aging. For example, heterochronic parabiosis was used recently to examine whether cellular senescence was driven via cell autonomous and/or non-autonomous mechanisms. As anticipated, markers of cellular senescence were elevated in old isochronically-paired mice relative to young controls. However, compared to old isochronically paired mice, the senescent cell burden was reduced in multiple tissues of old parabionts joined with young mice. This suggests that the rejuvenation of cells and tissues in old mice by exposure to young blood could be mediated, in part, through suppression or immune clearance of senescent cells. Conversely, young heterochronic parabionts showed increased markers of cellular senescence, demonstrating that exposure to an old circulation is able to drive senescence through a cell non-autonomous mechanism(s), likely contributing to accelerated aging in the young mice. Thus, heterochronic parabiosis is still an important methodology that should continue to be leveraged for evaluating other hallmarks of aging and their mechanisms. Impact Journals 2022-04-13 /pmc/articles/PMC9037264/ /pubmed/35417855 http://dx.doi.org/10.18632/aging.204015 Text en Copyright: © 2022 Yousefzadeh et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Perspective Yousefzadeh, Matthew J. Robbins, Paul D. Huffman, Derek M. Heterochronic parabiosis: a valuable tool to investigate cellular senescence and other hallmarks of aging |
title | Heterochronic parabiosis: a valuable tool to investigate cellular senescence and other hallmarks of aging |
title_full | Heterochronic parabiosis: a valuable tool to investigate cellular senescence and other hallmarks of aging |
title_fullStr | Heterochronic parabiosis: a valuable tool to investigate cellular senescence and other hallmarks of aging |
title_full_unstemmed | Heterochronic parabiosis: a valuable tool to investigate cellular senescence and other hallmarks of aging |
title_short | Heterochronic parabiosis: a valuable tool to investigate cellular senescence and other hallmarks of aging |
title_sort | heterochronic parabiosis: a valuable tool to investigate cellular senescence and other hallmarks of aging |
topic | Research Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037264/ https://www.ncbi.nlm.nih.gov/pubmed/35417855 http://dx.doi.org/10.18632/aging.204015 |
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