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Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin
Heterochronic blood sharing rejuvenates old tissues, and most of the studies on how this works focus on young plasma, its fractions, and a few youthful systemic candidates. However, it was not formally established that young blood is necessary for this multi-tissue rejuvenation. Here, using our rece...
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/PMC7288913/ https://www.ncbi.nlm.nih.gov/pubmed/32474458 http://dx.doi.org/10.18632/aging.103418 |
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author | Mehdipour, Melod Skinner, Colin Wong, Nathan Lieb, Michael Liu, Chao Etienne, Jessy Kato, Cameron Kiprov, Dobri Conboy, Michael J. Conboy, Irina M. |
author_facet | Mehdipour, Melod Skinner, Colin Wong, Nathan Lieb, Michael Liu, Chao Etienne, Jessy Kato, Cameron Kiprov, Dobri Conboy, Michael J. Conboy, Irina M. |
author_sort | Mehdipour, Melod |
collection | PubMed |
description | Heterochronic blood sharing rejuvenates old tissues, and most of the studies on how this works focus on young plasma, its fractions, and a few youthful systemic candidates. However, it was not formally established that young blood is necessary for this multi-tissue rejuvenation. Here, using our recently developed small animal blood exchange process, we replaced half of the plasma in mice with saline containing 5% albumin (terming it a “neutral” age blood exchange, NBE) thus diluting the plasma factors and replenishing the albumin that would be diminished if only saline was used. Our data demonstrate that a single NBE suffices to meet or exceed the rejuvenative effects of enhancing muscle repair, reducing liver adiposity and fibrosis, and increasing hippocampal neurogenesis in old mice, all the key outcomes seen after blood heterochronicity. Comparative proteomic analysis on serum from NBE, and from a similar human clinical procedure of therapeutic plasma exchange (TPE), revealed a molecular re-setting of the systemic signaling milieu, interestingly, elevating the levels of some proteins, which broadly coordinate tissue maintenance and repair and promote immune responses. Moreover, a single TPE yielded functional blood rejuvenation, abrogating the typical old serum inhibition of progenitor cell proliferation. Ectopically added albumin does not seem to be the sole determinant of such rejuvenation, and levels of albumin do not decrease with age nor are increased by NBE/TPE. A model of action (supported by a large body of published data) is that significant dilution of autoregulatory proteins that crosstalk to multiple signaling pathways (with their own feedback loops) would, through changes in gene expression, have long-lasting molecular and functional effects that are consistent with our observations. This work improves our understanding of the systemic paradigms of multi-tissue rejuvenation and suggest a novel and immediate use of the FDA approved TPE for improving the health and resilience of older people. |
format | Online Article Text |
id | pubmed-7288913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-72889132020-06-22 Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin Mehdipour, Melod Skinner, Colin Wong, Nathan Lieb, Michael Liu, Chao Etienne, Jessy Kato, Cameron Kiprov, Dobri Conboy, Michael J. Conboy, Irina M. Aging (Albany NY) Priority Research Paper Heterochronic blood sharing rejuvenates old tissues, and most of the studies on how this works focus on young plasma, its fractions, and a few youthful systemic candidates. However, it was not formally established that young blood is necessary for this multi-tissue rejuvenation. Here, using our recently developed small animal blood exchange process, we replaced half of the plasma in mice with saline containing 5% albumin (terming it a “neutral” age blood exchange, NBE) thus diluting the plasma factors and replenishing the albumin that would be diminished if only saline was used. Our data demonstrate that a single NBE suffices to meet or exceed the rejuvenative effects of enhancing muscle repair, reducing liver adiposity and fibrosis, and increasing hippocampal neurogenesis in old mice, all the key outcomes seen after blood heterochronicity. Comparative proteomic analysis on serum from NBE, and from a similar human clinical procedure of therapeutic plasma exchange (TPE), revealed a molecular re-setting of the systemic signaling milieu, interestingly, elevating the levels of some proteins, which broadly coordinate tissue maintenance and repair and promote immune responses. Moreover, a single TPE yielded functional blood rejuvenation, abrogating the typical old serum inhibition of progenitor cell proliferation. Ectopically added albumin does not seem to be the sole determinant of such rejuvenation, and levels of albumin do not decrease with age nor are increased by NBE/TPE. A model of action (supported by a large body of published data) is that significant dilution of autoregulatory proteins that crosstalk to multiple signaling pathways (with their own feedback loops) would, through changes in gene expression, have long-lasting molecular and functional effects that are consistent with our observations. This work improves our understanding of the systemic paradigms of multi-tissue rejuvenation and suggest a novel and immediate use of the FDA approved TPE for improving the health and resilience of older people. Impact Journals 2020-05-30 /pmc/articles/PMC7288913/ /pubmed/32474458 http://dx.doi.org/10.18632/aging.103418 Text en Copyright © 2020 Mehdipour et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Priority Research Paper Mehdipour, Melod Skinner, Colin Wong, Nathan Lieb, Michael Liu, Chao Etienne, Jessy Kato, Cameron Kiprov, Dobri Conboy, Michael J. Conboy, Irina M. Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin |
title | Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin |
title_full | Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin |
title_fullStr | Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin |
title_full_unstemmed | Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin |
title_short | Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin |
title_sort | rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin |
topic | Priority Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288913/ https://www.ncbi.nlm.nih.gov/pubmed/32474458 http://dx.doi.org/10.18632/aging.103418 |
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