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Mobilization‐based transplantation of young‐donor hematopoietic stem cells extends lifespan in mice

Mammalian aging is associated with reduced tissue regeneration and loss of physiological integrity. With age, stem cells diminish in their ability to regenerate adult tissues, likely contributing to age‐related morbidity. Thus, we replaced aged hematopoietic stem cells (HSCs) with young‐donor HSCs u...

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Autores principales: Guderyon, Michael J., Chen, Cang, Bhattacharjee, Anindita, Ge, Guo, Fernandez, Roman A., Gelfond, Jonathan A. L., Gorena, Karla M., Cheng, Catherine J., Li, Yang, Nelson, James F., Strong, Randy J., Hornsby, Peter J., Clark, Robert A., Li, Senlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7059148/
https://www.ncbi.nlm.nih.gov/pubmed/32012439
http://dx.doi.org/10.1111/acel.13110
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author Guderyon, Michael J.
Chen, Cang
Bhattacharjee, Anindita
Ge, Guo
Fernandez, Roman A.
Gelfond, Jonathan A. L.
Gorena, Karla M.
Cheng, Catherine J.
Li, Yang
Nelson, James F.
Strong, Randy J.
Hornsby, Peter J.
Clark, Robert A.
Li, Senlin
author_facet Guderyon, Michael J.
Chen, Cang
Bhattacharjee, Anindita
Ge, Guo
Fernandez, Roman A.
Gelfond, Jonathan A. L.
Gorena, Karla M.
Cheng, Catherine J.
Li, Yang
Nelson, James F.
Strong, Randy J.
Hornsby, Peter J.
Clark, Robert A.
Li, Senlin
author_sort Guderyon, Michael J.
collection PubMed
description Mammalian aging is associated with reduced tissue regeneration and loss of physiological integrity. With age, stem cells diminish in their ability to regenerate adult tissues, likely contributing to age‐related morbidity. Thus, we replaced aged hematopoietic stem cells (HSCs) with young‐donor HSCs using a novel mobilization‐enabled hematopoietic stem cell transplantation (HSCT) technology as an alternative to the highly toxic conditioning regimens used in conventional HSCT. Using this approach, we are the first to report an increase in median lifespan (12%) and a decrease in overall mortality hazard (HR: 0.42, CI: 0.273–0.638) in aged mice following transplantation of young‐donor HSCs. The increase in longevity was accompanied by reductions of frailty measures and increases in food intake and body weight of aged recipients. Young‐donor HSCs not only preserved youthful function within the aged bone marrow stroma, but also at least partially ameliorated dysfunctional hematopoietic phenotypes of aged recipients. This compelling evidence that mammalian health and lifespan can be extended through stem cell therapy adds a new category to the very limited list of successful anti‐aging/life‐extending interventions. Our findings have implications for further development of stem cell therapies for increasing health and lifespan.
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spelling pubmed-70591482020-03-11 Mobilization‐based transplantation of young‐donor hematopoietic stem cells extends lifespan in mice Guderyon, Michael J. Chen, Cang Bhattacharjee, Anindita Ge, Guo Fernandez, Roman A. Gelfond, Jonathan A. L. Gorena, Karla M. Cheng, Catherine J. Li, Yang Nelson, James F. Strong, Randy J. Hornsby, Peter J. Clark, Robert A. Li, Senlin Aging Cell Original Papers Mammalian aging is associated with reduced tissue regeneration and loss of physiological integrity. With age, stem cells diminish in their ability to regenerate adult tissues, likely contributing to age‐related morbidity. Thus, we replaced aged hematopoietic stem cells (HSCs) with young‐donor HSCs using a novel mobilization‐enabled hematopoietic stem cell transplantation (HSCT) technology as an alternative to the highly toxic conditioning regimens used in conventional HSCT. Using this approach, we are the first to report an increase in median lifespan (12%) and a decrease in overall mortality hazard (HR: 0.42, CI: 0.273–0.638) in aged mice following transplantation of young‐donor HSCs. The increase in longevity was accompanied by reductions of frailty measures and increases in food intake and body weight of aged recipients. Young‐donor HSCs not only preserved youthful function within the aged bone marrow stroma, but also at least partially ameliorated dysfunctional hematopoietic phenotypes of aged recipients. This compelling evidence that mammalian health and lifespan can be extended through stem cell therapy adds a new category to the very limited list of successful anti‐aging/life‐extending interventions. Our findings have implications for further development of stem cell therapies for increasing health and lifespan. John Wiley and Sons Inc. 2020-02-03 2020-03 /pmc/articles/PMC7059148/ /pubmed/32012439 http://dx.doi.org/10.1111/acel.13110 Text en © 2020 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Guderyon, Michael J.
Chen, Cang
Bhattacharjee, Anindita
Ge, Guo
Fernandez, Roman A.
Gelfond, Jonathan A. L.
Gorena, Karla M.
Cheng, Catherine J.
Li, Yang
Nelson, James F.
Strong, Randy J.
Hornsby, Peter J.
Clark, Robert A.
Li, Senlin
Mobilization‐based transplantation of young‐donor hematopoietic stem cells extends lifespan in mice
title Mobilization‐based transplantation of young‐donor hematopoietic stem cells extends lifespan in mice
title_full Mobilization‐based transplantation of young‐donor hematopoietic stem cells extends lifespan in mice
title_fullStr Mobilization‐based transplantation of young‐donor hematopoietic stem cells extends lifespan in mice
title_full_unstemmed Mobilization‐based transplantation of young‐donor hematopoietic stem cells extends lifespan in mice
title_short Mobilization‐based transplantation of young‐donor hematopoietic stem cells extends lifespan in mice
title_sort mobilization‐based transplantation of young‐donor hematopoietic stem cells extends lifespan in mice
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7059148/
https://www.ncbi.nlm.nih.gov/pubmed/32012439
http://dx.doi.org/10.1111/acel.13110
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