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Anti-aging mechanism of different age donor-matched adipose-derived stem cells
BACKGROUND: Adipose-derived stem cells (ASCs) have anti-aging and anti-obesity effects in aged animals, but the underlying molecular mechanism remains unknown. METHODS: In the present study, we evaluated the in vivo transplantation effects of different age donor-matched ASCs on natural aging and lep...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394785/ https://www.ncbi.nlm.nih.gov/pubmed/37533129 http://dx.doi.org/10.1186/s13287-023-03415-3 |
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author | Wang, Tao Li, Yingyu Zhu, Yu Liu, Zebiao Huang, Li Zhao, Hongxia Zhou, Zuping Wu, Qiong |
author_facet | Wang, Tao Li, Yingyu Zhu, Yu Liu, Zebiao Huang, Li Zhao, Hongxia Zhou, Zuping Wu, Qiong |
author_sort | Wang, Tao |
collection | PubMed |
description | BACKGROUND: Adipose-derived stem cells (ASCs) have anti-aging and anti-obesity effects in aged animals, but the underlying molecular mechanism remains unknown. METHODS: In the present study, we evaluated the in vivo transplantation effects of different age donor-matched ASCs on natural aging and leptin knockout mice (ob(−)/ob(−) mice). The multi-omics expression profiles of young and aged mouse donor-derived ASCs were also analyzed. RESULTS: The results revealed that ASCs from young donors induced weight and abdominal fat loss for older recipients but not for young or ob(−)/ob(−)mice. The young and aged mouse donor ASCs displayed significant phenotypic differences, contributing to the distinguished weight loss and anti-aging effects in aged mice. CONCLUSIONS: Our data suggest an underlying molecular mechanism by which young-donor ASCs reduce immune cells and inflammation in aged mice via secreted immune factors. These findings point to a general anti-aging mechanism of stem cells, which may provide new insights into age-related disturbances of stem cell plasticity in healthy aging and age-related diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03415-3. |
format | Online Article Text |
id | pubmed-10394785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103947852023-08-03 Anti-aging mechanism of different age donor-matched adipose-derived stem cells Wang, Tao Li, Yingyu Zhu, Yu Liu, Zebiao Huang, Li Zhao, Hongxia Zhou, Zuping Wu, Qiong Stem Cell Res Ther Research BACKGROUND: Adipose-derived stem cells (ASCs) have anti-aging and anti-obesity effects in aged animals, but the underlying molecular mechanism remains unknown. METHODS: In the present study, we evaluated the in vivo transplantation effects of different age donor-matched ASCs on natural aging and leptin knockout mice (ob(−)/ob(−) mice). The multi-omics expression profiles of young and aged mouse donor-derived ASCs were also analyzed. RESULTS: The results revealed that ASCs from young donors induced weight and abdominal fat loss for older recipients but not for young or ob(−)/ob(−)mice. The young and aged mouse donor ASCs displayed significant phenotypic differences, contributing to the distinguished weight loss and anti-aging effects in aged mice. CONCLUSIONS: Our data suggest an underlying molecular mechanism by which young-donor ASCs reduce immune cells and inflammation in aged mice via secreted immune factors. These findings point to a general anti-aging mechanism of stem cells, which may provide new insights into age-related disturbances of stem cell plasticity in healthy aging and age-related diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03415-3. BioMed Central 2023-08-02 /pmc/articles/PMC10394785/ /pubmed/37533129 http://dx.doi.org/10.1186/s13287-023-03415-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wang, Tao Li, Yingyu Zhu, Yu Liu, Zebiao Huang, Li Zhao, Hongxia Zhou, Zuping Wu, Qiong Anti-aging mechanism of different age donor-matched adipose-derived stem cells |
title | Anti-aging mechanism of different age donor-matched adipose-derived stem cells |
title_full | Anti-aging mechanism of different age donor-matched adipose-derived stem cells |
title_fullStr | Anti-aging mechanism of different age donor-matched adipose-derived stem cells |
title_full_unstemmed | Anti-aging mechanism of different age donor-matched adipose-derived stem cells |
title_short | Anti-aging mechanism of different age donor-matched adipose-derived stem cells |
title_sort | anti-aging mechanism of different age donor-matched adipose-derived stem cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394785/ https://www.ncbi.nlm.nih.gov/pubmed/37533129 http://dx.doi.org/10.1186/s13287-023-03415-3 |
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