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Systemic GDF11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice
Aging is a negative regulator of general homeostasis, tissue function, and regeneration. Changes in organismal energy levels and physiology, through systemic manipulations such as calorie restriction and young blood infusion, can regenerate tissue activity and increase lifespan in aged mice. However...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974718/ https://www.ncbi.nlm.nih.gov/pubmed/31637864 http://dx.doi.org/10.1111/acel.13038 |
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author | Katsimpardi, Lida Kuperwasser, Nicolas Camus, Claire Moigneu, Carine Chiche, Aurélie Tolle, Virginie Li, Han Kokovay, Erzsebet Lledo, Pierre‐Marie |
author_facet | Katsimpardi, Lida Kuperwasser, Nicolas Camus, Claire Moigneu, Carine Chiche, Aurélie Tolle, Virginie Li, Han Kokovay, Erzsebet Lledo, Pierre‐Marie |
author_sort | Katsimpardi, Lida |
collection | PubMed |
description | Aging is a negative regulator of general homeostasis, tissue function, and regeneration. Changes in organismal energy levels and physiology, through systemic manipulations such as calorie restriction and young blood infusion, can regenerate tissue activity and increase lifespan in aged mice. However, whether these two systemic manipulations could be linked has never been investigated. Here, we report that systemic GDF11 triggers a calorie restriction‐like phenotype without affecting appetite or GDF15 levels in the blood, restores the insulin/IGF‐1 signaling pathway, and stimulates adiponectin secretion from white adipose tissue by direct action on adipocytes, while repairing neurogenesis in the aged brain. These findings suggest that GDF11 has a pleiotropic effect on an organismal level and that it could be a linking mechanism of rejuvenation between heterochronic parabiosis and calorie restriction. As such, GDF11 could be considered as an important therapeutic candidate for age‐related neurodegenerative and metabolic disorders. |
format | Online Article Text |
id | pubmed-6974718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69747182020-01-28 Systemic GDF11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice Katsimpardi, Lida Kuperwasser, Nicolas Camus, Claire Moigneu, Carine Chiche, Aurélie Tolle, Virginie Li, Han Kokovay, Erzsebet Lledo, Pierre‐Marie Aging Cell Original Articles Aging is a negative regulator of general homeostasis, tissue function, and regeneration. Changes in organismal energy levels and physiology, through systemic manipulations such as calorie restriction and young blood infusion, can regenerate tissue activity and increase lifespan in aged mice. However, whether these two systemic manipulations could be linked has never been investigated. Here, we report that systemic GDF11 triggers a calorie restriction‐like phenotype without affecting appetite or GDF15 levels in the blood, restores the insulin/IGF‐1 signaling pathway, and stimulates adiponectin secretion from white adipose tissue by direct action on adipocytes, while repairing neurogenesis in the aged brain. These findings suggest that GDF11 has a pleiotropic effect on an organismal level and that it could be a linking mechanism of rejuvenation between heterochronic parabiosis and calorie restriction. As such, GDF11 could be considered as an important therapeutic candidate for age‐related neurodegenerative and metabolic disorders. John Wiley and Sons Inc. 2019-10-22 2020-01 /pmc/articles/PMC6974718/ /pubmed/31637864 http://dx.doi.org/10.1111/acel.13038 Text en © 2019 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 Articles Katsimpardi, Lida Kuperwasser, Nicolas Camus, Claire Moigneu, Carine Chiche, Aurélie Tolle, Virginie Li, Han Kokovay, Erzsebet Lledo, Pierre‐Marie Systemic GDF11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice |
title | Systemic GDF11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice |
title_full | Systemic GDF11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice |
title_fullStr | Systemic GDF11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice |
title_full_unstemmed | Systemic GDF11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice |
title_short | Systemic GDF11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice |
title_sort | systemic gdf11 stimulates the secretion of adiponectin and induces a calorie restriction‐like phenotype in aged mice |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974718/ https://www.ncbi.nlm.nih.gov/pubmed/31637864 http://dx.doi.org/10.1111/acel.13038 |
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