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Regulation of the one carbon folate cycle as a shared metabolic signature of longevity
The metabolome represents a complex network of biological events that reflects the physiologic state of the organism in health and disease. Additionally, specific metabolites and metabolic signaling pathways have been shown to modulate animal ageing, but whether there are convergent mechanisms uniti...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190293/ https://www.ncbi.nlm.nih.gov/pubmed/34108489 http://dx.doi.org/10.1038/s41467-021-23856-9 |
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author | Annibal, Andrea Tharyan, Rebecca George Schonewolff, Maribel Fides Tam, Hannah Latza, Christian Auler, Markus Max Karl Grönke, Sebastian Partridge, Linda Antebi, Adam |
author_facet | Annibal, Andrea Tharyan, Rebecca George Schonewolff, Maribel Fides Tam, Hannah Latza, Christian Auler, Markus Max Karl Grönke, Sebastian Partridge, Linda Antebi, Adam |
author_sort | Annibal, Andrea |
collection | PubMed |
description | The metabolome represents a complex network of biological events that reflects the physiologic state of the organism in health and disease. Additionally, specific metabolites and metabolic signaling pathways have been shown to modulate animal ageing, but whether there are convergent mechanisms uniting these processes remains elusive. Here, we used high resolution mass spectrometry to obtain the metabolomic profiles of canonical longevity pathways in C. elegans to identify metabolites regulating life span. By leveraging the metabolomic profiles across pathways, we found that one carbon metabolism and the folate cycle are pervasively regulated in common. We observed similar changes in long-lived mouse models of reduced insulin/IGF signaling. Genetic manipulation of pathway enzymes and supplementation with one carbon metabolites in C. elegans reveal that regulation of the folate cycle represents a shared causal mechanism of longevity and proteoprotection. Such interventions impact the methionine cycle, and reveal methionine restriction as an underlying mechanism. This comparative approach reveals key metabolic nodes to enhance healthy ageing. |
format | Online Article Text |
id | pubmed-8190293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81902932021-07-01 Regulation of the one carbon folate cycle as a shared metabolic signature of longevity Annibal, Andrea Tharyan, Rebecca George Schonewolff, Maribel Fides Tam, Hannah Latza, Christian Auler, Markus Max Karl Grönke, Sebastian Partridge, Linda Antebi, Adam Nat Commun Article The metabolome represents a complex network of biological events that reflects the physiologic state of the organism in health and disease. Additionally, specific metabolites and metabolic signaling pathways have been shown to modulate animal ageing, but whether there are convergent mechanisms uniting these processes remains elusive. Here, we used high resolution mass spectrometry to obtain the metabolomic profiles of canonical longevity pathways in C. elegans to identify metabolites regulating life span. By leveraging the metabolomic profiles across pathways, we found that one carbon metabolism and the folate cycle are pervasively regulated in common. We observed similar changes in long-lived mouse models of reduced insulin/IGF signaling. Genetic manipulation of pathway enzymes and supplementation with one carbon metabolites in C. elegans reveal that regulation of the folate cycle represents a shared causal mechanism of longevity and proteoprotection. Such interventions impact the methionine cycle, and reveal methionine restriction as an underlying mechanism. This comparative approach reveals key metabolic nodes to enhance healthy ageing. Nature Publishing Group UK 2021-06-09 /pmc/articles/PMC8190293/ /pubmed/34108489 http://dx.doi.org/10.1038/s41467-021-23856-9 Text en © The Author(s) 2021, corrected publication 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Annibal, Andrea Tharyan, Rebecca George Schonewolff, Maribel Fides Tam, Hannah Latza, Christian Auler, Markus Max Karl Grönke, Sebastian Partridge, Linda Antebi, Adam Regulation of the one carbon folate cycle as a shared metabolic signature of longevity |
title | Regulation of the one carbon folate cycle as a shared metabolic signature of longevity |
title_full | Regulation of the one carbon folate cycle as a shared metabolic signature of longevity |
title_fullStr | Regulation of the one carbon folate cycle as a shared metabolic signature of longevity |
title_full_unstemmed | Regulation of the one carbon folate cycle as a shared metabolic signature of longevity |
title_short | Regulation of the one carbon folate cycle as a shared metabolic signature of longevity |
title_sort | regulation of the one carbon folate cycle as a shared metabolic signature of longevity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190293/ https://www.ncbi.nlm.nih.gov/pubmed/34108489 http://dx.doi.org/10.1038/s41467-021-23856-9 |
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