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Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegans
Deregulated energy homeostasis represents a hallmark of aging and results from complex gene-by-environment interactions. Here, we discovered that reducing the expression of the gene ech-6 encoding enoyl-CoA hydratase remitted fat diet-induced deleterious effects on lifespan in Caenorhabditis elegans...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888598/ https://www.ncbi.nlm.nih.gov/pubmed/35233004 http://dx.doi.org/10.1038/s41598-022-07397-9 |
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author | Liu, Yasmine J. Gao, Arwen W. Smith, Reuben L. Janssens, Georges E. Panneman, Daan M. Jongejan, Aldo van Weeghel, Michel Vaz, Frédéric M. Silvestrini, Melissa J. Lapierre, Louis R. MacInnes, Alyson W. Houtkooper, Riekelt H. |
author_facet | Liu, Yasmine J. Gao, Arwen W. Smith, Reuben L. Janssens, Georges E. Panneman, Daan M. Jongejan, Aldo van Weeghel, Michel Vaz, Frédéric M. Silvestrini, Melissa J. Lapierre, Louis R. MacInnes, Alyson W. Houtkooper, Riekelt H. |
author_sort | Liu, Yasmine J. |
collection | PubMed |
description | Deregulated energy homeostasis represents a hallmark of aging and results from complex gene-by-environment interactions. Here, we discovered that reducing the expression of the gene ech-6 encoding enoyl-CoA hydratase remitted fat diet-induced deleterious effects on lifespan in Caenorhabditis elegans, while a basal expression of ech-6 was important for survival under normal dietary conditions. Lipidomics revealed that supplementation of fat in ech-6-silenced worms had marginal effects on lipid profiles, suggesting an alternative fat utilization for energy production. Transcriptomics further suggest a causal relation between the lysosomal pathway, energy production, and the longevity effect conferred by the interaction between ech-6 and fat diets. Indeed, enhancing energy production from endogenous fat by overexpressing lysosomal lipase lipl-4 recapitulated the lifespan effects of fat diets on ech-6-silenced worms. Collectively, these results suggest that the gene ech-6 is potential modulator of metabolic flexibility and may be a target for promoting metabolic health and longevity. |
format | Online Article Text |
id | pubmed-8888598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88885982022-03-03 Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegans Liu, Yasmine J. Gao, Arwen W. Smith, Reuben L. Janssens, Georges E. Panneman, Daan M. Jongejan, Aldo van Weeghel, Michel Vaz, Frédéric M. Silvestrini, Melissa J. Lapierre, Louis R. MacInnes, Alyson W. Houtkooper, Riekelt H. Sci Rep Article Deregulated energy homeostasis represents a hallmark of aging and results from complex gene-by-environment interactions. Here, we discovered that reducing the expression of the gene ech-6 encoding enoyl-CoA hydratase remitted fat diet-induced deleterious effects on lifespan in Caenorhabditis elegans, while a basal expression of ech-6 was important for survival under normal dietary conditions. Lipidomics revealed that supplementation of fat in ech-6-silenced worms had marginal effects on lipid profiles, suggesting an alternative fat utilization for energy production. Transcriptomics further suggest a causal relation between the lysosomal pathway, energy production, and the longevity effect conferred by the interaction between ech-6 and fat diets. Indeed, enhancing energy production from endogenous fat by overexpressing lysosomal lipase lipl-4 recapitulated the lifespan effects of fat diets on ech-6-silenced worms. Collectively, these results suggest that the gene ech-6 is potential modulator of metabolic flexibility and may be a target for promoting metabolic health and longevity. Nature Publishing Group UK 2022-03-01 /pmc/articles/PMC8888598/ /pubmed/35233004 http://dx.doi.org/10.1038/s41598-022-07397-9 Text en © The Author(s) 2022 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/) . |
spellingShingle | Article Liu, Yasmine J. Gao, Arwen W. Smith, Reuben L. Janssens, Georges E. Panneman, Daan M. Jongejan, Aldo van Weeghel, Michel Vaz, Frédéric M. Silvestrini, Melissa J. Lapierre, Louis R. MacInnes, Alyson W. Houtkooper, Riekelt H. Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegans |
title | Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegans |
title_full | Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegans |
title_fullStr | Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegans |
title_full_unstemmed | Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegans |
title_short | Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegans |
title_sort | reduced ech-6 expression attenuates fat-induced lifespan shortening in c. elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888598/ https://www.ncbi.nlm.nih.gov/pubmed/35233004 http://dx.doi.org/10.1038/s41598-022-07397-9 |
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