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Mitochondrial membrane lipidome defines yeast longevity
Our studies revealed that lithocholic acid (LCA), a bile acid, is a potent anti-aging natural compound that in yeast cultured under longevity-extending caloric restriction (CR) conditions acts in synergy with CR to enable a significant further increase in chronological lifespan. Here, we investigate...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765583/ https://www.ncbi.nlm.nih.gov/pubmed/23924582 |
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author | Beach, Adam Richard, Vincent R. Leonov, Anna Burstein, Michelle T. Bourque, Simon D. Koupaki, Olivia Juneau, Mylène Feldman, Rachel Iouk, Tatiana Titorenko, Vladimir I. |
author_facet | Beach, Adam Richard, Vincent R. Leonov, Anna Burstein, Michelle T. Bourque, Simon D. Koupaki, Olivia Juneau, Mylène Feldman, Rachel Iouk, Tatiana Titorenko, Vladimir I. |
author_sort | Beach, Adam |
collection | PubMed |
description | Our studies revealed that lithocholic acid (LCA), a bile acid, is a potent anti-aging natural compound that in yeast cultured under longevity-extending caloric restriction (CR) conditions acts in synergy with CR to enable a significant further increase in chronological lifespan. Here, we investigate a mechanism underlying this robust longevity-extending effect of LCA under CR. We found that exogenously added LCA enters yeast cells, is sorted to mitochondria, resides mainly in the inner mitochondrial membrane, and also associates with the outer mitochondrial membrane. LCA elicits an age-related remodeling of glycerophospholipid synthesis and movement within both mitochondrial membranes, thereby causing substantial changes in mitochondrial membrane lipidome and triggering major changes in mitochondrial size, number and morphology. In synergy, these changes in the membrane lipidome and morphology of mitochondria alter the age-related chronology of mitochondrial respiration, membrane potential, ATP synthesis and reactive oxygen species homeostasis. The LCA-driven alterations in the age-related dynamics of these vital mitochondrial processes extend yeast longevity. In sum, our findings suggest a mechanism underlying the ability of LCA to delay chronological aging in yeast by accumulating in both mitochondrial membranes and altering their glycerophospholipid compositions. We concluded that mitochondrial membrane lipidome plays an essential role in defining yeast longevity. |
format | Online Article Text |
id | pubmed-3765583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-37655832013-09-10 Mitochondrial membrane lipidome defines yeast longevity Beach, Adam Richard, Vincent R. Leonov, Anna Burstein, Michelle T. Bourque, Simon D. Koupaki, Olivia Juneau, Mylène Feldman, Rachel Iouk, Tatiana Titorenko, Vladimir I. Aging (Albany NY) Research Paper Our studies revealed that lithocholic acid (LCA), a bile acid, is a potent anti-aging natural compound that in yeast cultured under longevity-extending caloric restriction (CR) conditions acts in synergy with CR to enable a significant further increase in chronological lifespan. Here, we investigate a mechanism underlying this robust longevity-extending effect of LCA under CR. We found that exogenously added LCA enters yeast cells, is sorted to mitochondria, resides mainly in the inner mitochondrial membrane, and also associates with the outer mitochondrial membrane. LCA elicits an age-related remodeling of glycerophospholipid synthesis and movement within both mitochondrial membranes, thereby causing substantial changes in mitochondrial membrane lipidome and triggering major changes in mitochondrial size, number and morphology. In synergy, these changes in the membrane lipidome and morphology of mitochondria alter the age-related chronology of mitochondrial respiration, membrane potential, ATP synthesis and reactive oxygen species homeostasis. The LCA-driven alterations in the age-related dynamics of these vital mitochondrial processes extend yeast longevity. In sum, our findings suggest a mechanism underlying the ability of LCA to delay chronological aging in yeast by accumulating in both mitochondrial membranes and altering their glycerophospholipid compositions. We concluded that mitochondrial membrane lipidome plays an essential role in defining yeast longevity. Impact Journals LLC 2013-07-18 /pmc/articles/PMC3765583/ /pubmed/23924582 Text en Copyright: © 2013 Beach et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited |
spellingShingle | Research Paper Beach, Adam Richard, Vincent R. Leonov, Anna Burstein, Michelle T. Bourque, Simon D. Koupaki, Olivia Juneau, Mylène Feldman, Rachel Iouk, Tatiana Titorenko, Vladimir I. Mitochondrial membrane lipidome defines yeast longevity |
title | Mitochondrial membrane lipidome defines yeast longevity |
title_full | Mitochondrial membrane lipidome defines yeast longevity |
title_fullStr | Mitochondrial membrane lipidome defines yeast longevity |
title_full_unstemmed | Mitochondrial membrane lipidome defines yeast longevity |
title_short | Mitochondrial membrane lipidome defines yeast longevity |
title_sort | mitochondrial membrane lipidome defines yeast longevity |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765583/ https://www.ncbi.nlm.nih.gov/pubmed/23924582 |
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