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Greater loss of mitochondrial function with ageing is associated with earlier onset of sarcopenia in C. elegans
Sarcopenia, the age-related decline of muscle, is a significant and growing public health burden. C. elegans, a model organism for investigating the mechanisms of ageing, also displays sarcopenia, but the underlying mechanism(s) remain elusive. Here, we use C. elegans natural scaling of lifespan in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286836/ https://www.ncbi.nlm.nih.gov/pubmed/30455409 http://dx.doi.org/10.18632/aging.101654 |
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author | Gaffney, Christopher J. Pollard, Amelia Barratt, Thomas F. Constantin-Teodosiu, Dumitru Greenhaff, Paul L. Szewczyk, Nathaniel J. |
author_facet | Gaffney, Christopher J. Pollard, Amelia Barratt, Thomas F. Constantin-Teodosiu, Dumitru Greenhaff, Paul L. Szewczyk, Nathaniel J. |
author_sort | Gaffney, Christopher J. |
collection | PubMed |
description | Sarcopenia, the age-related decline of muscle, is a significant and growing public health burden. C. elegans, a model organism for investigating the mechanisms of ageing, also displays sarcopenia, but the underlying mechanism(s) remain elusive. Here, we use C. elegans natural scaling of lifespan in response to temperature to examine the relationship between mitochondrial content, mitochondrial function, and sarcopenia. Mitochondrial content and maximal mitochondrial ATP production rates (MAPR) display an inverse relationship to lifespan, while onset of MAPR decline displays a direct relationship. Muscle mitochondrial structure, sarcomere structure, and movement decline also display a direct relationship with longevity. Notably, the decline in mitochondrial network structure occurs earlier than sarcomere decline, and correlates more strongly with loss of movement, and scales with lifespan. These results suggest that mitochondrial function is critical in the ageing process and more robustly explains the onset and progression of sarcopenia than loss of sarcomere structure. |
format | Online Article Text |
id | pubmed-6286836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-62868362018-12-17 Greater loss of mitochondrial function with ageing is associated with earlier onset of sarcopenia in C. elegans Gaffney, Christopher J. Pollard, Amelia Barratt, Thomas F. Constantin-Teodosiu, Dumitru Greenhaff, Paul L. Szewczyk, Nathaniel J. Aging (Albany NY) Research Paper Sarcopenia, the age-related decline of muscle, is a significant and growing public health burden. C. elegans, a model organism for investigating the mechanisms of ageing, also displays sarcopenia, but the underlying mechanism(s) remain elusive. Here, we use C. elegans natural scaling of lifespan in response to temperature to examine the relationship between mitochondrial content, mitochondrial function, and sarcopenia. Mitochondrial content and maximal mitochondrial ATP production rates (MAPR) display an inverse relationship to lifespan, while onset of MAPR decline displays a direct relationship. Muscle mitochondrial structure, sarcomere structure, and movement decline also display a direct relationship with longevity. Notably, the decline in mitochondrial network structure occurs earlier than sarcomere decline, and correlates more strongly with loss of movement, and scales with lifespan. These results suggest that mitochondrial function is critical in the ageing process and more robustly explains the onset and progression of sarcopenia than loss of sarcomere structure. Impact Journals 2018-11-19 /pmc/articles/PMC6286836/ /pubmed/30455409 http://dx.doi.org/10.18632/aging.101654 Text en Copyright © 2018 Gaffney et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Gaffney, Christopher J. Pollard, Amelia Barratt, Thomas F. Constantin-Teodosiu, Dumitru Greenhaff, Paul L. Szewczyk, Nathaniel J. Greater loss of mitochondrial function with ageing is associated with earlier onset of sarcopenia in C. elegans |
title | Greater loss of mitochondrial function with ageing is associated with earlier onset of sarcopenia in C. elegans |
title_full | Greater loss of mitochondrial function with ageing is associated with earlier onset of sarcopenia in C. elegans |
title_fullStr | Greater loss of mitochondrial function with ageing is associated with earlier onset of sarcopenia in C. elegans |
title_full_unstemmed | Greater loss of mitochondrial function with ageing is associated with earlier onset of sarcopenia in C. elegans |
title_short | Greater loss of mitochondrial function with ageing is associated with earlier onset of sarcopenia in C. elegans |
title_sort | greater loss of mitochondrial function with ageing is associated with earlier onset of sarcopenia in c. elegans |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286836/ https://www.ncbi.nlm.nih.gov/pubmed/30455409 http://dx.doi.org/10.18632/aging.101654 |
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