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C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation
Ageing is marked by physical decline. Caenorhabditis elegans is a valuable model for identifying genetic regulatory mechanisms of ageing and longevity. Here we report a simple method to assess C. elegans' maximum physical ability based on the worms' maximum movement velocity. We show maxim...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4656132/ https://www.ncbi.nlm.nih.gov/pubmed/26586186 http://dx.doi.org/10.1038/ncomms9919 |
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author | Hahm, Jeong-Hoon Kim, Sunhee DiLoreto, Race Shi, Cheng Lee, Seung-Jae V. Murphy, Coleen T. Nam, Hong Gil |
author_facet | Hahm, Jeong-Hoon Kim, Sunhee DiLoreto, Race Shi, Cheng Lee, Seung-Jae V. Murphy, Coleen T. Nam, Hong Gil |
author_sort | Hahm, Jeong-Hoon |
collection | PubMed |
description | Ageing is marked by physical decline. Caenorhabditis elegans is a valuable model for identifying genetic regulatory mechanisms of ageing and longevity. Here we report a simple method to assess C. elegans' maximum physical ability based on the worms' maximum movement velocity. We show maximum velocity declines with age, correlates well with longevity, accurately reports movement ability and, if measured in mid-adulthood, is predictive of maximal lifespan. Contrary to recent findings, we observe that maximum velocity of worm with mutations in daf-2(e1370) insulin/IGF-1 signalling scales with lifespan. Because of increased odorant receptor expression, daf-2(e1370) mutants prefer food over exploration, causing previous on-food motility assays to underestimate movement ability and, thus, worm health. Finally, a disease-burden analysis of published data reveals that the daf-2(e1370) mutation improves quality of life, and therefore combines lifespan extension with various signs of an increased healthspan. |
format | Online Article Text |
id | pubmed-4656132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46561322015-12-17 C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation Hahm, Jeong-Hoon Kim, Sunhee DiLoreto, Race Shi, Cheng Lee, Seung-Jae V. Murphy, Coleen T. Nam, Hong Gil Nat Commun Article Ageing is marked by physical decline. Caenorhabditis elegans is a valuable model for identifying genetic regulatory mechanisms of ageing and longevity. Here we report a simple method to assess C. elegans' maximum physical ability based on the worms' maximum movement velocity. We show maximum velocity declines with age, correlates well with longevity, accurately reports movement ability and, if measured in mid-adulthood, is predictive of maximal lifespan. Contrary to recent findings, we observe that maximum velocity of worm with mutations in daf-2(e1370) insulin/IGF-1 signalling scales with lifespan. Because of increased odorant receptor expression, daf-2(e1370) mutants prefer food over exploration, causing previous on-food motility assays to underestimate movement ability and, thus, worm health. Finally, a disease-burden analysis of published data reveals that the daf-2(e1370) mutation improves quality of life, and therefore combines lifespan extension with various signs of an increased healthspan. Nature Pub. Group 2015-11-20 /pmc/articles/PMC4656132/ /pubmed/26586186 http://dx.doi.org/10.1038/ncomms9919 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hahm, Jeong-Hoon Kim, Sunhee DiLoreto, Race Shi, Cheng Lee, Seung-Jae V. Murphy, Coleen T. Nam, Hong Gil C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation |
title | C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation |
title_full | C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation |
title_fullStr | C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation |
title_full_unstemmed | C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation |
title_short | C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation |
title_sort | c. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4656132/ https://www.ncbi.nlm.nih.gov/pubmed/26586186 http://dx.doi.org/10.1038/ncomms9919 |
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