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C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation
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Title
C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation
Issued Date
2015-11
Citation
Hahm, Jeong-Hoon. (2015-11). C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation. Nature Communications, 6. doi: 10.1038/ncomms9919
Type
Article
Keywords
AGE-RELATED-CHANGESAgingArticleCAENORHABDITIS-ELEGANSCaenorhabditis ElegansControlled StudyDAF-16Food IntakeGene ExpressionGene MutationGENETIC-ANALYSISGenetic AnalysisGenetic VariationHormoneInsulin ReceptorLIFE-SPANLife ExtensionLifespanLONGEVITYMITOCHONDRIALMOTOR-ACTIVITY DECLINEMovementMUTANTSMutationNematodeNERVOUS-systemNonhumanPeptidePhysical CapacityPhysical PerformanceSignal TransductionSomatomedin CWILD-TYPE
ISSN
2041-1723
Abstract
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. © 2015 Macmillan Publishers Limited. All rights reserved.
URI
http://hdl.handle.net/20.500.11750/1562
DOI
10.1038/ncomms9919
Publisher
NATURE PUBLISHING GROUP
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