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Telomere length declines with age, but relates to immune function independent of age in a wild passerine

Telomere length (TL) shortens with age but telomere dynamics can relate to fitness components independent of age. Immune function often relates to such fitness components and can also interact with telomeres. Studying the link between TL and immune function may therefore help us understand telomere–...

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Autores principales: Roast, Michael J., Eastwood, Justin R., Aranzamendi, Nataly Hidalgo, Fan, Marie, Teunissen, Niki, Verhulst, Simon, Peters, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043702/
https://www.ncbi.nlm.nih.gov/pubmed/35601455
http://dx.doi.org/10.1098/rsos.212012
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author Roast, Michael J.
Eastwood, Justin R.
Aranzamendi, Nataly Hidalgo
Fan, Marie
Teunissen, Niki
Verhulst, Simon
Peters, Anne
author_facet Roast, Michael J.
Eastwood, Justin R.
Aranzamendi, Nataly Hidalgo
Fan, Marie
Teunissen, Niki
Verhulst, Simon
Peters, Anne
author_sort Roast, Michael J.
collection PubMed
description Telomere length (TL) shortens with age but telomere dynamics can relate to fitness components independent of age. Immune function often relates to such fitness components and can also interact with telomeres. Studying the link between TL and immune function may therefore help us understand telomere–fitness associations. We assessed the relationships between erythrocyte TL and four immune indices (haptoglobin, natural antibodies (NAbs), complement activity (CA) and heterophil-lymphocyte (HL) ratio; n = 477–589), from known-aged individuals of a wild passerine (Malurus coronatus). As expected, we find that TL significantly declined with age. To verify whether associations between TL and immune function were independent of parallel age-related changes (e.g. immunosenescence), we statistically controlled for sampling age and used within-subject centring of TL to separate relationships within or between individuals. We found that TL positively predicted CA at the between-individual level (individuals with longer average TL had higher CA), but no other immune indices. By contrast, age predicted the levels of NAbs and HL ratio, allowing inference that respective associations between TL and age with immune indices are independent. Any links existing between TL and fitness are therefore unlikely to be strongly mediated by innate immune function, while TL and immune indices appear independent expressions of individual heterogeneity.
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spelling pubmed-90437022022-05-21 Telomere length declines with age, but relates to immune function independent of age in a wild passerine Roast, Michael J. Eastwood, Justin R. Aranzamendi, Nataly Hidalgo Fan, Marie Teunissen, Niki Verhulst, Simon Peters, Anne R Soc Open Sci Organismal and Evolutionary Biology Telomere length (TL) shortens with age but telomere dynamics can relate to fitness components independent of age. Immune function often relates to such fitness components and can also interact with telomeres. Studying the link between TL and immune function may therefore help us understand telomere–fitness associations. We assessed the relationships between erythrocyte TL and four immune indices (haptoglobin, natural antibodies (NAbs), complement activity (CA) and heterophil-lymphocyte (HL) ratio; n = 477–589), from known-aged individuals of a wild passerine (Malurus coronatus). As expected, we find that TL significantly declined with age. To verify whether associations between TL and immune function were independent of parallel age-related changes (e.g. immunosenescence), we statistically controlled for sampling age and used within-subject centring of TL to separate relationships within or between individuals. We found that TL positively predicted CA at the between-individual level (individuals with longer average TL had higher CA), but no other immune indices. By contrast, age predicted the levels of NAbs and HL ratio, allowing inference that respective associations between TL and age with immune indices are independent. Any links existing between TL and fitness are therefore unlikely to be strongly mediated by innate immune function, while TL and immune indices appear independent expressions of individual heterogeneity. The Royal Society 2022-04-27 /pmc/articles/PMC9043702/ /pubmed/35601455 http://dx.doi.org/10.1098/rsos.212012 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Organismal and Evolutionary Biology
Roast, Michael J.
Eastwood, Justin R.
Aranzamendi, Nataly Hidalgo
Fan, Marie
Teunissen, Niki
Verhulst, Simon
Peters, Anne
Telomere length declines with age, but relates to immune function independent of age in a wild passerine
title Telomere length declines with age, but relates to immune function independent of age in a wild passerine
title_full Telomere length declines with age, but relates to immune function independent of age in a wild passerine
title_fullStr Telomere length declines with age, but relates to immune function independent of age in a wild passerine
title_full_unstemmed Telomere length declines with age, but relates to immune function independent of age in a wild passerine
title_short Telomere length declines with age, but relates to immune function independent of age in a wild passerine
title_sort telomere length declines with age, but relates to immune function independent of age in a wild passerine
topic Organismal and Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043702/
https://www.ncbi.nlm.nih.gov/pubmed/35601455
http://dx.doi.org/10.1098/rsos.212012
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