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Reproductive Suicide: Similar Mechanisms of Aging in C. elegans and Pacific Salmon
In some species of salmon, reproductive maturity triggers the development of massive pathology resulting from reproductive effort, leading to rapid post-reproductive death. Such reproductive death, which occurs in many semelparous organisms (with a single bout of reproduction), can be prevented by b...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430333/ https://www.ncbi.nlm.nih.gov/pubmed/34513830 http://dx.doi.org/10.3389/fcell.2021.688788 |
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author | Gems, David Kern, Carina C. Nour, Joseph Ezcurra, Marina |
author_facet | Gems, David Kern, Carina C. Nour, Joseph Ezcurra, Marina |
author_sort | Gems, David |
collection | PubMed |
description | In some species of salmon, reproductive maturity triggers the development of massive pathology resulting from reproductive effort, leading to rapid post-reproductive death. Such reproductive death, which occurs in many semelparous organisms (with a single bout of reproduction), can be prevented by blocking reproductive maturation, and this can increase lifespan dramatically. Reproductive death is often viewed as distinct from senescence in iteroparous organisms (with multiple bouts of reproduction) such as humans. Here we review the evidence that reproductive death occurs in C. elegans and discuss what this means for its use as a model organism to study aging. Inhibiting insulin/IGF-1 signaling and germline removal suppresses reproductive death and greatly extends lifespan in C. elegans, but can also extend lifespan to a small extent in iteroparous organisms. We argue that mechanisms of senescence operative in reproductive death exist in a less catastrophic form in iteroparous organisms, particularly those that involve costly resource reallocation, and exhibit endocrine-regulated plasticity. Thus, mechanisms of senescence in semelparous organisms (including plants) and iteroparous ones form an etiological continuum. Therefore understanding mechanisms of reproductive death in C. elegans can teach us about some mechanisms of senescence that are operative in iteroparous organisms. |
format | Online Article Text |
id | pubmed-8430333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84303332021-09-11 Reproductive Suicide: Similar Mechanisms of Aging in C. elegans and Pacific Salmon Gems, David Kern, Carina C. Nour, Joseph Ezcurra, Marina Front Cell Dev Biol Cell and Developmental Biology In some species of salmon, reproductive maturity triggers the development of massive pathology resulting from reproductive effort, leading to rapid post-reproductive death. Such reproductive death, which occurs in many semelparous organisms (with a single bout of reproduction), can be prevented by blocking reproductive maturation, and this can increase lifespan dramatically. Reproductive death is often viewed as distinct from senescence in iteroparous organisms (with multiple bouts of reproduction) such as humans. Here we review the evidence that reproductive death occurs in C. elegans and discuss what this means for its use as a model organism to study aging. Inhibiting insulin/IGF-1 signaling and germline removal suppresses reproductive death and greatly extends lifespan in C. elegans, but can also extend lifespan to a small extent in iteroparous organisms. We argue that mechanisms of senescence operative in reproductive death exist in a less catastrophic form in iteroparous organisms, particularly those that involve costly resource reallocation, and exhibit endocrine-regulated plasticity. Thus, mechanisms of senescence in semelparous organisms (including plants) and iteroparous ones form an etiological continuum. Therefore understanding mechanisms of reproductive death in C. elegans can teach us about some mechanisms of senescence that are operative in iteroparous organisms. Frontiers Media S.A. 2021-08-27 /pmc/articles/PMC8430333/ /pubmed/34513830 http://dx.doi.org/10.3389/fcell.2021.688788 Text en Copyright © 2021 Gems, Kern, Nour and Ezcurra. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Gems, David Kern, Carina C. Nour, Joseph Ezcurra, Marina Reproductive Suicide: Similar Mechanisms of Aging in C. elegans and Pacific Salmon |
title | Reproductive Suicide: Similar Mechanisms of Aging in C. elegans and Pacific Salmon |
title_full | Reproductive Suicide: Similar Mechanisms of Aging in C. elegans and Pacific Salmon |
title_fullStr | Reproductive Suicide: Similar Mechanisms of Aging in C. elegans and Pacific Salmon |
title_full_unstemmed | Reproductive Suicide: Similar Mechanisms of Aging in C. elegans and Pacific Salmon |
title_short | Reproductive Suicide: Similar Mechanisms of Aging in C. elegans and Pacific Salmon |
title_sort | reproductive suicide: similar mechanisms of aging in c. elegans and pacific salmon |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430333/ https://www.ncbi.nlm.nih.gov/pubmed/34513830 http://dx.doi.org/10.3389/fcell.2021.688788 |
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