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Calorie restriction does not influence oocyte quality in oocytes from POLG mitochondrial mutator mice
It has recently been demonstrated that moderate adult onset caloric restriction (e.g. calorie restriction; CR) has a positive impact on female fertility in aged mice, due in large to preventing the age-associated decline in the quality of oocytes available for fertilization. The impact of CR on oocy...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150528/ https://www.ncbi.nlm.nih.gov/pubmed/30240410 http://dx.doi.org/10.1371/journal.pone.0204373 |
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author | Faraci, Christine Jin, Joyce Woods, Dori C. |
author_facet | Faraci, Christine Jin, Joyce Woods, Dori C. |
author_sort | Faraci, Christine |
collection | PubMed |
description | It has recently been demonstrated that moderate adult onset caloric restriction (e.g. calorie restriction; CR) has a positive impact on female fertility in aged mice, due in large to preventing the age-associated decline in the quality of oocytes available for fertilization. The impact of CR on oocyte quality has been attributed, at least in part, to mitochondrial functions. In mitochondrial DNA (mtDNA) mutator mice (Polg(D257A/D257A)), which harbor a mutation in the proofreading mtDNA polymerase-gamma (POLG), mitochondrial mutations rapidly accumulate, resulting in a premature aging phenotype and female infertility. As CR has been shown to extend both lifespan and ‘healthspan’ as well as improve oocyte quality in aged mice, we investigated whether adult onset CR could improve oocyte quality in the POLG mouse. Female Polg(D257A/D257A) mice exhibited infertility based on an inability to produce litters through natural mating. Analysis of oocytes from 8–9-month-old Polg(D257A/D257A) mice on CR following hormone stimulation revealed no improvement in the number of oocytes ovulated. Furthermore, CR did not result in a greater percentage of metaphase II oocytes, with the majority of the oocytes prematurely arrested at the germinal vesicle stage. Finally, CR did not improve the abnormal mitochondrial distribution or pronounced defects in meiotic spindle assembly and chromosomal distribution observed in the ad libitum fed Polg(D257A/D257A). Taken together, these data suggest that although CR benefits oocyte quality and fertility outcomes in naturally aged female mice, it does not sufficiently improve oocyte quality in Polg(D257A/D257A). |
format | Online Article Text |
id | pubmed-6150528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61505282018-10-08 Calorie restriction does not influence oocyte quality in oocytes from POLG mitochondrial mutator mice Faraci, Christine Jin, Joyce Woods, Dori C. PLoS One Research Article It has recently been demonstrated that moderate adult onset caloric restriction (e.g. calorie restriction; CR) has a positive impact on female fertility in aged mice, due in large to preventing the age-associated decline in the quality of oocytes available for fertilization. The impact of CR on oocyte quality has been attributed, at least in part, to mitochondrial functions. In mitochondrial DNA (mtDNA) mutator mice (Polg(D257A/D257A)), which harbor a mutation in the proofreading mtDNA polymerase-gamma (POLG), mitochondrial mutations rapidly accumulate, resulting in a premature aging phenotype and female infertility. As CR has been shown to extend both lifespan and ‘healthspan’ as well as improve oocyte quality in aged mice, we investigated whether adult onset CR could improve oocyte quality in the POLG mouse. Female Polg(D257A/D257A) mice exhibited infertility based on an inability to produce litters through natural mating. Analysis of oocytes from 8–9-month-old Polg(D257A/D257A) mice on CR following hormone stimulation revealed no improvement in the number of oocytes ovulated. Furthermore, CR did not result in a greater percentage of metaphase II oocytes, with the majority of the oocytes prematurely arrested at the germinal vesicle stage. Finally, CR did not improve the abnormal mitochondrial distribution or pronounced defects in meiotic spindle assembly and chromosomal distribution observed in the ad libitum fed Polg(D257A/D257A). Taken together, these data suggest that although CR benefits oocyte quality and fertility outcomes in naturally aged female mice, it does not sufficiently improve oocyte quality in Polg(D257A/D257A). Public Library of Science 2018-09-21 /pmc/articles/PMC6150528/ /pubmed/30240410 http://dx.doi.org/10.1371/journal.pone.0204373 Text en © 2018 Faraci et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Faraci, Christine Jin, Joyce Woods, Dori C. Calorie restriction does not influence oocyte quality in oocytes from POLG mitochondrial mutator mice |
title | Calorie restriction does not influence oocyte quality in oocytes from POLG mitochondrial mutator mice |
title_full | Calorie restriction does not influence oocyte quality in oocytes from POLG mitochondrial mutator mice |
title_fullStr | Calorie restriction does not influence oocyte quality in oocytes from POLG mitochondrial mutator mice |
title_full_unstemmed | Calorie restriction does not influence oocyte quality in oocytes from POLG mitochondrial mutator mice |
title_short | Calorie restriction does not influence oocyte quality in oocytes from POLG mitochondrial mutator mice |
title_sort | calorie restriction does not influence oocyte quality in oocytes from polg mitochondrial mutator mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150528/ https://www.ncbi.nlm.nih.gov/pubmed/30240410 http://dx.doi.org/10.1371/journal.pone.0204373 |
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