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IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice
Advanced maternal-age is a major factor adversely affecting oocyte quality, consequently worsening pregnancy outcomes. Thus, developing strategies to reduce the developmental defects associated with advanced maternal-age would benefit older mothers. Multiple growth factors involved in female fertili...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880328/ https://www.ncbi.nlm.nih.gov/pubmed/33318299 http://dx.doi.org/10.18632/aging.202214 |
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author | Muhammad, Tahir Wan, Yanling Sha, Qianqian Wang, Jianfeng Huang, Tao Cao, Yongzhi Li, Mengjing Yu, Xiaochen Yin, Yingying Chan, Wai Yee Chen, Zi-Jiang You, Li Lu, Gang Liu, Hongbin |
author_facet | Muhammad, Tahir Wan, Yanling Sha, Qianqian Wang, Jianfeng Huang, Tao Cao, Yongzhi Li, Mengjing Yu, Xiaochen Yin, Yingying Chan, Wai Yee Chen, Zi-Jiang You, Li Lu, Gang Liu, Hongbin |
author_sort | Muhammad, Tahir |
collection | PubMed |
description | Advanced maternal-age is a major factor adversely affecting oocyte quality, consequently worsening pregnancy outcomes. Thus, developing strategies to reduce the developmental defects associated with advanced maternal-age would benefit older mothers. Multiple growth factors involved in female fertility have been extensively studied; however, the age-related impacts of various growth factors remain poorly studied. In the present study, we identified that levels of insulin-like growth factor 2 (IGF2) are significantly reduced in the serum and oocytes of aged mice. We found that adding IGF2 in culture medium promotes oocyte maturation and significantly increases the proportion of blastocysts: from 41% in the untreated control group to 64% (50 nM IGF2) in aged mice (p < 0.05). Additionally, IGF2 supplementation of the culture medium reduced reactive oxygen species production and the incidence of spindle/chromosome defects. IGF2 increases mitochondrial functional activity in oocytes from aged mice: we detected increased ATP levels, elevated fluorescence intensity of mitochondria, higher mitochondrial membrane potentials, and increased overall protein synthesis, as well as increased autophagy activity and decreased apoptosis. Collectively, our findings demonstrate that IGF2 supplementation in culture media improves oocyte developmental competence and reduces meiotic structure defects in oocytes from aged mice. |
format | Online Article Text |
id | pubmed-7880328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-78803282021-02-22 IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice Muhammad, Tahir Wan, Yanling Sha, Qianqian Wang, Jianfeng Huang, Tao Cao, Yongzhi Li, Mengjing Yu, Xiaochen Yin, Yingying Chan, Wai Yee Chen, Zi-Jiang You, Li Lu, Gang Liu, Hongbin Aging (Albany NY) Research Paper Advanced maternal-age is a major factor adversely affecting oocyte quality, consequently worsening pregnancy outcomes. Thus, developing strategies to reduce the developmental defects associated with advanced maternal-age would benefit older mothers. Multiple growth factors involved in female fertility have been extensively studied; however, the age-related impacts of various growth factors remain poorly studied. In the present study, we identified that levels of insulin-like growth factor 2 (IGF2) are significantly reduced in the serum and oocytes of aged mice. We found that adding IGF2 in culture medium promotes oocyte maturation and significantly increases the proportion of blastocysts: from 41% in the untreated control group to 64% (50 nM IGF2) in aged mice (p < 0.05). Additionally, IGF2 supplementation of the culture medium reduced reactive oxygen species production and the incidence of spindle/chromosome defects. IGF2 increases mitochondrial functional activity in oocytes from aged mice: we detected increased ATP levels, elevated fluorescence intensity of mitochondria, higher mitochondrial membrane potentials, and increased overall protein synthesis, as well as increased autophagy activity and decreased apoptosis. Collectively, our findings demonstrate that IGF2 supplementation in culture media improves oocyte developmental competence and reduces meiotic structure defects in oocytes from aged mice. Impact Journals 2020-12-09 /pmc/articles/PMC7880328/ /pubmed/33318299 http://dx.doi.org/10.18632/aging.202214 Text en Copyright: © 2021 Muhammad et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Muhammad, Tahir Wan, Yanling Sha, Qianqian Wang, Jianfeng Huang, Tao Cao, Yongzhi Li, Mengjing Yu, Xiaochen Yin, Yingying Chan, Wai Yee Chen, Zi-Jiang You, Li Lu, Gang Liu, Hongbin IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice |
title | IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice |
title_full | IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice |
title_fullStr | IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice |
title_full_unstemmed | IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice |
title_short | IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice |
title_sort | igf2 improves the developmental competency and meiotic structure of oocytes from aged mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880328/ https://www.ncbi.nlm.nih.gov/pubmed/33318299 http://dx.doi.org/10.18632/aging.202214 |
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