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Antioxidant procyanidin B2 protects oocytes against cryoinjuries via mitochondria regulated cortical tension
BACKGROUND: Irreversible cryodamage caused by oocyte vitrification limited its wild application in female fertility preservation. Antioxidants were always used to antagonist the oxidative stress caused by vitrification. However, the comprehensive mechanism underlying the protective role of antioxida...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380387/ https://www.ncbi.nlm.nih.gov/pubmed/35971139 http://dx.doi.org/10.1186/s40104-022-00742-y |
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author | Zhuan, Qingrui Li, Jun Du, Xingzhu Zhang, Luyao Meng, Lin Luo, Yuwen Zhou, Dan Liu, Hongyu Wan, Pengcheng Hou, Yunpeng Fu, Xiangwei |
author_facet | Zhuan, Qingrui Li, Jun Du, Xingzhu Zhang, Luyao Meng, Lin Luo, Yuwen Zhou, Dan Liu, Hongyu Wan, Pengcheng Hou, Yunpeng Fu, Xiangwei |
author_sort | Zhuan, Qingrui |
collection | PubMed |
description | BACKGROUND: Irreversible cryodamage caused by oocyte vitrification limited its wild application in female fertility preservation. Antioxidants were always used to antagonist the oxidative stress caused by vitrification. However, the comprehensive mechanism underlying the protective role of antioxidants has not been studied. Procyanidin B2 (PCB2) is a potent natural antioxidant and its functions in response to vitrification are still unknown. In this study, the effects of PCB2 on vitrified-thawed oocytes and subsequent embryo development were explored, and the mechanisms underlying the protective role of PCB2 were systematically elucidated. RESULTS: Vitrification induced a marked decline in oocyte quality, while PCB2 could improve oocyte viability and further development after parthenogenetic activation. A subsequent study indicated that PCB2 effectively attenuated vitrification-induced oxidative stress, rescued mitochondrial dysfunction, and improved cell viability. Moreover, PCB2 also acts as a cortical tension regulator apart from strong antioxidant properties. Increased cortical tension caused by PCB2 would maintain normal spindle morphology and promote migration, ensure correct meiosis progression and finally reduce the aneuploidy rate in vitrified oocytes. Further study reveals that ATP biosynthesis plays a crucial role in cortical tension regulation, and PCB2 effectively increased the cortical tension through the electron transfer chain pathway. Additionally, PCB2 would elevate the cortical tension in embryo cells at morula and blastocyst stages and further improve blastocyst quality. What’s more, targeted metabolomics shows that PCB2 has a beneficial effect on blastocyst formation by mediating saccharides and amino acids metabolism. CONCLUSIONS: Antioxidant PCB2 exhibits multi-protective roles in response to vitrification stimuli through mitochondria-mediated cortical tension regulation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-022-00742-y. |
format | Online Article Text |
id | pubmed-9380387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93803872022-08-17 Antioxidant procyanidin B2 protects oocytes against cryoinjuries via mitochondria regulated cortical tension Zhuan, Qingrui Li, Jun Du, Xingzhu Zhang, Luyao Meng, Lin Luo, Yuwen Zhou, Dan Liu, Hongyu Wan, Pengcheng Hou, Yunpeng Fu, Xiangwei J Anim Sci Biotechnol Research BACKGROUND: Irreversible cryodamage caused by oocyte vitrification limited its wild application in female fertility preservation. Antioxidants were always used to antagonist the oxidative stress caused by vitrification. However, the comprehensive mechanism underlying the protective role of antioxidants has not been studied. Procyanidin B2 (PCB2) is a potent natural antioxidant and its functions in response to vitrification are still unknown. In this study, the effects of PCB2 on vitrified-thawed oocytes and subsequent embryo development were explored, and the mechanisms underlying the protective role of PCB2 were systematically elucidated. RESULTS: Vitrification induced a marked decline in oocyte quality, while PCB2 could improve oocyte viability and further development after parthenogenetic activation. A subsequent study indicated that PCB2 effectively attenuated vitrification-induced oxidative stress, rescued mitochondrial dysfunction, and improved cell viability. Moreover, PCB2 also acts as a cortical tension regulator apart from strong antioxidant properties. Increased cortical tension caused by PCB2 would maintain normal spindle morphology and promote migration, ensure correct meiosis progression and finally reduce the aneuploidy rate in vitrified oocytes. Further study reveals that ATP biosynthesis plays a crucial role in cortical tension regulation, and PCB2 effectively increased the cortical tension through the electron transfer chain pathway. Additionally, PCB2 would elevate the cortical tension in embryo cells at morula and blastocyst stages and further improve blastocyst quality. What’s more, targeted metabolomics shows that PCB2 has a beneficial effect on blastocyst formation by mediating saccharides and amino acids metabolism. CONCLUSIONS: Antioxidant PCB2 exhibits multi-protective roles in response to vitrification stimuli through mitochondria-mediated cortical tension regulation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-022-00742-y. BioMed Central 2022-08-16 /pmc/articles/PMC9380387/ /pubmed/35971139 http://dx.doi.org/10.1186/s40104-022-00742-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhuan, Qingrui Li, Jun Du, Xingzhu Zhang, Luyao Meng, Lin Luo, Yuwen Zhou, Dan Liu, Hongyu Wan, Pengcheng Hou, Yunpeng Fu, Xiangwei Antioxidant procyanidin B2 protects oocytes against cryoinjuries via mitochondria regulated cortical tension |
title | Antioxidant procyanidin B2 protects oocytes against cryoinjuries via mitochondria regulated cortical tension |
title_full | Antioxidant procyanidin B2 protects oocytes against cryoinjuries via mitochondria regulated cortical tension |
title_fullStr | Antioxidant procyanidin B2 protects oocytes against cryoinjuries via mitochondria regulated cortical tension |
title_full_unstemmed | Antioxidant procyanidin B2 protects oocytes against cryoinjuries via mitochondria regulated cortical tension |
title_short | Antioxidant procyanidin B2 protects oocytes against cryoinjuries via mitochondria regulated cortical tension |
title_sort | antioxidant procyanidin b2 protects oocytes against cryoinjuries via mitochondria regulated cortical tension |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380387/ https://www.ncbi.nlm.nih.gov/pubmed/35971139 http://dx.doi.org/10.1186/s40104-022-00742-y |
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