卵泡液细胞外囊泡支持牛卵母细胞的能量代谢,改善囊胚发育和质量†。

IF 3.1 2区 生物学 Q2 REPRODUCTIVE BIOLOGY
Paulina Lipinska, Katrien Smits, Ann Van Soom, Krishna Chaitanya Pavani, Ewelina Warzych
{"title":"卵泡液细胞外囊泡支持牛卵母细胞的能量代谢,改善囊胚发育和质量†。","authors":"Paulina Lipinska, Katrien Smits, Ann Van Soom, Krishna Chaitanya Pavani, Ewelina Warzych","doi":"10.1093/biolre/ioaf096","DOIUrl":null,"url":null,"abstract":"<p><p>Extracellular vesicles (EVs), from follicular fluid seem to play a significant role in communication within ovarian follicles in several species. The present study aimed to examine the supporting effect of follicular fluid derived small EVs (FF-sEVs) during in vitro maturation (IVM) of bovine cumulus-oocyte complexes (COCs) under conditions of disturbed energy metabolism. Bovine COCs were matured in vitro with inhibitors targeting lipid metabolism (etomoxir) or glucose metabolism (iodoacetate combined with dehydroepiandrosterone), in the presence or absence of FF-sEVs. Following maturation, oocytes and cumulus cells were analyzed by real-time qPCR and stained to visualize lipid droplets. The uptake of FF-sEVs was visualised by fluorescent labelling. In vitro fertilization and embryo culture were followed by mass spectrometry analysis of hatched blastocysts. We demonstrate for the first time that FF-sEVs are transported from the medium into the oocytes, via the cumulus cells and through transzonal projections (TZPs) into the perivitelline space and ooplasm. Cumulus cells under metabolic stress conditions exhibit an increased FF-sEVs uptake from the maturation medium. FF-sEVs supplementation during metabolic stress conditions enhances the MII rate in oocytes and positively affects subsequent embryo development and quality revealed by altered metabolic activity. Lipid droplet parameters and gene expression in cumulus cells and oocytes are affected by FF-sEVs supplementation, which is more pronounced in cumulus cells. Our findings show that FF-sEVs supplementation during IVM under metabolic stress conditions significantly affects COCs, with a positive effect on further blastocyst quality. We provide novel insights into the role of FF-sEVs in oocyte maturation and blastocyst development.</p>","PeriodicalId":8965,"journal":{"name":"Biology of Reproduction","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Follicular fluid extracellular vesicles support energy metabolism of bovine oocytes, improving blastocyst development and quality†.\",\"authors\":\"Paulina Lipinska, Katrien Smits, Ann Van Soom, Krishna Chaitanya Pavani, Ewelina Warzych\",\"doi\":\"10.1093/biolre/ioaf096\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Extracellular vesicles (EVs), from follicular fluid seem to play a significant role in communication within ovarian follicles in several species. The present study aimed to examine the supporting effect of follicular fluid derived small EVs (FF-sEVs) during in vitro maturation (IVM) of bovine cumulus-oocyte complexes (COCs) under conditions of disturbed energy metabolism. Bovine COCs were matured in vitro with inhibitors targeting lipid metabolism (etomoxir) or glucose metabolism (iodoacetate combined with dehydroepiandrosterone), in the presence or absence of FF-sEVs. Following maturation, oocytes and cumulus cells were analyzed by real-time qPCR and stained to visualize lipid droplets. The uptake of FF-sEVs was visualised by fluorescent labelling. In vitro fertilization and embryo culture were followed by mass spectrometry analysis of hatched blastocysts. We demonstrate for the first time that FF-sEVs are transported from the medium into the oocytes, via the cumulus cells and through transzonal projections (TZPs) into the perivitelline space and ooplasm. Cumulus cells under metabolic stress conditions exhibit an increased FF-sEVs uptake from the maturation medium. FF-sEVs supplementation during metabolic stress conditions enhances the MII rate in oocytes and positively affects subsequent embryo development and quality revealed by altered metabolic activity. Lipid droplet parameters and gene expression in cumulus cells and oocytes are affected by FF-sEVs supplementation, which is more pronounced in cumulus cells. Our findings show that FF-sEVs supplementation during IVM under metabolic stress conditions significantly affects COCs, with a positive effect on further blastocyst quality. We provide novel insights into the role of FF-sEVs in oocyte maturation and blastocyst development.</p>\",\"PeriodicalId\":8965,\"journal\":{\"name\":\"Biology of Reproduction\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biology of Reproduction\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/biolre/ioaf096\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"REPRODUCTIVE BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biology of Reproduction","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/biolre/ioaf096","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"REPRODUCTIVE BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

来自卵泡液的细胞外囊泡(EVs)似乎在几种物种的卵巢卵泡内的通信中起着重要作用。本研究旨在探讨在能量代谢紊乱的条件下,卵泡液衍生的小ev (ff - sev)对牛卵母细胞复合物(COCs)体外成熟(IVM)的支持作用。牛COCs在体外与针对脂代谢(依托莫西)或葡萄糖代谢(碘乙酸酯联合脱氢表雄酮)的抑制剂一起成熟,无论是否存在ff - sev。成熟后,用实时荧光定量pcr分析卵母细胞和卵丘细胞,并染色观察脂滴。通过荧光标记可视化ff - sev的摄取。体外受精和胚胎培养后,对孵化的囊胚进行质谱分析。我们首次证明了ff - sev可以通过积云细胞和跨区投射(TZPs)从培养基转运到卵母细胞和卵周空间和卵浆。代谢应激条件下的积云细胞从成熟培养基中摄取的ff - sev增加。在代谢应激条件下补充FF-sEVs可以提高卵母细胞的MII率,并通过改变代谢活性对随后的胚胎发育和质量产生积极影响。补充FF-sEVs对积云细胞和卵母细胞的脂滴参数和基因表达均有影响,且在积云细胞中更为明显。我们的研究结果表明,代谢应激条件下IVM期间补充ff - sev显著影响COCs,并对囊胚质量产生积极影响。我们对ff - sev在卵母细胞成熟和囊胚发育中的作用提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Follicular fluid extracellular vesicles support energy metabolism of bovine oocytes, improving blastocyst development and quality†.

Extracellular vesicles (EVs), from follicular fluid seem to play a significant role in communication within ovarian follicles in several species. The present study aimed to examine the supporting effect of follicular fluid derived small EVs (FF-sEVs) during in vitro maturation (IVM) of bovine cumulus-oocyte complexes (COCs) under conditions of disturbed energy metabolism. Bovine COCs were matured in vitro with inhibitors targeting lipid metabolism (etomoxir) or glucose metabolism (iodoacetate combined with dehydroepiandrosterone), in the presence or absence of FF-sEVs. Following maturation, oocytes and cumulus cells were analyzed by real-time qPCR and stained to visualize lipid droplets. The uptake of FF-sEVs was visualised by fluorescent labelling. In vitro fertilization and embryo culture were followed by mass spectrometry analysis of hatched blastocysts. We demonstrate for the first time that FF-sEVs are transported from the medium into the oocytes, via the cumulus cells and through transzonal projections (TZPs) into the perivitelline space and ooplasm. Cumulus cells under metabolic stress conditions exhibit an increased FF-sEVs uptake from the maturation medium. FF-sEVs supplementation during metabolic stress conditions enhances the MII rate in oocytes and positively affects subsequent embryo development and quality revealed by altered metabolic activity. Lipid droplet parameters and gene expression in cumulus cells and oocytes are affected by FF-sEVs supplementation, which is more pronounced in cumulus cells. Our findings show that FF-sEVs supplementation during IVM under metabolic stress conditions significantly affects COCs, with a positive effect on further blastocyst quality. We provide novel insights into the role of FF-sEVs in oocyte maturation and blastocyst development.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Biology of Reproduction
Biology of Reproduction 生物-生殖生物学
CiteScore
6.30
自引率
5.60%
发文量
214
审稿时长
1 months
期刊介绍: Biology of Reproduction (BOR) is the official journal of the Society for the Study of Reproduction and publishes original research on a broad range of topics in the field of reproductive biology, as well as reviews on topics of current importance or controversy. BOR is consistently one of the most highly cited journals publishing original research in the field of reproductive biology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信