{"title":"Multi-omics profiling uncovers metabolic regulation in cumulus cells during oocyte maturation","authors":"Yassin Kassim , Hao Sheng , Haibin Zhong , Mostafa Elashry , Omaima Mohamed Kandil , Esraa Aly Ismail , Kun Zhang","doi":"10.1016/j.anireprosci.2026.108121","DOIUrl":null,"url":null,"abstract":"<div><div>Bidirectional signalling between the oocyte and surrounding cumulus cells is essential for coordinating follicular development and acquiring oocyte competence. The metabolic networks governing bovine cumulus cell function, however, remain poorly characterized. To address this gap, we performed integrated metabolomic and proteomic analyses of cumulus cells isolated from cumulus-oocyte complexes at two critical maturation stages: (1) meiotically arrested germinal vesicle stage (0 h) and (2) metaphase II stage (24 h). This temporal profiling reveals dynamic metabolic reprogramming events supporting oocyte maturation. In particular, we found the active use of glucose metabolism via glycolysis and the pentose phosphate pathway, rather than the citric cycle, suppression in fatty acid β-oxidation, and active tryptophan and polyamine biosynthesis. Meanwhile, the surrounding cumulus cells showed a steady rise in steroid hormone production and one-carbon metabolism in tandem with the development of the oocyte. In sum, the data provide a comprehensive metabolic atlas of cumulus cell differentiation and give prospective indicators for enhancing and predicting oocyte quality.</div></div>","PeriodicalId":7880,"journal":{"name":"Animal Reproduction Science","volume":"288 ","pages":"Article 108121"},"PeriodicalIF":3.3000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animal Reproduction Science","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378432026000242","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/3 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Bidirectional signalling between the oocyte and surrounding cumulus cells is essential for coordinating follicular development and acquiring oocyte competence. The metabolic networks governing bovine cumulus cell function, however, remain poorly characterized. To address this gap, we performed integrated metabolomic and proteomic analyses of cumulus cells isolated from cumulus-oocyte complexes at two critical maturation stages: (1) meiotically arrested germinal vesicle stage (0 h) and (2) metaphase II stage (24 h). This temporal profiling reveals dynamic metabolic reprogramming events supporting oocyte maturation. In particular, we found the active use of glucose metabolism via glycolysis and the pentose phosphate pathway, rather than the citric cycle, suppression in fatty acid β-oxidation, and active tryptophan and polyamine biosynthesis. Meanwhile, the surrounding cumulus cells showed a steady rise in steroid hormone production and one-carbon metabolism in tandem with the development of the oocyte. In sum, the data provide a comprehensive metabolic atlas of cumulus cell differentiation and give prospective indicators for enhancing and predicting oocyte quality.
期刊介绍:
Animal Reproduction Science publishes results from studies relating to reproduction and fertility in animals. This includes both fundamental research and applied studies, including management practices that increase our understanding of the biology and manipulation of reproduction. Manuscripts should go into depth in the mechanisms involved in the research reported, rather than a give a mere description of findings. The focus is on animals that are useful to humans including food- and fibre-producing; companion/recreational; captive; and endangered species including zoo animals, but excluding laboratory animals unless the results of the study provide new information that impacts the basic understanding of the biology or manipulation of reproduction.
The journal''s scope includes the study of reproductive physiology and endocrinology, reproductive cycles, natural and artificial control of reproduction, preservation and use of gametes and embryos, pregnancy and parturition, infertility and sterility, diagnostic and therapeutic techniques.
The Editorial Board of Animal Reproduction Science has decided not to publish papers in which there is an exclusive examination of the in vitro development of oocytes and embryos; however, there will be consideration of papers that include in vitro studies where the source of the oocytes and/or development of the embryos beyond the blastocyst stage is part of the experimental design.