Masroor Sagheer, Daniel Carballo, Tatiane S Maia, Peter J Hansen
{"title":"Consequences of varying methionine concentrations on development of the bovine embryo in vitro†.","authors":"Masroor Sagheer, Daniel Carballo, Tatiane S Maia, Peter J Hansen","doi":"10.1093/biolre/ioaf111","DOIUrl":null,"url":null,"abstract":"<p><p>Methionine is an essential amino acid that influences key cellular processes. This study examined how methionine concentrations representing deficiency (0 μM), estimated uterine concentration in cows (31 μM), and a supra-physiological concentration (i.e. rumen-protected methionine; 57 μM) affect bovine preimplantation embryo development. When compared to 31 and 57 μM methionine, methionine deficiency (0 μM) reduced the percentage of zygotes developing into blastocysts by day 7.5 and the proportion of blastocysts that hatched at day 7.5, 8.5, and 9.5. Blastocysts produced without methionine developed slowly, had fewer total, CDX2+(trophectoderm), and SOX2+(inner cell mass) cells, and exhibited higher apoptosis and lipid content. Increasing methionine from 31 to 57 μM did not improve blastocyst development or hatching but increased CDX2+cells number and reduced apoptosis and lipid content. Methionine concentration had no effect on survival to vitrification. In conclusion, the absence of methionine reduces the competence of zygotes to become a blastocyst and has detrimental effects on the properties of those blastocysts. A higher methionine concentration increases trophectoderm cell number, reduces apoptosis, and lowers lipid accumulation. These findings suggest that nutritional strategies to increase methionine availability during the periconceptional period may enhance blastocyst competence for continued development.</p>","PeriodicalId":8965,"journal":{"name":"Biology of Reproduction","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-05-19","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/ioaf111","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
Abstract
Methionine is an essential amino acid that influences key cellular processes. This study examined how methionine concentrations representing deficiency (0 μM), estimated uterine concentration in cows (31 μM), and a supra-physiological concentration (i.e. rumen-protected methionine; 57 μM) affect bovine preimplantation embryo development. When compared to 31 and 57 μM methionine, methionine deficiency (0 μM) reduced the percentage of zygotes developing into blastocysts by day 7.5 and the proportion of blastocysts that hatched at day 7.5, 8.5, and 9.5. Blastocysts produced without methionine developed slowly, had fewer total, CDX2+(trophectoderm), and SOX2+(inner cell mass) cells, and exhibited higher apoptosis and lipid content. Increasing methionine from 31 to 57 μM did not improve blastocyst development or hatching but increased CDX2+cells number and reduced apoptosis and lipid content. Methionine concentration had no effect on survival to vitrification. In conclusion, the absence of methionine reduces the competence of zygotes to become a blastocyst and has detrimental effects on the properties of those blastocysts. A higher methionine concentration increases trophectoderm cell number, reduces apoptosis, and lowers lipid accumulation. These findings suggest that nutritional strategies to increase methionine availability during the periconceptional period may enhance blastocyst competence for continued development.
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.