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Increased apoptosis in late-developing in vitro fertilized bovine blastocysts decreases successful pregnancy

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dc.contributor.authorKim Tae-Gyun-
dc.contributor.authorChoe Yong-Ho-
dc.contributor.authorKim Sung-Ho-
dc.contributor.authorLee Sang-Yup-
dc.contributor.authorJang Min-
dc.contributor.authorYun Sung-Ho-
dc.contributor.authorKim Seung-Joon-
dc.contributor.authorLee Sung-Lim-
dc.contributor.authorLee Won-Jae-
dc.date.accessioned2025-03-06T09:00:08Z-
dc.date.available2025-03-06T09:00:08Z-
dc.date.issued2025-03-
dc.identifier.issn2765-0189-
dc.identifier.issn2765-0235-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/77319-
dc.description.abstractObjective: Pregnancy in cattle after embryo transfer (ET) is influenced by several factors, including embryo quality. Therefore, preparing high-quality embryos with the greatest developmental potential is essential for achieving a successful pregnancy after ET. Meanwhile, blastocysts produced by <i>in vitro</i> fertilization (IVF) procedure have different developmental speed during <i>in vitro</i> culture (IVC) and they exhibited different competence in the establishment of pregnancy.Methods: This study aimed to identify the comparative features of early-, mid-, and late-developing bovine IVF blastocysts, when they first appeared at Day 7, 8, and 9 during IVC, respectively. In addition, the correlations between their molecular features and pregnancy ability were analyzed.Results: The results showed no difference in the morphological characteristics, including total cell count and diameter, between the Day 7, 8, and 9 blastocysts. However, the pregnancy rate post-ET was significantly different between the groups at 51.7%, 36.7%, and 17.8% for Day 7, 8, and 9 blastocysts, respectively. During early embryo development, late-developing blastocysts demonstrated a reduced cell count in the inner cell mass and decreased expression of the early embryo developmental genes (<i>Oct4</i> and <i>Sox2</i>) compared with the early- and mid-developing blastocysts. In addition, the number of apoptotic cells and apoptosis-related gene expression (increased <i>Bax</i> and decreased <i>Bcl2</i>) gradually elevated from the Day 7 to Day 9 blastocysts. However, there was no difference in mitochondrial activity and mitochondria-relevant gene expression (<i>Tfam</i> and <i>Cox1</i>) between the groups. Correlation analysis identified a significantly negative correlation between the pregnancy rate and the blastocysts’ degree of apoptosis, indicating that the low pregnancy ability of late-developing blastocysts was mainly caused by increased apoptosis.Conclusion: This study’s results may contribute to the field of animal biotechnology by assisting in establishing an improved strategy for bovine ET with IVF embryos.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherASIAN-AUSTRALASIAN ASSOC ANIMAL PRODUCTION SOC-
dc.titleIncreased apoptosis in late-developing in vitro fertilized bovine blastocysts decreases successful pregnancy-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.5713/ab.24.0454-
dc.identifier.scopusid2-s2.0-85219375298-
dc.identifier.wosid001460077600007-
dc.identifier.bibliographicCitationAnimal Bioscience, v.38, no.3, pp 454 - 465-
dc.citation.titleAnimal Bioscience-
dc.citation.volume38-
dc.citation.number3-
dc.citation.startPage454-
dc.citation.endPage465-
dc.type.docTypeArticle-
dc.identifier.kciidART003175175-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaAgriculture-
dc.relation.journalWebOfScienceCategoryAgriculture, Dairy & Animal Science-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusEMBRYO-TRANSFER-
dc.subject.keywordPlusPREIMPLANTATION-
dc.subject.keywordPlusOOCYTES-
dc.subject.keywordPlusCATTLE-
dc.subject.keywordPlusBAX-
dc.subject.keywordAuthorApoptosis-
dc.subject.keywordAuthorBovine Blastocyst-
dc.subject.keywordAuthorEmbryo Developmental Speed-
dc.subject.keywordAuthorEmbryo Transfer-
dc.subject.keywordAuthorHanwoo-
dc.subject.keywordAuthorPregnancy Rate-
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