» Articles » PMID: 32393337

Prostaglandin E Affects in Vitro Maturation of Bovine Oocytes

Overview
Publisher Biomed Central
Date 2020 May 13
PMID 32393337
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

The role of prostaglandin E (PGE) in the successful resumption of oocyte meiosis and cumulus expansion has been well-documented. However, there remains very little information available on the influence of PGE on other processes that occur during oocyte maturation. In this study, we supplemented a maturation medium with PGE and monitored oocyte quality markers, glucose metabolism, mitochondrial status, oxidative stress, and apoptosis in the cumulus-oocyte complexes (COCs), using a well-established in vitro model of embryo production in cattle. We found that this increased availability of PGE during maturation led to an increase in the expression of genes associated with oocyte competence and improved the quality of blastocysts produced. Prostaglandin E also appeared to stimulate glucose uptake and lactate production in the COCs, both influencing the expression of enzymes involved in glycolysis and the hexosamine biosynthetic pathway. We found that PGE reduced intracellular reactive oxygen species levels, and simultaneously increased glutathione concentration and stimulated antioxidant gene expression in the oocyte. These results indicate that PGE has an important role in the protection of oocytes against oxidative stress. Mitochondrial membrane potential was also improved in PGE-treated oocytes, and there was a reduction in the occurrence of apoptosis in the COCs. Promotion of an anti-apoptotic balance in transcription of genes involved in apoptosis was present in both oocytes and the cumulus cells. In summary, PGE could represent a novel autocrine/paracrine player in the mechanisms that can facilitate successful oocyte maturation and oocyte survival in the cow.

Citing Articles

Metabolomics-Driven Insights into Biomarkers for Poor Ovarian Response: A Narrative Review.

Potiris A, Stavros S, Alyfanti E, Machairiotis N, Drakaki E, Zikopoulos A Biomedicines. 2025; 13(1).

PMID: 39857797 PMC: 11762483. DOI: 10.3390/biomedicines13010214.


Multi-Omics Reveals the Role of Arachidonic Acid Metabolism in the Gut-Follicle Axis for the Antral Follicular Development of Holstein Cows.

Guo Y, Wang S, Wu X, Zhao R, Chang S, Ma C Int J Mol Sci. 2024; 25(17).

PMID: 39273467 PMC: 11395146. DOI: 10.3390/ijms25179521.


The Simulated Physiological Oocyte Maturation (SPOM) System Enhances Cytoplasmic Maturation and Oocyte Competence in Cattle.

Navarro M, Fanti T, Ortega N, Waremkraut M, Guaimas F, Mutto A Animals (Basel). 2024; 14(13).

PMID: 38998004 PMC: 11240716. DOI: 10.3390/ani14131893.


Unravelling the role of HAS2, GREM1, and PTGS2 gene expression in cumulus cells: implications for human oocyte development competency - a systematic review and integrated bioinformatic analysis.

Faizal A, Elias M, Mat Jin N, Abu M, Syafruddin S, Zainuddin A Front Endocrinol (Lausanne). 2024; 15:1274376.

PMID: 38524634 PMC: 10957552. DOI: 10.3389/fendo.2024.1274376.


Integrated metabolomics and transcriptomics to reveal biomarkers and mitochondrial metabolic dysregulation of premature ovarian insufficiency.

Yu Z, Peng W, Li F, Fu X, Wang J, Ding H Front Endocrinol (Lausanne). 2024; 14:1280248.

PMID: 38179298 PMC: 10764474. DOI: 10.3389/fendo.2023.1280248.


References
1.
Furnus C, de Matos D, Moses D . Cumulus expansion during in vitro maturation of bovine oocytes: relationship with intracellular glutathione level and its role on subsequent embryo development. Mol Reprod Dev. 1998; 51(1):76-83. DOI: 10.1002/(SICI)1098-2795(199809)51:1<76::AID-MRD9>3.0.CO;2-T. View

2.
Kowaltowski A, Vercesi A . Mitochondrial damage induced by conditions of oxidative stress. Free Radic Biol Med. 1999; 26(3-4):463-71. DOI: 10.1016/s0891-5849(98)00216-0. View

3.
Sutton M, Gilchrist R, Thompson J . Effects of in-vivo and in-vitro environments on the metabolism of the cumulus-oocyte complex and its influence on oocyte developmental capacity. Hum Reprod Update. 2003; 9(1):35-48. DOI: 10.1093/humupd/dmg009. View

4.
Sutton-McDowall M, Gilchrist R, Thompson J . The pivotal role of glucose metabolism in determining oocyte developmental competence. Reproduction. 2010; 139(4):685-95. DOI: 10.1530/REP-09-0345. View

5.
Liu Z, Fan H, Wang Y, Richards J . Targeted disruption of Mapk14 (p38MAPKalpha) in granulosa cells and cumulus cells causes cell-specific changes in gene expression profiles that rescue COC expansion and maintain fertility. Mol Endocrinol. 2010; 24(9):1794-804. PMC: 2940481. DOI: 10.1210/me.2010-0086. View