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Updated: Jan 31, 2026

Manipulation and In Vitro Maturation of Xenopus laevis Oocytes, Followed by Intracytoplasmic Sperm Injection, to Study Embryonic Development
Published on: February 9, 2015
The Unique Mechanisms of Cellular Proliferation, Migration and Apoptosis are Regulated through Oocyte Maturational
Błażej Chermuła1, Maciej Brązert2, Michal Jeseta3
1Division of Infertility and Reproductive Endocrinology, Department of Gynecology, Obstetrics and Gynecological Oncology, Poznan University of Medical Sciences, 60-535 Poznań, Poland. blazej.chermula@wp.pl.
Abstract:
The growth and development of oocyte affect the functional activities of the surrounding somatic cells. These cells are regulated by various types of hormones, proteins, metabolites, and regulatory molecules through gap communication, ultimately leading to the development and maturation of oocytes. The close association between somatic cells and oocytes, which together form the cumulus-oocyte complexes (COCs), and their bi-directional communication are crucial for the acquisition of developmental competences by the oocyte. In this study, oocytes were extracted from the ovaries obtained from crossbred landrace gilts and subjected to in vitro maturation. RNA isolated from those oocytes was used for the subsequent microarray analysis. The data obtained shows, for the first time, variable levels of gene expression (fold changes higher than |2| and adjusted p-value < 0.05) belonging to four ontological groups: regulation of cell proliferation (GO:0042127), regulation of cell migration (GO:0030334), and regulation of programmed cell death (GO:0043067) that can be used together as proliferation, migration or apoptosis markers. We have identified several genes of porcine oocytes (ID2, VEGFA, BTG2, ESR1, CCND2, EDNRA, ANGPTL4, TGFBR3, GJA1, LAMA2, KIT, TPM1, VCP, GRID2, MEF2C, RPS3A, PLD1, BTG3, CD47, MITF), whose expression after in vitro maturation (IVM) is downregulated with different degrees. Our results may be helpful in further elucidating the molecular basis and functional significance of a number of gene markers associated with the processes of migration, proliferation and angiogenesis occurring in COCs.
Insights
Somatic and oocyte cells communicate to regulate development. This study identified porcine oocyte genes involved in cell proliferation, migration, and apoptosis, crucial for maturation and developmental competence.
Area of Science:
- Reproductive Biology
- Molecular Genetics
- Cell Biology
Background:
- Oocyte development relies on communication with surrounding somatic cells within cumulus-oocyte complexes (COCs).
- Bidirectional signaling between oocytes and somatic cells is vital for acquiring developmental competence.
- Hormones, proteins, and metabolites regulate these interactions via gap junctions.
Purpose of the Study:
- To investigate gene expression changes in porcine oocytes during in vitro maturation (IVM).
- To identify novel gene markers associated with proliferation, migration, and apoptosis in COCs.
- To elucidate the molecular basis of COC development and oocyte maturation.
Main Methods:
- Ovaries from crossbred landrace gilts were used to extract oocytes.
- Oocytes underwent in vitro maturation (IVM).
- RNA sequencing and microarray analysis were performed on isolated oocyte RNA.
Main Results:
- Significant differential gene expression (|fold change| > 2, adjusted p-value < 0.05) was observed in four ontological groups: cell proliferation, cell migration, and programmed cell death.
- Several porcine oocyte genes, including ID2, VEGFA, BTG2, ESR1, CCND2, EDNRA, ANGPTL4, TGFBR3, GJA1, LAMA2, KIT, TPM1, VCP, GRID2, MEF2C, RPS3A, PLD1, BTG3, CD47, and MITF, showed downregulation after IVM.
- These identified genes provide potential markers for proliferation, migration, and apoptosis processes in COCs.
Conclusions:
- Gene expression profiling during IVM reveals key regulators of COC development.
- Downregulated genes identified in this study are potential markers for oocyte maturation and developmental competence.
- Understanding these gene markers can advance research into reproductive technologies and fertility.
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