Time of first polar body extrusion affects the developmental competence of equine oocytes after intracytoplasmic sperm injection.
Abstract: Assisted reproduction techniques (ARTs) have become widespread in the equine breeding industry. In particular, the combination of oocyte recovery from live mares followed by IVM and intracytoplasmic sperm injection (ICSI) has increased markedly among the ARTs used with valuable or low-fertility animals. There is currently no consensus among research groups regarding the optimal oocyte maturation period to produce high-quality embryos. In this study, we report the maturation dynamics of equine oocytes at different time points, from 20 to 40h (Experiment 1). In addition, in Experiment 2, equine ICSI blastocysts were produced from oocytes that exhibited early (up to 24h) or late (28-30h) extrusion of the first polar body (PB). Blastocyst rates and diameter were recorded and embryo quality was assessed by analysing the number of apoptotic cells and Yes-associated protein 1 (YAP1) expression. By 20h of IVM, 42% of oocytes were mature, and the remaining oocytes matured within the next 17h of IVM. Although no differences were found in cell apoptosis or the number of YAP1-positive cells between groups exhibiting early and late PB extrusion, embryos from the early group (Group I) exhibited an improved total cell number and blastocyst rate compared to embryos from the late group (Group II) (18.60% vs 10.17% respectively).
Publication Date: 2019-11-21 PubMed ID: 31747534DOI: 10.1071/RD19248Google Scholar: Lookup
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- Journal Article
Summary
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The research reports on how the timing of the first polar body extrusion during oocyte maturation can impact the developmental competence of equine oocytes after intracytoplasmic sperm injection.
Overview of the Research
- The main objective of this research was to understand the optimal oocyte maturation period for producing high-quality embryos, which is currently a matter of debate among researchers in assisted reproduction techniques (ARTs).
- This research focused on understanding the maturation dynamics of equine oocytes and the role of the timing of the first polar body (PB) extrusion on the subsequent development of embryos.
Research Methodology
- The study was divided into two experiments. The first experiment studied the maturation dynamics of equine oocytes at different time points, ranging from 20 to 40 hours.
- The second experiment studied the effects of early (up to 24 hours) or late (28-30 hours) first polar body extrusion on embryo development.
- The blastocyst rates and diameters were recorded, and embryo quality was evaluated based on the number of apoptotic cells and the expression of Yes-associated protein 1 (YAP1).
Research Findings
- 42% of equine oocytes were found to be mature by 20 hours of in vitro maturation (IVM), and the remaining oocytes matured within the next 17 hours of IVM.
- No difference was found in cell apoptosis or the number of YAP1-positive cells between the groups that had early and late polar body extrusion.
- However, a significant finding was that embryos from the early group (up to 24 hours) showed an improved total cell number and blastocyst rate compared to those from the late group (28-30 hours), indicating a potential advantage in early PB extrusion for embryo development.
Conclusion
- The study concluded that the timing of the first polar body extrusion during oocyte maturation affects the embryo’s developmental competence after intracytoplasmic sperm injection. Early extrusion of the polar body (up to 24 hours) results in better embryo quality compared to late extrusion (28-30 hours).
- These findings can be highly valuable in improving assisted reproduction techniques, particularly in the equine breeding industry where ARTs like IVM and intracytoplasmic sperm injection (ICSI) are widely used.
Cite This Article
APA
Rodríguez MB, Gambini A, Clérico G, Ynsaurralde-Rivolta AE, Briski O, Largel H, Sansinena M, Salamone DF.
(2019).
Time of first polar body extrusion affects the developmental competence of equine oocytes after intracytoplasmic sperm injection.
Reprod Fertil Dev, 31(12), 1805-1811.
https://doi.org/10.1071/RD19248 Publication
Researcher Affiliations
- Laboratorio de Biotecnología Animal, Facultad de Agronomía, Universidad de Buenos Aires, Av. San Martin 4453, Agronomía, C1417DSE CABA, Buenos Aires, Argentina; and Consejo Nacional de Investigaciones Científicas y Técnicas, (CONICET) Godoy Cruz 2290, C1425FQB CABA, Argentina.
- Laboratorio de Biotecnología Animal, Facultad de Agronomía, Universidad de Buenos Aires, Av. San Martin 4453, Agronomía, C1417DSE CABA, Buenos Aires, Argentina; and Consejo Nacional de Investigaciones Científicas y Técnicas, (CONICET) Godoy Cruz 2290, C1425FQB CABA, Argentina.
- Consejo Nacional de Investigaciones Científicas y Técnicas, (CONICET) Godoy Cruz 2290, C1425FQB CABA, Argentina; and Laboratorio de Biotecnología y Reproducción Animal, Facultad de Ingeniería y Ciencias Agrarias, Pontificia Universidad Católica Argentina, Av. Alicia Moreau de Justo 1300, CABA, Buenos Aires, Argentina.
- Instituto Nacional de Tecnología Agropecuaria (INTA), Juan Pujol al Este s/n, 3470 Mercedes, Corrientes, Argentina.
- Laboratorio de Biotecnología Animal, Facultad de Agronomía, Universidad de Buenos Aires, Av. San Martin 4453, Agronomía, C1417DSE CABA, Buenos Aires, Argentina; and Consejo Nacional de Investigaciones Científicas y Técnicas, (CONICET) Godoy Cruz 2290, C1425FQB CABA, Argentina.
- Private practice at El palenque Embriones equine embryo transfer center, Est, Acceso a Lucas Monteverde, B6660 Veinticinco de Mayo, Provincia de Buenos Aires, Argentina.
- Consejo Nacional de Investigaciones Científicas y Técnicas, (CONICET) Godoy Cruz 2290, C1425FQB CABA, Argentina; and Laboratorio de Biotecnología y Reproducción Animal, Facultad de Ingeniería y Ciencias Agrarias, Pontificia Universidad Católica Argentina, Av. Alicia Moreau de Justo 1300, CABA, Buenos Aires, Argentina.
- Laboratorio de Biotecnología Animal, Facultad de Agronomía, Universidad de Buenos Aires, Av. San Martin 4453, Agronomía, C1417DSE CABA, Buenos Aires, Argentina; and Consejo Nacional de Investigaciones Científicas y Técnicas, (CONICET) Godoy Cruz 2290, C1425FQB CABA, Argentina; and Corresponding author. Email: salamone@agro.uba.ar.
MeSH Terms
- Animals
- Blastocyst / cytology
- Blastocyst / physiology
- Blastocyst / ultrastructure
- Cells, Cultured
- Embryo Culture Techniques / veterinary
- Embryo, Mammalian
- Embryonic Development / physiology
- Female
- Horses / embryology
- In Vitro Oocyte Maturation Techniques / veterinary
- Male
- Oocyte Retrieval / methods
- Oocyte Retrieval / veterinary
- Oogenesis / physiology
- Polar Bodies / physiology
- Sperm Injections, Intracytoplasmic / methods
- Sperm Injections, Intracytoplasmic / veterinary
- Time Factors
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