Mitochondria directly influence fertilisation outcome in the pig
Shahinaz H El Shourbagy1, Emma C Spikings, Mariana Freitas
1The Mitochondrial and Reproductive Genetics Group, The Medical School, The University of Birmingham, Birmingham B15 2TT, UK.
Abstract:
The mitochondrion is explicitly involved in cytoplasmic regulation and is the cell's major generator of ATP. Our aim was to determine whether mitochondria alone could influence fertilisation outcome. In vitro, oocyte competence can be assessed through the presence of glucose-6-phosphate dehydrogenase (G6PD) as indicated by the dye, brilliant cresyl blue (BCB). Using porcine in vitro fertilisation (IVF), we have assessed oocyte maturation, cytoplasmic volume, fertilisation outcome, mitochondrial number as determined by mtDNA copy number, and whether mitochondria are uniformly distributed between blastomeres of each embryo. After staining with BCB, we observed a significant difference in cytoplasmic volume between BCB positive (BCB+) and BCB negative (BCB-) oocytes. There was also a significant difference in mtDNA copy number between fertilised and unfertilised oocytes and unequal mitochondrial segregation between blastomeres during early cleavage stages. Furthermore, we have supplemented BCB- oocytes with mitochondria from maternal relatives and observed a significant difference in fertilisation outcomes following both IVF and intracytoplasmic sperm injection (ICSI) between supplemented, sham-injected and non-treated BCB- oocytes. We have therefore demonstrated a relationship between oocyte maturity, cytoplasmic volume, and fertilisation outcome and mitochondrial content. These data suggest that mitochondrial number is important for fertilisation outcome and embryonic development. Furthermore, a mitochondrial pre-fertilisation threshold may ensure that, as mitochondria are diluted out during post-fertilisation cleavage, there are sufficient copies of mtDNA per blastomere to allow transmission of mtDNA to each cell of the post-implantation embryo after the initiation of mtDNA replication during the early postimplantation stages.
Insights
Mitochondrial number in oocytes significantly impacts fertilization success and embryonic development. Supplementing oocytes with mitochondria improves fertilization outcomes, highlighting their crucial role in early development.
Area of Science:
- Cell Biology
- Reproductive Biology
- Mitochondrial Biology
Background:
- Mitochondria are vital for cellular energy (ATP) and cytoplasmic regulation.
- Oocyte competence, assessed by glucose-6-phosphate dehydrogenase (G6PD) via brilliant cresyl blue (BCB) staining, is linked to cytoplasmic factors.
- The specific role of mitochondria in fertilization outcome requires further elucidation.
Purpose of the Study:
- To investigate if mitochondria alone can influence fertilization outcomes.
- To assess the relationship between oocyte maturity, cytoplasmic volume, mitochondrial content, and fertilization success.
- To determine the importance of mitochondrial number for embryonic development.
Main Methods:
- Porcine oocytes were assessed for maturation (BCB staining), cytoplasmic volume, and mitochondrial content (mtDNA copy number).
- Fertilization outcomes were evaluated after in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI).
- Mitochondria were experimentally supplemented into BCB- oocytes to assess functional impact.
Main Results:
- Significant differences in cytoplasmic volume were observed between BCB+ and BCB- oocytes.
- Fertilized oocytes showed higher mtDNA copy numbers than unfertilized ones.
- Supplementation of mitochondria into BCB- oocytes significantly improved fertilization outcomes in both IVF and ICSI.
- Unequal mitochondrial distribution was noted between blastomeres during early embryonic cleavage.
Conclusions:
- Oocyte maturity, cytoplasmic volume, and mitochondrial content are interconnected and influence fertilization success.
- Mitochondrial number is a critical factor for successful fertilization and subsequent embryonic development.
- A sufficient pre-fertilization mitochondrial threshold is essential for maintaining mtDNA integrity during early embryonic cell divisions.
Related Concept Videos
Animal Mitochondrial Genetics
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