Reproduction · 2006 · 316 citations · 71 references
Life SciencesBiologyCell BiologyEmbryologyIn Vitro FertilizationReproductive BiologyFertilization AssessmentMitochondrial BioenergeticsMitochondrial FunctionMitochondrial MetabolismOocyte MaturationOogenesisCleavage StagesIntracytoplasmic Sperm Injection FertilizationMitochondrial Assessment In OocytesMitochondrial Dna Copy Number VariationMitochondrial Function In BlastocystsOocyte DevelopmentOocyte Fertilization AssessmentOocyte Maturation Stage
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.
71
Sequence and organization of the human mitochondrial genome
Stephen K. Anderson, Alan T. Bankier, B. G. Barrell et al. · Nature · 1981 · 9.7K citations
Viable offspring derived from fetal and adult mammalian cells
I. Wilmut, Angelika Schnieke, J. McWhir et al. · Nature · 1997 · 4.9K citations
Mitochondrial control of nuclear apoptosis.
Naoufal Zamzami, Santos A. Susín, Philippe Marchetti et al. · The Journal of Experimental Medicine · 1996 · 1.4K citations · Full text