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Lack of calcium oscillation causes failure of oocyte activation after intracytoplasmic sperm injection in pigs

In pigs, the efficiency of embryo production after intracytoplasmic sperm injection (ICSI) is still low because of frequent failure of normal fertilization, which involves formation of two polar bodies and two pronuclei. To clarify the reasons for this, we hypothesized that ICSI does not properly tr...

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Detalles Bibliográficos
Autores principales: NAKAI, Michiko, ITO, Junya, SUZUKI, Shun-ichi, FUCHIMOTO, Dai-ichiro, SEMBON, Shoichiro, SUZUKI, Misae, NOGUCHI, Junko, KANEKO, Hiroyuki, ONISHI, Akira, KASHIWAZAKI, Naomi, KIKUCHI, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Society for Reproduction and Development 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5177980/
https://www.ncbi.nlm.nih.gov/pubmed/27725347
http://dx.doi.org/10.1262/jrd.2016-113
Descripción
Sumario:In pigs, the efficiency of embryo production after intracytoplasmic sperm injection (ICSI) is still low because of frequent failure of normal fertilization, which involves formation of two polar bodies and two pronuclei. To clarify the reasons for this, we hypothesized that ICSI does not properly trigger sperm-induced fertilization events, especially intracellular Ca(2+) signaling, also known as Ca(2+) oscillation. We also suspected that the use of in vitro-matured oocytes might negatively affect fertilization events and embryonic development of sperm-injected oocytes. Therefore, we compared the patterns of Ca(2+) oscillation, the efficiency of oocyte activation and normal fertilization, and embryo development to the blastocyst stage among in vivo- or in vitro-matured oocytes after ICSI or in vitro fertilization (IVF). Unexpectedly, we found that the pattern of Ca(2+) oscillation, such as the frequency and amplitude of Ca(2+) rises, in oocytes after ICSI was similar to that in oocytes after IVF, irrespective of the oocyte source. However, half of the oocytes failed to become activated after ICSI and showed no Ca(2+) oscillation. Moreover, the embryonic development of normal fertilized oocytes was reduced when in vitro-matured oocytes were used, irrespective of the fertilization method employed. These findings suggest that low embryo production efficiency after ICSI is attributable mainly to poor developmental ability of in vitro-matured oocytes and a lack of Ca(2+) oscillation, rather than the pattern of oscillation.