Oocyte activation with phospholipase Cζ mRNA induces repetitive intracellular Ca 2+ rises and improves the quality of pig embryos after intracytoplasmic sperm injection

• Published in: The Journal of reproduction and development Vol. 70; no. 4; p. 229
• Main Authors: Nakai, Michiko, Suzuki, Shun-Ichi, Fuchimoto, Dai-Ichiro, Sembon, Shoichiro, Kikuchi, Kazuhiro
• Format: Journal Article
• Language: English
• Published: Japan 07.08.2024
• Subjects: Animals; Blastocyst - metabolism; Calcium - metabolism; Calcium Signaling; Embryonic Development; Female; Fertilization; Fertilization in Vitro - veterinary; Male; Oocytes - metabolism; Phosphoinositide Phospholipase C - genetics; Phosphoinositide Phospholipase C - metabolism; RNA, Messenger - metabolism; Sperm Injections, Intracytoplasmic; Spermatozoa - metabolism; Swine; Oocyte activation; Phospholipase Cζ; Intracytoplasmic sperm injection (ICSI); Pig
• ISSN: 1348-4400
• DOI: 10.1262/jrd.2023-105

For the intracytoplasmic sperm injection (ICSI) procedure in pigs, an electrical pulse (EP) has been used as an effective method for oocyte stimulation, but unlike sperm, EP is unable to induce Ca oscillations. In this study, we investigated the effects of generating artificial Ca oscillations with phospholipase Cζ (PLCζ) mRNA, a candidate sperm factor, on fertilization, embryonic development, and gene expression after ICSI. Firstly, the concentration of PLCζ mRNA of a fixed volume (1.0 pl) that would induce a pattern of Ca rise similar to that of in vitro fertilized (IVF) sperm was examined and determined to be 300 ng/μl. Secondly, the effects of oocyte stimulation methods on fertilization and embryonic development were investigated. ICSI-oocytes were activated by EP (EP group) or by PLCζ mRNA (PLCζ group). Furthermore, IVF-oocytes (IVF group) and ICSI-oocytes with and without an injection of buffer (buffer and untreated groups, respectively) were used as controls. It was found that the rates of normal fertilization in the PLCζ and EP groups were significantly higher than those in the buffer and untreated groups. The blastocyst formation rates did not differ among the groups. The embryo quality in the EP group was inferior to those in the PLCζ and IVF groups. Additionally, the expression level of a proapoptosis-related gene (Caspase-3) in the EP group was significantly higher than those in the PLCζ and IVF groups. Our data suggest that oocyte activation by PLCζ mRNA has the effect of improving embryo quality.