Author:
Tanga Bereket Molla,Fang Xun,Bang Seonggyu,Seo Chaerim,Kang Heejae,Cha Dabin,Qamar Ahmad Yar,Shim Joohyun,Choi Kimyung,Saadeldin Islam M.,Lee Sanghoon,Cho Jongki
Abstract
AbstractIn vitro maturation of porcine oocytes is characterized by asynchronous cytoplasmic and nuclear maturation, leading to less competent oocytes supporting embryo development. The purpose of this study was to evaluate the combined effect of rolipram and cilostamide as cyclic Adenine monophosphate (cAMP) modulators to find the maximum cAMP levels that temporarily arrest meiosis. We determined the optimal time to maintain functional gap junction communication during pre-in vitro maturation to be four hours. Oocyte competence was evaluated by the level of glutathione, reactive oxygen species, meiotic progression, and gene expression. We evaluated embryonic developmental competence after parthenogenetic activation and somatic cell nuclear transfer. The combined treatment group showed significantly higher glutathione and lower reactive oxygen species levels and a higher maturation rate than the control and single treatment groups. Cleavage and blastocyst formation rates in parthenogenetic activation and somatic cell nuclear transfer embryos were higher in two-phase in vitro maturation than in the other groups. The relative levels of BMP15and GDF9 expression were increased in two-phase in vitro maturation. Somatic cell nuclear transfer blastocysts from two-phase in vitro maturation oocytes showed a lower level of expression of apoptotic genes than the control, indicating better pre-implantation developmental competence. The combination of rolipram and cilostamide resulted in optimal synchrony of cytoplasmic and nuclear maturation in porcine in vitro matured oocytes and there by enhanced the developmental competence of pre-implantation embryos.
Funder
National Research Foundation of Korea
Publisher
Springer Science and Business Media LLC
Reference109 articles.
1. Lai, L. et al. Production of alpha-1,3-galactosyltransferase knockout pigs by nuclear transfer cloning. Science 295(5557), 1089–1092 (2002).
2. Polejaeva, I. A. et al. Cloned pigs produced by nuclear transfer from adult somatic cells. Nature 407(6800), 86–90 (2000).
3. Yin, X. J. et al. Production of cloned pigs from adult somatic cells by chemically assisted removal of maternal chromosomes. Biol. Reprod. 67(2), 442–446 (2002).
4. Boquest, A. C. et al. Production of cloned pigs from cultured fetal fibroblast cells. Biol. Reprod. 66(5), 1283–1287 (2002).
5. Cho, J. et al. Improved efficiencies in the generation of multigene-modified pigs by recloning and using sows as the recipient. Zygote 30, 1–8 (2021).
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献