Matsukawa Kazutsugu, Turco Margherita Yayoi, Scapolo Pier Augusto, Reynolds Lawrence, Ptak Grazyna, Loi Pasqualino
Department of Comparative Biomedical Sciences, University of Teramo, Italy.
Cloning Stem Cells. 2007 Fall;9(3):374-81. doi: 10.1089/clo.2006.0016.
Androgenetic embryos are useful model for investigating the contribution of the paternal genome to embryonic development. Little work has been done with androgenetic embryo production in domestic animals. The aim of this study was the production of diploid androgenetic sheep embryos. In vitro matured sheep oocytes were enucleated and fertilized in vitro; parthenogenetic and normally fertilized embryos were also produced as a control. Fifteen hours after in vitro fertilization (IVF), presumptive zygotes were centrifuged and scored for the number of pronucleus. IVF, parthenogenetic, and androgenetic embryos (haploid, diploid, and triploid) were cultured in SOFaa medium with bovine serum albumin (BSA). The proportion of oocytes with polyspermic fertilization increased linearly with increasing sperm concentration. After IVF, there was no significant difference in early cleavage and morula formation rates between the groups, while there was a significant difference on blastocyst development between IVF, parthenogenetic, and androgenetic embryos, the last ones displaying poor developmental potential (IVF, parthenogenetic, and haploid, diploid, and triploid androgenetic embryos: 43%, 38%, 0%, 2%, and 2%, respectively). In order to boost androgenetic embryonic development, we produced diploid androgenetic embryos through pronuclear transfer. Single pronuclei were aspirated with a bevelled pipette from haploid or diploid embryos and transferred into the perivitelline space of other haploid embryos, and the zygotes were reconstructed by electrofusion. Fusion rates approached 100%. Pronuclear transfer significantly increased blastocyst development (IVF, parthenogenetic, androgenetic: Diploid into Haploid, and Haploid into Haploid: 42%, 42%, 19%, and 3%, respectively); intriguingly, the Haploid + Diploid group showed the highest development to blastocyst stage. The main findings of our study are: (1) sheep androgenetic embryos display poor developmental ability compared with IVF and parthenogenetic embryos; (2) diploid androgenetic embryos produced by pronuclear exchange developed in higher proportion to blastocyst stage, particularly in the Diploid-Haploid group. In conclusion, pronuclear transfer is an effective method to produce sheep androgenetic blastocysts.
孤雄胚胎是研究父本基因组对胚胎发育贡献的有用模型。在家畜中,关于孤雄胚胎生产的研究较少。本研究的目的是生产二倍体孤雄绵羊胚胎。体外成熟的绵羊卵母细胞去核后进行体外受精;同时也生产了孤雌胚胎和正常受精胚胎作为对照。体外受精(IVF)15小时后,对假定的合子进行离心,并统计原核数量。将IVF、孤雌和孤雄胚胎(单倍体、二倍体和三倍体)在添加牛血清白蛋白(BSA)的SOFaa培养基中培养。多精受精的卵母细胞比例随精子浓度增加呈线性上升。IVF后,各组之间的早期卵裂和桑椹胚形成率无显著差异,而IVF、孤雌和孤雄胚胎在囊胚发育方面存在显著差异,孤雄胚胎的发育潜能较差(IVF、孤雌、单倍体、二倍体和三倍体孤雄胚胎的囊胚发育率分别为43%、38%、0%、2%和2%)。为了促进孤雄胚胎发育,我们通过原核移植生产二倍体孤雄胚胎。用斜面吸管从单倍体或二倍体胚胎中吸出单个原核,转移到其他单倍体胚胎的卵周隙中,通过电融合重建合子。融合率接近100%。原核移植显著提高了囊胚发育率(IVF、孤雌、孤雄:二倍体到单倍体,单倍体到单倍体:分别为42%、42%、19%和3%);有趣的是,单倍体+二倍体组的囊胚发育率最高。我们研究的主要发现是:(1)与IVF和孤雌胚胎相比,绵羊孤雄胚胎的发育能力较差;(2)通过原核交换产生的二倍体孤雄胚胎发育到囊胚阶段的比例更高,尤其是在二倍体-单倍体组。总之,原核移植是生产绵羊孤雄囊胚的有效方法。