Institute of Animal Science, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Theriogenology. 2011 Mar 15;75(5):826-31. doi: 10.1016/j.theriogenology.2010.10.023. Epub 2010 Dec 8.
The objective was to determine whether enucleated oocytes injected with frozen porcine first polar bodies (pPB1s) could be fertilized and developed into viable embryos in vitro. Metaphase II (MII) oocytes with pPB1s were frozen (vitrified) and stored for 2 mo. The pPB1s were isolated from thawed MII oocytes and injected into enucleated recipient oocytes by micromanipulation. All recipients injected with thawed pPB1s were fertilized by intracytoplasmic sperm injection (ICSI), and the resulting recombinant zygotes were incubated to assess their developmental competence in vitro. Furthermore, double-antibody immunohistochemistry was used to verify that the nucleus of the pPB1 participated in fertilization and supported embryonic development. Porcine embryos (2- to 8-cell stage) were obtained from the recombinants. The average in vitro cleavage rate of 2-, 4-, and 8-cell stage recombinant embryos was 25.3, 17.7, and 9.3% (P < 0.05), respectively. Chromosomes in the labeled pPB1 participated in the formation of the two blastomere nuclei of 2-cell stage embryos derived from recombinant oocytes. In conclusion, nuclear materials of frozen-thawed pPB1 supported oocyte fertilization and subsequent embryonic development, thereby providing a new way to use frozen PB1s for preservation and reproduction of mammals.
目的是确定去核卵母细胞注射冷冻猪第一极体(pPB1)后是否能够受精,并在体外发育成有活力的胚胎。将带有 pPB1 的中期 II(MII)卵母细胞冷冻(玻璃化)并储存 2 个月。将 pPB1 从解冻的 MII 卵母细胞中分离出来,通过显微操作注入去核的受体卵母细胞中。所有注射解冻 pPB1 的受体均通过胞质内精子注射(ICSI)受精,并孵育重组受精卵以评估其体外发育能力。此外,还使用双抗体免疫组织化学来验证 pPB1 的核参与受精并支持胚胎发育。从重组体中获得猪胚胎(2-8 细胞期)。2、4 和 8 细胞期重组胚胎的体外平均分裂率分别为 25.3%、17.7%和 9.3%(P<0.05)。标记的 pPB1 中的染色体参与了源自重组卵母细胞的 2 细胞期胚胎两个卵裂球核的形成。总之,冷冻解冻的 pPB1 的核物质支持卵母细胞受精和随后的胚胎发育,从而为使用冷冻 PB1 保存和繁殖哺乳动物提供了一种新方法。