Koo Deog-Bon, Kim Yong-Jun, Yu Iljung, Kim Ha-Na, Lee Kyung-Kwang, Han Yong-Mahn
Laboratory of Development and Differentiation, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Yuseong, Daejeon.
Anim Reprod Sci. 2005 Nov;90(1-2):101-10. doi: 10.1016/j.anireprosci.2005.01.005.
The present study was to investigate the effects of in vitro fertilization conditions on in vitro development and structural integrity of pig embryos. Porcine oocytes matured in vitro were co-incubated with four different spermatozoa concentrations (0.6 x 10(5), 1.2 x 10(5), 2.5 x 10(5) and 5 x 10(5) cells/ml) for 6 h, and at a spermatozoa concentration (1.2 x 10(5) cells/ml) for 2, 4 and 6 h, respectively. Spermatozoa penetration and blastocyst formation were observed at 10 and 144 h post insemination, respectively. The allocation of a blastocyst to inner cell mass (ICM) and trophectoderm (TE) cells was determined by using a differential staining method. Polyspermy frequency increased with increasing spermatozoa concentrations. The spermatozoa-oocyte co-incubation period of 2 h provided for decreased in vitro development rate than 4 and 6 h groups (P < 0.05), although no difference was detected in polyspermy frequency between spermatozoa-oocyte co-incubation periods. Interestingly, blastocysts derived from the groups with greater spermatozoa concentrations (2.5 x 10(5) and 5 x 10(5) cells/ml) had significantly fewer ICM cell nuclei as compared with those groups with lesser spermatozoa concentrations (0.6 x 10(5) and 1.2 x 10(5) cells/ml). There was no difference in the structural integrity of blastocysts among the co-incubation periods. Blastocysts derived from respective experiments were individually classified into three groups (I: <20%; II: 20-40% and III: >40%) based on the ratio of ICM to total cells. Proportion of blastocysts in Group II, with a presumptive normal range of structural integrity, was slightly decreased in the groups with greater spermatozoa concentrations (2.5 x 10(5) and 5 x 10(5) cells/ml). The results indicate that the spermatozoa concentration during in vitro fertilization may be important for developmental competence and quality of pig embryos.
本研究旨在探讨体外受精条件对猪胚胎体外发育及结构完整性的影响。将体外成熟的猪卵母细胞与四种不同精子浓度(0.6×10⁵、1.2×10⁵、2.5×10⁵和5×10⁵个细胞/毫升)共同孵育6小时,以及分别在精子浓度为1.2×10⁵个细胞/毫升的条件下孵育2、4和6小时。分别在授精后10小时和144小时观察精子穿透和囊胚形成情况。采用差异染色法确定囊胚内细胞团(ICM)和滋养外胚层(TE)细胞的分配。多精受精频率随精子浓度增加而升高。精子 - 卵母细胞共同孵育2小时组的体外发育率低于4小时和6小时组(P < 0.05),尽管在不同精子 - 卵母细胞共同孵育时间段之间未检测到多精受精频率的差异。有趣的是,与精子浓度较低组(0.6×10⁵和1.2×10⁵个细胞/毫升)相比,精子浓度较高组(2.5×10⁵和5×10⁵个细胞/毫升)来源的囊胚ICM细胞核显著减少。共同孵育时间段之间囊胚的结构完整性无差异。根据ICM与总细胞的比例,将各实验来源的囊胚分别分为三组(I:<20%;II:20 - 40%和III:>40%)。结构完整性推测在正常范围内的II组囊胚比例,在精子浓度较高组(2.5×10⁵和5×10⁵个细胞/毫升)中略有下降。结果表明,体外受精期间的精子浓度可能对猪胚胎的发育能力和质量很重要。