Laboratory of Veterinary Embryology and Biotechnology, College of Veterinary Medicine, Chungbuk National University, Cheongju, Republic of Korea.
Theriogenology. 2012 Apr 1;77(6):1186-97. doi: 10.1016/j.theriogenology.2011.10.025. Epub 2011 Dec 6.
This study investigated the effects of porcine granulocyte-macrophage colony-stimulating factor (pGM-CSF) on the developmental potential of porcine in vitro-fertilized (IVF) embryos in chemically and semidefined (with BSA) medium. In experiment 1, zygotes were treated with different concentrations of pGM-CSF (0, 2, 10, 100 ng/mL). The results indicated that 10 ng/mL pGM-CSF significantly (P < 0.05) increased blastocyst development and total cell number (15.1% and 53.5, respectively) compared with the control (6.1%, and 38.8, respectively). Comparing blastocyst formation, early and expanded blastocyst formation was significantly higher in the 10 ng/mL-pGM-CSF group than in the control on Days 6 and 7 of the culture period. However, there was no significant difference in cleavage rate. Experiment 2 demonstrated that pGM-CSF influenced the percentage of blastocyst formation and total cell number when pGM-CSF was added during Days 4 to 7 (14.6% and 53.9, respectively) or Days 0 to 7 (15.2% and 54.0, respectively) compared with the control (7.8% and 43.1, respectively) and compared with Days 0 to 3 (8.7% and 42.5, respectively). Similarly, early blastocyst formation rates were significantly higher at Days 4 to 7 than in the control, and expanded blastocyst formation was significantly higher at Days 4 to 7 or Days 0 to 7. No significant difference in cleavage rates appeared among the groups. In experiment 3, in the presence of BSA, pGM-CSF also increased the percentage of embryos that developed to the blastocyst stage and the total cell number (20.3% and 59.8, respectively) compared with the control (14.9% and 51.4, respectively), whereas there was no significant difference in cleavage rate. Experiment 4 found that the total cell number and the number of cells in the inner cell mass (ICM) were significantly increased compared with the control when zygotes were cultured in either porcine zygotic medium (PZM)-3 or PZM-4 supplemented with 10 ng/mL pGM-CSF. The number of trophectoderm (TE) cells was significantly higher in PZM-3 medium supplemented with pGM-CSF than in the control, and the number tended to increase (P = 0.058) in PZM-4 medium supplemented with pGM-CSF. The ratio of inner cell mass to trophectoderm cells was significantly higher in PZM-4 supplemented with 10 ng/mL pGM-CSF, but not in PZM-3. In experiment 5, it was found that the male pronuclear formation rate, monospermic penetration and sperm/oocyte were 95.4%, 37.2%, and 2.4, respectively. Together, these results suggest that pGM-CSF may have a physiological role in promoting the development of porcine preimplantation embryos and regulating cell viability and that addition of pGM-CSF to IVC medium at Days 4 to 7 or 0 to 7 improves the developmental potential of porcine IVF embryos.
本研究探讨了猪粒细胞-巨噬细胞集落刺激因子(pGM-CSF)在化学和半定义(含 BSA)培养基中对猪体外受精(IVF)胚胎发育潜力的影响。在实验 1 中,将胚胎分别用不同浓度的 pGM-CSF(0、2、10、100ng/mL)处理。结果表明,与对照组(分别为 6.1%和 38.8%)相比,10ng/mL pGM-CSF 显著(P<0.05)提高了囊胚发育和总细胞数(分别为 15.1%和 53.5%)。在培养第 6 天和第 7 天,与对照组相比,10ng/mL-pGM-CSF 组的囊胚形成率、早期囊胚形成率和扩张囊胚形成率均显著升高。然而,卵裂率没有显著差异。实验 2 表明,与对照组(分别为 7.8%和 43.1%)相比,pGM-CSF 在第 4 天至第 7 天(分别为 14.6%和 53.9%)或第 0 天至第 7 天(分别为 15.2%和 54.0%)添加时,对囊胚形成率和总细胞数有影响,与对照组相比,第 0 天至第 3 天(分别为 8.7%和 42.5%)添加时也有影响。同样,第 4 天至第 7 天的早期囊胚形成率显著高于对照组,第 4 天至第 7 天或第 0 天至第 7 天的扩张囊胚形成率显著高于对照组。各组之间卵裂率无显著差异。在实验 3 中,BSA 存在的情况下,pGM-CSF 也增加了胚胎发育至囊胚阶段的百分比和总细胞数(分别为 20.3%和 59.8%)与对照组(分别为 14.9%和 51.4%)相比,而卵裂率没有显著差异。实验 4 发现,与对照组相比,当胚胎在猪胚胎培养基(PZM)-3 或 PZM-4 中培养时,添加 10ng/mL pGM-CSF 可显著增加总细胞数和内细胞团(ICM)细胞数。添加 pGM-CSF 的 PZM-3 培养基中的滋养外胚层(TE)细胞数显著高于对照组,且有增加的趋势(P=0.058)。添加 pGM-CSF 的 PZM-4 培养基中的 TE 细胞数也有增加的趋势(P=0.064)。添加 10ng/mL pGM-CSF 的 PZM-4 中内细胞团与滋养外胚层细胞的比例显著升高,但在 PZM-3 中则没有。在实验 5 中,发现雄性原核形成率、单精子穿透和精子/卵子分别为 95.4%、37.2%和 2.4。综上所述,pGM-CSF 可能在促进猪胚胎着床前发育和调节细胞活力方面发挥生理作用,在第 4 天至第 7 天或第 0 天至第 7 天向 IVC 培养基中添加 pGM-CSF 可提高猪 IVF 胚胎的发育潜力。