Yoshioka Koji, Suzuki Chie, Onishi Akira
National Institute of Animal Health, Tsukuba, Japan.
J Reprod Dev. 2008 Jun;54(3):208-13. doi: 10.1262/jrd.20001. Epub 2008 Apr 14.
We have previously indicated that porcine blastocysts can be produced by in vitro fertilization (IVF) and culture (IVC) in chemically defined porcine gamete medium (PGM) and porcine zygote medium (PZM)-5, respectively, In the present study, the effects of basic media and macromolecular components on in vitro maturation (IVM) were investigated to develop a defined system for in vitro embryo production using a single basic medium through IVM, IVF and IVC. Porcine immature oocytes were matured in porcine oocyte medium (POM) or modified North Carolina State University (mNCSU) 37, which were supplemented with either 10% (v/v) porcine follicular fluid (pFF) or 3 mg/ml polyvinyl alcohol (PVA) as a macromolecular component (designated POM+pFF, POM+PVA, mNCSU37+pFF and mNCSU37+PVA). In the maturation with mNCSU37+PVA, the percentages of oocytes that reached the metaphase II stages were significantly lower than those in the other treatments. Following IVM with the above media, oocytes were treated with an electrical stimulus and cycloheximide for parthenogenetic activation and were cultured in PZM-5 for 5 days. The rates of cleavage and blastocyst formation of parthenogenetic oocytes were significantly lowered for maturation with mNCSU37+PVA compared with the other treatments, while there were no significant differences in the total numbers of cells in blastocysts among the treatments. Following IVF and IVC, the rates of penetration, male pronucleus formation, cleavage and blastocyst formation were significantly lower when oocytes were matured in mNCSU37+PVA than in other maturation media. The normal fertilization rate was significantly higher in POM+PVA compared with the other treatments, although the total number of cells in blastocysts was reduced with the addition of PVA to both POM and mNCSU37 compared with pFF supplementation. These results demonstrate that porcine blastocysts can be produced by the defined system using a single basic medium.
我们之前指出,猪囊胚可分别通过在化学成分明确的猪配子培养基(PGM)和猪合子培养基(PZM)-5中进行体外受精(IVF)和培养(IVC)来产生。在本研究中,研究了基础培养基和大分子成分对体外成熟(IVM)的影响,以开发一种使用单一基础培养基通过IVM、IVF和IVC进行体外胚胎生产的明确系统。猪未成熟卵母细胞在猪卵母细胞培养基(POM)或改良的北卡罗来纳州立大学(mNCSU)37中成熟,这两种培养基分别添加了10%(v/v)猪卵泡液(pFF)或3 mg/ml聚乙烯醇(PVA)作为大分子成分(分别称为POM + pFF、POM + PVA、mNCSU37 + pFF和mNCSU37 + PVA)。在使用mNCSU37 + PVA进行成熟培养时,达到中期II阶段的卵母细胞百分比显著低于其他处理组。使用上述培养基进行IVM后,卵母细胞经电刺激和环己酰亚胺进行孤雌激活,并在PZM - 5中培养5天。与其他处理相比,使用mNCSU37 + PVA进行成熟培养的孤雌卵母细胞的卵裂率和囊胚形成率显著降低,而各处理组囊胚中的细胞总数没有显著差异。在进行IVF和IVC后,当卵母细胞在mNCSU37 + PVA中成熟时,其穿透率、雄原核形成率、卵裂率和囊胚形成率显著低于在其他成熟培养基中成熟的卵母细胞。与其他处理相比,POM + PVA中的正常受精率显著更高,尽管与添加pFF相比,在POM和mNCSU37中添加PVA后囊胚中的细胞总数减少。这些结果表明,使用单一基础培养基的明确系统可以产生猪囊胚。