聚乙烯醇对小鼠着床前胚胎体外发育的支持作用

F. Koyanagi, S. Masuda
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引用次数: 2

摘要

研究了聚乙烯醇(PVA)对小鼠着床前胚胎发育的影响。在添加0.1或1.0 mg/ml PVA的Hoppe和Pitts培养基中,小鼠1细胞胚胎发育到膨大囊胚期的比例很高(与添加bsa的培养基相当)。然而,在添加10.0 mg/ml PVA的培养基中,没有胚胎发育到囊胚期。这些结果表明,在最佳浓度下,PVA支持胚胎从1细胞发育到囊胚期,PVA补充培养基是一种有价值的化学定义的小鼠胚胎培养培养基。此外,在本研究中,在添加pva的培养基中,胚胎从1细胞、2细胞、8细胞和早期囊胚阶段到囊胚膨大阶段的发育百分比和速度与添加bsa的培养基几乎相同。这些结果表明,这些胚胎通过正常过程发育为膨大囊胚,PVA支持胚胎在每个阶段直至膨大囊胚阶段的发育。在添加pva的培养基中,从1细胞阶段到囊胚早期,每个胚胎的囊胚部分孵化和完全孵化的发生率明显降低。有研究认为,蛋白酶可能参与囊胚的体外孵化过程,因此,在添加pva的培养基中,囊胚的低孵化率可能是由于蛋白酶的合成和/或分泌减少所致。
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Efficacy of Polyvinyl Alcohol Supporting the Development of Mouse Preimplantation Embryo In Vitro
The effect of polyvinyl alcohol (PVA) on the development of mouse preimplantation embryos was examined. In Hoppe and Pitts medium supplemented with 0.1 or 1.0 mg/ml PVA, a high percentage (comparable to BSA-supplemented medium) of mouse 1-cell embryos developed to the expanded blastocyst stage. However, in medium supplemented with 10.0 mg/ml PVA, no embryos developed to the blastocyst stage. These results indicate that, at optimum concentration, PVA supports embryo development from the 1-cell to the expanded blastocyst stage, and that the PVA-supplemented medium is a valuable chemically defined medium for mouse embryonic culture. Also, in this study, in the PVA-supplemented medium, percentages and speeds of embryo development from each stage (1-cell, 2-cell, 8-cell and early blastocyst) to the expanded blastocyst stage were almost the same as those in the BSA-supplemented medium. These results suggest that these embryos developed to expanded blastocysts via normal processes, and that PVA supports embryo development in each stage up to the expanded blastocyst stage. Incidence of partial hatching and complete hatching of blastocysts was clearly decreased in cultures of each embryo from 1-cell to the early blastocyst stage in the PVA-supplemented medium. It has been considered that protease may participate in the hatching process of blastocysts in vitro, thus, it is probable that the low hatching rate of blastocysts in the PVA-supplemented medium is due to a decline in protease synthesis and/or secretion.
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