Takagi M, Sakonju I, Suzuki T
United Graduate School of Veterinary Science, Yamaguchi University, Japan.
J Vet Med Sci. 1996 Dec;58(12):1237-8. doi: 10.1292/jvms.58.12_1237.
The rate of DNA synthesis in the inner cell mass (ICM) of frozen-thawed bovine embryos was examined. Bovine blastocysts derived from in vitro matured/in vitro fertilized oocytes were frozen with 1.8 M ethylene glycol (EG), 1.6 M propylene glycol (PG) and 1.4 M glycerol plus 0.25 M sucrose (GL). Viable embryos, after thawing and culture beyond the blastocysts stage, were examined by immunocytochemical staining for detection of DNA synthesis by ICM cells. The numbers of bromodeoxyuridine-immunoreactive ICM cells of frozen-thawed embryos prepared with EG (10.7) and GL (11.5) were significantly lower than those of unfrozen embryos (17.3). The results suggest that the rates of proliferation of ICM cells of frozen-thawed bovine embryos tend to be lower than those of unfrozen embryos irrespective of the cryoprotectant used.
对冻融牛胚胎内细胞团(ICM)中的DNA合成速率进行了检测。将体外成熟/体外受精卵母细胞来源的牛囊胚用1.8M乙二醇(EG)、1.6M丙二醇(PG)和1.4M甘油加0.25M蔗糖(GL)进行冷冻。解冻并培养至囊胚期以上的存活胚胎,通过免疫细胞化学染色检测ICM细胞的DNA合成。用EG(10.7)和GL(11.5)制备的冻融胚胎中,溴脱氧尿苷免疫反应性ICM细胞的数量显著低于未冷冻胚胎(17.3)。结果表明,无论使用何种冷冻保护剂,冻融牛胚胎ICM细胞的增殖速率都倾向于低于未冷冻胚胎。