Huang Wu-Jian, Yuan Jin, Deng Xing, An Jing
Department of Histology and Embryology, Southern Medical University, Guangzhou 510515, China.
Di Yi Jun Yi Da Xue Xue Bao. 2005 Mar;25(3):256-61.
To solve the problem known as 2-cell block in in vitro culture of preimplantation embryos, modification of the nutritional components in potassium simplex optimized medium (KSOM) was attempted and the preimplantation development and cleavage of mouse embryos in such medium observed.
One-cell mouse embryos collected from the oviduct of the superovulated mice were cultured in microdrops of different culture media for 5 days [144 h after human chorionic gonadotrophin (hCG) injection], and the percentages of embryos developed to pre-blastocyst, unhatched blastocyst, partially hatched blastocyst and completely hatched blastocyst were recorded at deferent time points (96, 120 and 144 h post-hCG) and total cell number of blastocysts at 120 h post-hCG counted. With these indices as the evaluation criteria, we evaluated the modifications of the concentrations of glucose (0.2, 5.56 mmol/l), bovine serum albumin (BSA, 1 and 4 mg/ml), and amino acids (1/2X NEAA and EAA, or not) in KSOM for their effect on the development of Kunming mouse zygotes in vitro.
Increasing the concentration of glucose and BSA was not shown to have significant effects on the rate of blastocyst formation at 120 h post-hCG or the total cell counts in KSOM without amino acids. After supplementation of the medium with amino acids, the rate of partially and completely hatched blastocyts was significantly increased in KSOM or KSOM supplemented with high concentrations of glucose and BSA (KSOMGB). Glucose at the high concentration of 5.56 mmol/L did not inhibit the development of mouse zygotes to hatched blastocysts cultured in KSOM supplemented with amino acids.
Increasing the concentration of glucose and BSA and amino acids in KSOM can promote the preimplantation development of mouse zygotes in in vitro culture.
为解决着床前胚胎体外培养中的2-细胞阻滞问题,尝试对单钾离子优化培养基(KSOM)中的营养成分进行改良,并观察小鼠胚胎在此种培养基中的着床前发育及分裂情况。
从超排卵小鼠的输卵管中收集单细胞小鼠胚胎,在不同培养基的微滴中培养5天[人绒毛膜促性腺激素(hCG)注射后144小时],并在不同时间点(hCG注射后96、120和144小时)记录发育至前囊胚、未孵化囊胚、部分孵化囊胚和完全孵化囊胚的胚胎百分比,同时计数hCG注射后120小时囊胚的总细胞数。以这些指标作为评估标准,我们评估了KSOM中葡萄糖(0.2、5.56 mmol/L)、牛血清白蛋白(BSA,1和4 mg/ml)以及氨基酸(1/2X非必需氨基酸和必需氨基酸,或无)浓度的改良对昆明小鼠合子体外发育的影响。
在不含氨基酸的KSOM中,提高葡萄糖和BSA的浓度对hCG注射后120小时的囊胚形成率或总细胞计数未显示出显著影响。在培养基中添加氨基酸后,KSOM或添加高浓度葡萄糖和BSA的KSOM(KSOMGB)中部分和完全孵化囊胚的比率显著增加。5.56 mmol/L的高浓度葡萄糖并未抑制在添加氨基酸的KSOM中培养的小鼠合子发育至孵化囊胚。
提高KSOM中葡萄糖、BSA和氨基酸的浓度可促进小鼠合子在体外培养中的着床前发育。