Ruffing N A, Steponkus P L, Pitt R E, Parks J E
Department of Animal Science, Cornell University, Ithaca, New York 14853-5701.
Cryobiology. 1993 Dec;30(6):562-80. doi: 10.1006/cryo.1993.1059.
Bovine oocytes that were immature (IMM), matured in vitro (IVM) or in vivo (MAT), or matured and fertilized in vitro (IVF) were studied using a microscope diffusion chamber to estimate osmotic parameters and a cryomicroscope to characterize intracellular ice formation (IIF). Linear Boyle van't Hoff relationships were observed with all four types of oocytes between 0.265 and 0.799 osm NaCl. At 20 degrees C, estimates of hydraulic conductivity (Lp) were significantly higher for IVM oocytes than IMM and MAT oocytes (0.84 micron/(min.atm) vs 0.45 and 0.47, respectively). IVM oocytes also tended to have higher Lp values than IVF oocytes (0.55 micron/(min.atm)). At 5 degrees C, the Lp of IVM oocytes decreased to 0.36 micron/min.atm) corresponding to an Arrhenius activation energy of 7.84 kcal/mol. The incidence of IIF in MAT oocytes suspended in salt solution and subjected to linear cooling to -60 degrees C was 45% at 4 degrees C/min, 75% at 8 degrees C/min, and 93% at 16 degrees C/min; with IVF oocytes, the incidence of IIF was 40% at 4 degrees C/min, 92% at 8 degrees C/min, and 100% at 16 degrees C/min. Comparisons involving median IIF temperatures (TIIF50s) and the distributions of the observed IIF temperatures for IMM (Myers et al., Cryo-Lett. 8, 260), IVM (Chandrasekaran et al., Cryobiology 27, 676), MAT and IVF oocytes indicated that the IIF incidence in IMM oocytes cooled at 4 degrees C/min was greater than that of oocytes at the other developmental stages cooled at the same rate. The TIIF50s of IVM and IVF oocytes were lowered by equilibration in 1.5 M ethylene glycol (EG), glycerol, or propylene glycol (PG) prior to cooling, with EG tending to lower the TIIF50s more than glycerol or PG. For all three cryoprotectants, the TIIF50s and IFF temperature distributions were cooling-rate dependent. The Weibull probability distribution was fitted to the distributions of the IIF temperatures of oocytes suspended in salt solutions with and without cryoprotectants yielding R2 values ranging from 0.70 to 0.98.
使用显微镜扩散室估计渗透参数,并使用低温显微镜表征细胞内冰形成(IIF),对未成熟(IMM)、体外成熟(IVM)或体内成熟(MAT)、或体外成熟并受精(IVF)的牛卵母细胞进行了研究。在0.265至0.799渗透压的NaCl范围内,观察到所有四种类型的卵母细胞均呈现线性玻意耳-范特霍夫关系。在20℃时,IVM卵母细胞的水力传导率(Lp)估计值显著高于IMM和MAT卵母细胞(分别为0.84微米/(分钟·大气压),而IMM和MAT卵母细胞分别为0.45和0.47)。IVM卵母细胞的Lp值也往往高于IVF卵母细胞(0.55微米/(分钟·大气压))。在5℃时,IVM卵母细胞的Lp降至0.36微米/(分钟·大气压),对应的阿累尼乌斯活化能为7.84千卡/摩尔。悬浮在盐溶液中并以线性方式冷却至-60℃的MAT卵母细胞,在4℃/分钟的冷却速率下IIF发生率为45%,在8℃/分钟时为75%,在16℃/分钟时为93%;对于IVF卵母细胞,在4℃/分钟的冷却速率下IIF发生率为40%,在8℃/分钟时为92%,在16℃/分钟时为100%。涉及IMM(迈尔斯等人,《低温生物学通讯》8,260)、IVM(钱德拉塞卡兰等人,《低温生物学》27,676)、MAT和IVF卵母细胞的IIF中位温度(TIIF50s)以及观察到的IIF温度分布的比较表明,以4℃/分钟的速率冷却时,IMM卵母细胞中的IIF发生率高于以相同速率冷却的其他发育阶段的卵母细胞。在冷却前,将IVM和IVF卵母细胞在1.5 M乙二醇(EG)、甘油或丙二醇(PG)中平衡,可降低其TIIF50s,其中EG降低TIIF50s的程度往往大于甘油或PG。对于所有三种冷冻保护剂,TIIF50s和IFF温度分布均与冷却速率有关。将威布尔概率分布拟合到悬浮在有和没有冷冻保护剂的盐溶液中的卵母细胞的IIF温度分布,得到的R2值范围为0.70至0.98。