Departament de Medicina i Cirurgia Animals, Universitat Autònoma de Barcelona, Spain.
Cryobiology. 2014 Apr;68(2):288-93. doi: 10.1016/j.cryobiol.2014.02.010. Epub 2014 Feb 21.
Two experiments were designed to test the use of a new device designed to vitrify and in-straw warm in vitro produced (IVP) embryos, which can potentially be used for their direct transfer to recipient females in field conditions. In experiment 1, IVP embryos from both prepubertal and adult animals were vitrified on cryotops and warmed in steps (1, 0.5 and 0M sucrose; protocol W3) or directly in 0.5M (protocol W1/0.5) or 0M sucrose (protocol W1/0). Similar survival rates were recorded 24h after warming for calf embryos irrespective of the warming procedure (W3: 79.2%, W1/0.5: 62.5%, W1/0: 66.7%). For cow embryos, survival rates at 24h post-warming were significantly higher when embryos were warmed using the W3 (85.7%) or W1/0.5 (89.1%) protocols compared to the W1/0 protocol (70.5%). In experiment 2, IVP embryos were vitrified on the new designed device followed by their in-straw cryoprotectant (0.5M sucrose) dilution/warming and different warming temperatures (45, 50, 60 and 70°C) were tested. When warming solution passed through the new vitrification/warming device at 45°C, 61.5% of blastocysts were fully re-expanded or hatched at 24h post-warming, being not significantly different to the control (65%). Other warming temperatures triggered significantly lower survival rates at 24h post-warming. No significant differences were detected in total cell numbers and blastocyst apoptosis indices in response to vitrification followed by warming at 45°C respect to the control. Our findings indicate that the new device allows vitrification and in-straw warming of IVP bovine embryos, being a useful option for their direct transfer in field conditions.
设计了两项实验来测试一种新设备的使用效果,该设备旨在对体外生产(IVP)的胚胎进行玻璃化和 straw 内温化,这可能使其可在野外条件下直接用于受体雌性动物的胚胎移植。在实验 1 中,对来自未成年和成年动物的 IVP 胚胎进行 cryotop 玻璃化处理,并进行分步升温(1、0.5 和 0M 蔗糖;方案 W3)或直接在 0.5M(方案 W1/0.5)或 0M 蔗糖(方案 W1/0)中升温。无论升温程序如何(W3:79.2%,W1/0.5:62.5%,W1/0:66.7%),在升温后 24 小时,犊牛胚胎的存活率都相似。对于奶牛胚胎,与 W1/0 方案(70.5%)相比,使用 W3(85.7%)或 W1/0.5(89.1%)方案升温时,24 小时后胚胎的存活率显著更高。在实验 2 中,将 IVP 胚胎在新设计的设备上进行玻璃化处理,然后进行 straw 内 cryoprotectant(0.5M 蔗糖)稀释/升温,测试了不同的升温温度(45、50、60 和 70°C)。当升温溶液以 45°C 通过新的玻璃化/升温设备时,在升温后 24 小时,61.5%的囊胚完全重新扩张或孵化,与对照组(65%)没有显著差异。其他升温温度导致在升温后 24 小时的存活率显著降低。与对照组相比,玻璃化处理后在 45°C 下升温,胚胎的总细胞数和囊胚凋亡指数没有明显差异。我们的研究结果表明,该新型设备允许对 IVP 牛胚胎进行玻璃化和 straw 内升温,这是在野外条件下直接进行胚胎移植的一种有用选择。