Men Hongsheng, Agca Yuksel, Critser Elizabeth S, Critser John K
Department of Veterinary Pathobiology, University of Missouri-Columbia, MO 65211, USA.
Theriogenology. 2005 Oct 1;64(6):1340-9. doi: 10.1016/j.theriogenology.2005.02.013. Epub 2005 Apr 12.
The ability of porcine blastocysts produced in vitro, in the presence or absence of serum, to survive cryopreservation was investigated in this experiment. Porcine oocytes were matured, fertilized and cultured in vitro using serum-free culture systems. Starting at Day 4 of in vitro embryo culture (Day 0 = fertilization), the culture medium was supplemented with 10% fetal bovine serum (FBS). Embryos were cultured under these conditions until Day 6. Embryos cultured with only BSA supplementation served as serum-free controls. Day 6 blastocysts and expanded blastocysts of excellent quality were vitrified using the open pulled straw method. After warming, blastocysts were cultured in the presence of 10% FBS for an additional 18 h to recover. Portions of blastocysts from both groups, without cryopreservation, were also cultured under the same conditions to serve as non-vitrified controls. To further investigate the influence of FBS on the quality of embryos produced, the total cell numbers in Day 6 blastocysts from both groups were compared. In addition, the ratio of viable to total cells in fully recovered blastocysts at each group was examined. Blastocysts produced in the presence of FBS had an increased ability to survive cryopreservation and also had a higher cell number compared to those produced in serum-free systems (P < 0.05). The fully recovered blastocysts had a normal viable to total cell ratio, compared to non-vitrified controls. Overall, this experiment supports the hypothesis that serum supplementation during in vitro production of porcine embryos is beneficial to the ability of a blastocyst to survive cryopreservation.
本实验研究了在有或无血清存在的情况下体外产生的猪囊胚的冷冻保存存活率。猪卵母细胞在无血清培养系统中进行体外成熟、受精和培养。从体外胚胎培养第4天(第0天=受精)开始,培养基中添加10%胎牛血清(FBS)。胚胎在这些条件下培养至第6天。仅添加牛血清白蛋白(BSA)培养的胚胎作为无血清对照。使用开放式拉长细管法对第6天的优质囊胚和扩张囊胚进行玻璃化冷冻。解冻后,囊胚在10%FBS存在的情况下再培养18小时以恢复。两组未冷冻保存的部分囊胚也在相同条件下培养作为非玻璃化对照。为了进一步研究FBS对所产生胚胎质量的影响,比较了两组第6天囊胚的总细胞数。此外,还检查了每组完全恢复的囊胚中活细胞与总细胞的比例。与无血清系统产生的囊胚相比,在FBS存在下产生的囊胚冷冻保存存活率增加,并且细胞数也更高(P<0.05)。与非玻璃化对照相比,完全恢复的囊胚活细胞与总细胞比例正常。总体而言,本实验支持以下假设:在猪胚胎体外生产过程中添加血清有利于囊胚的冷冻保存存活率。