Center of Reproductive Medicine, the First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Sci China Life Sci. 2012 Apr;55(4):349-57. doi: 10.1007/s11427-012-4309-8. Epub 2012 May 9.
Cryopreservation of spermatozoa is a strategy that has been used to conserve the sperm of animal species and animal strains that are valuable for biomedical research. A simple method for preserving spermatozoa after application of intracytoplasmic sperm injection (ICSI) is much needed. It has been shown previously that spermatozoa frozen at -20°C can activate oocytes and support full-term embryo development. However, epigenetic reprogramming could be affected by the environment and by the in vitro manipulation of gametes. Here, we investigated embryo epigenetic reprogramming including DNA methylation and histone modification, in embryos derived from sperm preserved at -20°C without cryoprotectants. The results showed that although both fertilization and embryo developmental competence were decreased, the dynamic epigenetic reprogramming of embryos derived from frozen sperm was similar to the reprogramming of embryos derived from fresh sperm. The results reported in this study indicate that sperm frozen without cryoprotectant is epigenetically safe for ICSI.
精子的冷冻保存是一种被用于保存对于生物医学研究有价值的动物物种和动物品系的精子的策略。非常需要一种在应用胞浆内单精子注射 (ICSI) 后保存精子的简单方法。先前已经表明,在-20°C 下冷冻的精子可以激活卵母细胞并支持足月胚胎发育。然而,表观遗传重编程可能会受到环境和配子体外操作的影响。在这里,我们研究了胚胎的表观遗传重编程,包括 DNA 甲基化和组蛋白修饰,这些胚胎来自于未经冷冻保护剂保存的-20°C 下的精子。结果表明,尽管受精和胚胎发育能力都降低了,但来自冷冻精子的胚胎的动态表观遗传重编程与来自新鲜精子的胚胎的重编程相似。本研究的结果表明,未经冷冻保护剂冷冻的精子在 ICSI 方面是安全的。