Research and Development Group, Zen-noh Embryo Transfer Center, Kamishihoro, Hokkaido 080-1407, Japan.
Sci Rep. 2013;3:1173. doi: 10.1038/srep01173. Epub 2013 Jan 30.
Cryopreservation methods using liquid nitrogen (LN(2)) for gametes and embryos are prevalent in mammalian artificial reproduction. However, the pregnancy rate from frozen embryos has not improved over the past two decades because freeze-thawing causes significant damage. The strict regulation of transportation of LN(2) containers by airlines also limits exchange between breeders. In this article, we introduce a medium that enabled bovine embryos to be held for up to 7 days at 4°C. A pregnancy rate of 75% (24/32) was obtained for embryos held for 7 days in this medium and transferred to primed recipients. Its constituents were medium 199, foetal bovine serum, and HEPES for buffering. This technique will enable LN(2)-free storage and air transportation of embryos provided transplantation to recipients can be completed within 7 days.
使用液氮(LN(2)) 对配子和胚胎进行冷冻保存的方法在哺乳动物人工繁殖中很流行。然而,过去 20 年来,冷冻胚胎的妊娠率并没有提高,因为冷冻-解冻会造成严重的损伤。航空公司对 LN(2) 容器运输的严格规定也限制了饲养员之间的交流。在本文中,我们介绍了一种可以使牛胚胎在 4°C 下保存长达 7 天的培养基。在这种培养基中保存 7 天的胚胎的妊娠率为 75%(24/32),并将其转移到预先处理的受体中。其成分是培养基 199、胎牛血清和 HEPES 缓冲液。这项技术将使胚胎能够在没有 LN(2) 的情况下储存和空运,只要在 7 天内完成移植即可。