| Literature DB >> 20819385 |
Toru Takeo1, Tomoko Kondo, Yukie Haruguchi, Kiyoko Fukumoto, Yoshiko Nakagawa, Yumi Takeshita, Yuko Nakamuta, Shuuji Tsuchiyama, Norihiko Shimizu, Takanori Hasegawa, Motohito Goto, Hitoshi Miyachi, Masayuki Anzai, Rie Fujikawa, Koji Nomaru, Takehito Kaneko, Yoshiaki Itagaki, Naomi Nakagata.
Abstract
At refrigerated temperatures, mouse embryos can maintain developmental ability for short periods. Previously, we succeeded in transporting vitrified and warmed 2-cell mouse embryos while maintaining developmental ability at refrigerated temperatures for 50 h. Transport of nonfrozen embryos is an easier and more useful means of exchanging genetically engineered mice between laboratories than is transport of cryopreserved embryos. Here we examined the developmental ability of transported 2-cell embryos that were produced through in vitro fertilization using cryopreserved sperm. Results show that 2-cell embryos produced by cryopreserved sperm can develop into blastocysts after cold storage for 24, 48, and 72 h. Transported 2-cell embryos produced by cryopreserved sperm yielded a favorable number of pups in all of the receiving laboratories after transport lasting 48 to 52 h. In summary, cold storage and transport of 2-cell embryos derived from cryopreserved sperm at refrigerated temperatures provides a novel means of transporting genetically engineered mice as an alternative to the transport of cryopreserved embryos and sperm.Entities:
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Year: 2010 PMID: 20819385 PMCID: PMC2919179
Source DB: PubMed Journal: J Am Assoc Lab Anim Sci ISSN: 1559-6109 Impact factor: 1.232