Kato Y, Tsunoda Y
Laboratory of Animal Reproduction, College of Agriculture, Kinki University Nara 631, Japan.
Theriogenology. 1994;41(6):1315-22. doi: 10.1016/0093-691x(94)90490-a.
Different numbers of CD-1 mouse zygotes(1, 5, 10, 20, 40 and 60) were cultured in 10 mul M16 medium, in M16 medium+EDTA, in M16 dedium+SOD+thioredoxin, and in CZB medium, respectively. When the zygotes, regardless of the number, were cultured with M16, no blastocysts could be obtained. The suitable ratio of embryos to 1 mul of M16 medium+EDTA or M16 medium+SOD+thioredoxin was 1:1 or 2:1. Medium volume from 1 to 10 mul did not affect blastocyst development when the embryo density was 1:1. However, blastocysts obtained from zygotes cultured singly had fewer cell numbers and showed inferior development to live fetuses after transfer to recipients. When CZB medium was used, suitable embryo density was not clear. The ratio of embryos to volume of culture medium was shown to be an important factor for in vitro culture of mouse zygotes.
将不同数量的CD-1小鼠受精卵(1、5、10、20、40和60个)分别培养于10微升M16培养基、M16培养基+乙二胺四乙酸(EDTA)、M16培养基+超氧化物歧化酶(SOD)+硫氧还蛋白中,以及CZB培养基中。当无论数量多少的受精卵用M16培养基培养时,均无法获得囊胚。对于1微升M16培养基+EDTA或M16培养基+SOD+硫氧还蛋白而言,合适的胚胎与培养基比例为1:1或2:1。当胚胎密度为1:1时,1至10微升的培养基体积不影响囊胚发育。然而,单独培养的受精卵获得的囊胚细胞数量较少,且移植到受体后与活胎相比发育较差。当使用CZB培养基时,合适的胚胎密度不明确。胚胎与培养基体积的比例被证明是小鼠受精卵体外培养的一个重要因素。