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首页> 外文期刊>Journal of the American Association for Laboratory Animal Science >Continuous Observation of Rabbit Preimplantation Embryos In Vitro by Using a Culture Device Connected to a Microscope
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Continuous Observation of Rabbit Preimplantation Embryos In Vitro by Using a Culture Device Connected to a Microscope

机译:通过使用连接到显微镜的培养设备连续观察兔体外植入前胚胎

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摘要

We developed a compact culture device that maintains developing embryos in vitro under constant temperature and CO2 concentration. Using this device, we cultured rabbit embryos from the pronuclear stage to the hatched blastocyst stage and recorded their development digitally for 7 d. Recorded images were converted to a movie, and the developmental movement of individual embryos was analyzed. With this culture system, we can observe embryonic development in a suitable environment continuously for several days; similar long-term observation is not possible in the conventional system. The proportion of embryos that developed from the pronuclear stage to the blastocyst stage was the same in the new system (73.1%; 38 of 52) as in the conventional (control) system (77.6%; 38 of 49). Compaction of embryos occurred from the 8-cell to the morula stage at 32.5 +/- 0.71 h after insemination. The time of blastocyst formation (77.2 +/- 3.2 h after insemination) varied somewhat between embryos. Average hatching time was 98.7 +/- 4.4 h after mating. Therefore, the cleavage, blastomere movement, and hatching processes of blastocysts can be followed clearly and recorded by using this new culture system.
机译:我们开发了一种紧凑型培养装置,可在恒温和CO2浓度下在体外维持发育中的胚胎。使用该设备,我们培养了从原核阶段到孵化的胚泡阶段的兔胚胎,并数字记录了它们的发育7 d。将记录的图像转换成电影,并分析单个胚胎的发育运动。通过这种培养系统,我们可以在合适的环境中连续观察几天的胚胎发育。在常规系统中不可能进行类似的长期观察。在新系统中,从原核阶段发展到胚泡阶段的胚胎比例(73.1%; 52个中的38个)与常规(对照)系统中相同(77.6%; 49个中的38个)。授精后的32.5 +/- 0.71小时,从8细胞期到桑ula期开始压实胚。胚泡形成的时间(受精后77.2 +/- 3.2小时)在胚胎之间有所不同。交配后平均孵化时间为98.7 +/- 4.4小时。因此,使用这种新的培养系统可以清楚地观察并记录囊胚的分裂,卵裂球运动和孵化过程。

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