荧光显微镜对早期牛胚胎活力的诊断

E. Schilling, D. Smidt, B. Sacher, D. Petac, S. Kaschab
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引用次数: 27

摘要

总结。荧光显微镜技术使用二乙酰荧光素(FDA)作为底物已经测试了早期牛胚胎的生存能力评估。将5 ~ 8天大的牛胚胎在含FDA浓度为1:40 000或1:80 000的PBS中室温孵育3 ~ 5分钟。然后在蔡司Axiomat显微镜下使用KP 490和520屏障滤光片对胚胎进行反射光荧光检测。体外培养24h后,用有丝分裂活性测定其生存能力。在FDA培养基中培养3分钟后,85 p. 100的荧光胚胎在培养后出现有丝分裂。没有一个非荧光胚胎在体外发育。一些胚胎(约6p . 100)含有死细胞和活细胞,这是通过FDA测试确定的;这些差异反应胚胎中有少数是可存活的,但大多数不是。胚胎在FDA培养基中短期孵育可能不会损害其发育,并且在FDA试验后移植的17至20日龄兔胎儿中未见致畸作用。
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Diagnosis of the viability of early bovine embryos by fluorescence microscopy
Summary. A fluorescence microscopy technique using diacetylfluorescin (FDA) as a substrate has been tested for the evaluation of the viability of early bovine embryos. Five to 8-day old cattle embryos were incubated in PBS containing FDA concentrations of 1 : 400 000 or 1 : 800 000 for 3 to 5 min at room temperature. Embryos were then examined by reflected light fluorescence using a KP 490 and 520 barrier filter in a Zeiss Axiomat microscope. Their mitotic activity after 24 hrs culture in vitro was used to determine their viability. After 3 min of incubation in the FDA medium, 85 p. 100 of the brilliantly fluorescing embryos showed mitoses after culture. None of the non-fluorescing embryos developed in vitro. Some embryos (about 6 p. 100) contained both dead and living cells as determined using the FDA test ; a few of these differentially reactive embryos were viable, but most of them were not. Short-term incubation of embryos in FDA medium probably did not impair their development, and no teratogenic effects could be seen in 17 to 20-day old rabbit fetuses transferred after the FDA test.
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