Dyban A P, Sekirina G G
Ontogenez. 1981;12(2):130-9.
2-celled mouse embryos F1 (CBA X C57B1) and ICR were divided to separate blastomeres. The sister blastomeres were cultivated for 3 days in microdrops of synthetic medium under the layer of mineral oil. The development of twin embryos attained the late blastocyst stage. Vital observations of the cleavage of sister blastomeres were carried out, and the cells of twin embryos were calculated on slides. Sometimes the twin embryos contained the same number of cells but, as a rule, the number of cells did not coincide, i. e. the descendants of sister blastomeres differed by the cleavage rate. Possible causes of this phenomenon are discussed.
将F1(CBA×C57B1)和ICR的2细胞期小鼠胚胎分离为单个卵裂球。将姐妹卵裂球在矿物油层下的合成培养基微滴中培养3天。双胚胎发育至晚期囊胚阶段。对姐妹卵裂球的分裂进行了活体观察,并在载玻片上对双胚胎的细胞进行了计数。有时双胚胎的细胞数量相同,但通常情况下,细胞数量并不一致,即姐妹卵裂球的后代在分裂速率上存在差异。文中讨论了这种现象可能的原因。