作者: T. Tani , Y. Kato , Y. Tsunoda
DOI: 10.1016/S0093-691X(00)00302-2
关键词: Embryo 、 Cytoplast 、 Biology 、 Somatic cell 、 Mitosis 、 Molecular biology 、 Nucleus 、 Cryopreservation 、 Andrology 、 Blastocyst 、 In vitro
摘要: An efficient method for freezing donor cells is necessary when using nucleus transfer of somatic large-scale cloning. In the present study, we developed a and thawing bovine cumulus cell-derived cultured to be used as donors. Cumulus were obtained from ovaries living slaughtered in vitro. serum-starved several days induce quiescent state then frozen at -70 degrees C least 2 d. Immediately thereafter or h after thawing, nuclear without additional vitro culture. The fusion rate with recipient cytoplasts was not affected by cell source (slaughtered living) time (0 h). cleavage frozen-thawed cows immediately h) highest (97%) significantly higher than that controls (85%) transferred (85%). There no significant differences among any groups potential embryos develop into blastocysts (34 vs 44 44%, 39 45 46%). Thus, storage effective might useful convenient maximum periods developmental such transfers requires further examination.