Mitalipov S M, White K L, Farrar V R, Morrey J, Reed W A
Animal, Dairy and Veterinary Sciences Department, Center for Developmental and Molecular Biology, Biotechnology Center, Utah State University, Logan, Utah 84322-4815, USA.
Biol Reprod. 1999 Apr;60(4):821-7. doi: 10.1095/biolreprod60.4.821.
The present study was carried out to evaluate the effects of different activation protocols, enucleation methods, and culture media on the development of parthenogenetic and nuclear transfer (NT) rabbit embryos. Electroporation of 25 mM inositol 1,4, 5-trisphosphate (IP3) in calcium- and magnesium-free PBS immediately induced a single intracellular calcium transient in 6 out of 14 metaphase II-stage rabbit oocytes evaluated during a 10-min recording period. The percentage of oocytes treated with IP3 followed by 6-dimethylaminopurine (IP3 + DMAP) that cleaved (83.9%) and reached the blastocyst stage (50%) was significantly higher (p < 0.05) than those activated with multiple pulses (61.6% and 30.1%, respectively) or treated with ionomycin + DMAP (52.9% and 5.7%, respectively). Development of IP3 + DMAP-activated rabbit oocytes and in vivo-fertilized zygotes in different culture media was studied. Development of activated oocytes to the blastocyst stage in Earle's balanced salt solution (EBSS) supplemented with MEM nonessential amino acids, basal medium Eagle amino acids, 1 mM L-glutamine, 0.4 mM sodium pyruvate, and 10% fetal bovine serum (FBS) (EBSS-complete) (40.6%) was significantly higher (p < 0.05) than those that developed in either Dulbecco's Modified Eagle's medium (DMEM)/RPMI + 10% FBS (15.5%) or CR1aa + 10% FBS (4%) medium. In addition, 100% of in vivo-fertilized rabbit zygotes developed to the blastocyst stage in EBSS-complete. A third set of experiments was carried out to study the efficiency of blind versus stained (Hoechst 33342) enucleation of oocytes. Twenty-nine of 48 blind enucleated and IP3 + DMAP-activated oocytes cleaved (60.4%), and 15 (31.2%) subsequently reached the blastocyst stage, whereas 9 of 52 oocytes enucleated using epifluorescence (17.3%) cleaved, and none of these reached the blastocyst stage. When the above parameters that yielded the highest blastocysts were combined in an NT experiment using adult rabbit fibroblast nuclei, 72.2% (39 of 54) of the fused nuclear transplant embryos cleaved and 29.6% (16 of 54) reached the blastocyst stage.
本研究旨在评估不同激活方案、去核方法和培养基对孤雌生殖和核移植(NT)兔胚胎发育的影响。在无钙和镁的PBS中对25 mM肌醇1,4,5 -三磷酸(IP3)进行电穿孔处理,在10分钟的记录期内,14个中期II期兔卵母细胞中有6个立即诱导出单个细胞内钙瞬变。用IP3后接6 -二甲基氨基嘌呤(IP3 + DMAP)处理的卵母细胞的分裂率(83.9%)和发育到囊胚阶段的比例(50%)显著高于用多次脉冲激活的卵母细胞(分别为61.6%和30.1%)或用离子霉素+ DMAP处理的卵母细胞(分别为52.9%和5.7%)(p < 0.05)。研究了IP3 + DMAP激活的兔卵母细胞和体内受精合子在不同培养基中的发育情况。在补充了MEM非必需氨基酸、基础培养基鹰氨基酸、1 mM L -谷氨酰胺、0.4 mM丙酮酸钠和10%胎牛血清(FBS)的Earle平衡盐溶液(EBSS)(EBSS -完全培养基)中,激活的卵母细胞发育到囊胚阶段的比例(40.6%)显著高于在杜氏改良 Eagle培养基(DMEM)/RPMI + 10% FBS(15.5%)或CR1aa + 10% FBS(4%)培养基中发育的比例(p < 0.05)。此外,100%的体内受精兔合子在EBSS -完全培养基中发育到囊胚阶段。进行了第三组实验来研究卵母细胞盲目去核与染色(Hoechst 33342)去核的效率。48个盲目去核并经IP3 + DMAP激活的卵母细胞中有29个分裂(60.4%),其中15个(31.2%)随后发育到囊胚阶段,而52个采用落射荧光去核的卵母细胞中有9个(17.3%)分裂,但这些均未发育到囊胚阶段。当在使用成年兔成纤维细胞核的NT实验中结合上述产生最高囊胚率的参数时,72.2%(54个中的39个)的融合核移植胚胎分裂,29.6%(54个中的16个)发育到囊胚阶段。