Westhusin M E, De Azambuja R M
Department of Veterinary Physiology and Pharmacology, Texas A & M University, College Station 77843, USA.
Anim Reprod Sci. 1996 Dec 2;45(1-2):29-35. doi: 10.1016/s0378-4320(96)01572-2.
This study was designed to evaluate the survival and development of in vitro derived bovine embryos following pronuclear transplantation and in vitro embryo culture. Bovine zygotes were produced by in vitro maturation and in vitro fertilization. Pronuclei were removed by micromanipulation and either transferred back to the same cell (Group 1) or into a previously enucleated zygote (Group 2) by electrofusion. Micromanipulated and non-micromanipulated (Group 3, control) zygotes were co-cultured with oviductal cells in a sealed modular chamber filled with 5% CO2, 5% O2 and 90% N2 at 39 degrees C for 7-8 days. Fusion rates were similar for Groups 1 and 2 (90.7 and 85.1%, respectively, P > 0.05). The percentage of embryos that cleaved was not different for Groups 1 (82.0%), 2 (90.0%) and 3 (76.9%, P > 0.05). Also, the percentage of embryos developing to the compact morula or blastocyst stage was similar (25.6, 22.5 and 22.3%, respectively, for Groups 1, 2 and 3, P > 0.05). The results of this experiment are the first to demonstrate that pronuclear transfer can be carried out successfully using bovine embryos derived from in vitro oocyte maturation and in vitro fertilization. In addition, pronuclei can be transferred from one bovine embryo to another and the reconstructed embryos develop to the compact morula and blastocyst stage in vitro. This technique, used in combination with oocyte retrieval by ultrasound-guided follicular aspiration and embryo transfer, offers the potential to study cytoplasmic inheritance in cattle directly, and to evaluate the effect of cytoplasmic inheritance on traits of economic importance.
本研究旨在评估原核移植后体外培养的牛胚胎的存活和发育情况以及体外胚胎培养情况。牛受精卵通过体外成熟和体外受精产生。通过显微操作去除原核,并通过电融合将其重新转移回同一个细胞(第1组)或转移到先前去核的受精卵中(第2组)。将经过显微操作和未经过显微操作的(第3组,对照组)受精卵与输卵管细胞在充满5%二氧化碳、5%氧气和90%氮气的密封模块化培养箱中于39℃共培养7 - 8天。第1组和第2组的融合率相似(分别为90.7%和85.1%,P>0.05)。第1组(82.0%)、第2组(90.0%)和第3组(76.9%,P>0.05)的胚胎分裂百分比没有差异。此外,发育到致密桑椹胚或囊胚阶段的胚胎百分比相似(第1组、第2组和第3组分别为25.6%、22.5%和22.3%,P>0.05)。本实验结果首次证明,使用体外卵母细胞成熟和体外受精获得的牛胚胎可以成功进行原核移植。此外,原核可以从一个牛胚胎转移到另一个胚胎,并且重构胚胎在体外发育到致密桑椹胚和囊胚阶段。该技术与超声引导卵泡抽吸获取卵母细胞和胚胎移植相结合,为直接研究牛的细胞质遗传以及评估细胞质遗传对经济重要性状的影响提供了可能性。