首页> 美国卫生研究院文献>Avicenna Journal of Medical Biotechnology >The Effect of Biopsy During Precompacted Morula Stage on Post Vitrification Development of Blastocyst Derived Bovine Embryos
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The Effect of Biopsy During Precompacted Morula Stage on Post Vitrification Development of Blastocyst Derived Bovine Embryos

机译:紧凑型桑ula胎期活检对玻璃化囊胚牛胚玻璃化后发育的影响

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摘要

Improvements on embryo micromanipulation techniques led to the use of embryo biopsy in commercial embryo transfer programs for genetic analysis of preimplantation bovine embryos. The aim of this study was to evaluate the quality of bovine blastocyst derived from embryos biopsied at different pre-compacted morulae stages by assessment of cryosurvivability of the resulting blastocysts. The in vitro produced bovine embryos were subjected to biopsy at days 2, 3, and 4 post-insemination with different cell numbers (4 to 16-cells). Embryo cell biopsy was carried out in a 100 µl drop of H-SOF following pronase drilling by aspiration of one blastomere. The biopsied embryos were then cultured in SOFaaBSA co-cultured with oviduct cells-monolayer until blastocyst formation. The blastocysts were cryopreserved at room temperature after exposure of equilibration (glycerol 1.4 M for 5 min and then glycerol 1.4 M and ethylene glycol 3.6 M for 5 min) and vitrification solutions (3.4 M glycerol and 4.6 M ethylene glycol). The blastocysts were loaded into the center of 0.25 ml straws separated by air bubbles from 2 columns of sucrose 0.5 M and plunged immediately into liquid nitrogen. There was no significant difference in cryosurvivability of vitrified-warmed blastocysts derived form biopsied embryos at different pre-compacted morula stages. The quality of biopsy derived blastocysts was identical to that of non-biopsy derived ones in terms of post vitrifcation survival and hatching rates. In conclusion there was no preference between different times of embryo biopsy at precompacted morula stages in term of cryosurvivability of biopsy derived bovine blastocysts.
机译:胚胎显微操作技术的改进导致在商业胚胎移植计划中使用胚胎活检进行植入前牛胚胎的遗传分析。这项研究的目的是通过评估所产生的胚泡的冷冻生存能力,来评估在不同的预先压实的桑e胚阶段活检的胚胎所产生的牛胚泡的质量。体外培养的牛胚胎在受精后第2、3和4天用不同的细胞数量(4至16个细胞)进行活检。链霉菌蛋白酶钻孔后,通过抽吸一个卵裂球,以100 µl的H-SOF液滴进行胚胎细胞活检。然后将活检的胚胎在与单层输卵管细胞共培养的SOFaaBSA中培养,直至形成胚泡。暴露平衡后,胚泡在室温下冷冻保存(1.4 M甘油5分钟,然后1.4 M甘油和3.6 M乙二醇5分钟)和玻璃化溶液(3.4 M甘油和4.6 M乙二醇)暴露。将胚泡装入0.25 ml吸管的中央,该吸管通过气泡从2根0.5 M蔗糖柱中分离,并立即注入液氮中。在预先压紧的桑ula鼠不同阶段,从活检的胚胎衍生的玻璃化温囊胚的冷冻生存能力没有显着差异。就玻璃化后存活率和孵化率而言,活检来源的胚泡的质量与非活检来源的胚泡的质量相同。总之,就活检来源的牛囊胚的冷冻生存能力而言,在预先压紧的桑ula鼠阶段,在不同时间的胚胎活检之间没有偏爱。

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