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首页> 外文期刊>Zygote >Spindle and chromosome configuration analysis of human biopsied versus non-biopsied embryos by confocal laser scanning microscopy following vitrification
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Spindle and chromosome configuration analysis of human biopsied versus non-biopsied embryos by confocal laser scanning microscopy following vitrification

机译:玻璃化后共聚焦激光扫描显微镜通过共聚焦激光扫描显微镜对人体活组织检查与非活检胚胎的纺织和染色体配置分析

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The aim of this study was to investigate the effects of zona drilling and biopsy on day 3 followed by vitrification on day 5 on the cytoskeleton and development of human embryos, by analysing survival rates and spindle and chromosome configurations by fluorescence and confocal laser scanning microscopy in human biopsied and non-biopsied embryos. In total, 98 human blastocysts (50 non-biopsied and 48 following biopsy on day 3) were vitrified on day 5 using either a commercial dimethyl sulphoxide (DMSO)-free vitrification kit or increasing concentrations of DMSO/EG (5%/5-10%/10-20%/20%). Following warming, the blastocysts were allowed to recover in culture for 24 h and were immunostained with alpha-tubulin, acetylated tubulin, and/or gamma-tubulin antibodies in combination with 4 ',6-diamidino-2-phenylindole (DAPI). Labelled embryos were examined by both fluorescence and confocal laser scanning microscopy. The survival rates following warming (92% non-biopsied vs 83.3% biopsied) and the incidence of normal spindle chromosome configurations was not statistically different between the two groups (65.2% non-biopsied vs 59.2% biopsied, P>0.05). The incidence of spindle abnormalities including multipolarity, chromosome lagging, congression failure and chromosome bridging were also similar between the two groups (P>0.05). This study is the first to compare the incidence of cytoskeletal abnormalities in biopsied and non-biopsied human embryos following vitrification. We conclude that there was no significant difference in the survival rates and the incidence of spindle abnormalities between the two groups.
机译:本研究的目的是研究Zona钻井和活检在第3天的作用,然后在第5天玻璃化对人骨折的第5天,通过荧光和共焦激光扫描显微镜分析存活率和牙线和染色体构造人类活检和非活检胚胎。总共有98例人胚泡(第3天在第3天发生的50个非活检和48天)在第5天玻璃化使用商业二甲基硫氧化物(DMSO) - 过量玻璃化试剂盒或增加DMSO /例如(5%/ 5- 10%/ 10-20%/ 20%)。在变暖之后,使胚泡在培养物中恢复24小时,并用α-微管蛋白,乙酰化小管蛋白和/或γ-管蛋白抗体与4',6-二脒基-2-苯基吲哚(DAPI)一起免疫染色。通过荧光和共聚焦激光扫描显微镜检查标记的胚胎。变暖后的存活率(92%非活检与83.3%的活检)和正常主轴染色体配置的发生率在两组之间没有统计学不同(65.2%非活检Vs 59.2%活检,P> 0.05)。两组(P> 0.05)之间也相似,包括多极性,染色体滞后,国会失效和染色体桥接等纺锤体异常的发生率。本研究是第一个比较玻璃化后体检和非活检人胚胎中细胞骨骼异常的发生率。我们得出结论,两组梭形异常的存活率没有显着差异。

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