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Human embryonic development after blastomere removal: A time-lapse analysis

机译:去除卵裂球后的人类胚胎发育:延时分析

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BACKGROUND: Blastomere biopsy of human embryos is performed for preimplantation genetic diagnosis (PGD). The impact on further development is largely unexplored, though studies on mice suggest an influence on the hatching process. The objective of this study was to evaluate the effect of blastomere biopsy on early human embryonic development using time-lapse analysis. METHODS: Embryos from couples undergoing PGD treatment or IVF/ICSI were included. In the PGD group, 56 human embryos had one blastomere biopsied. As controls, 53 non-biopsied IVF/ICSI embryos were selected. All embryos were cultured until 5 days after fertilization in a time-lapse incubator (EmbryoScope?). Images of embryos were acquired every 20min. Time-points of key embryonic events were registered, and development in the two groups was compared. RESULTS: Duration of the biopsied cell-stage in the PGD group was longer than in the control group (P < 0.001), causing biopsied embryos to reach subsequent embryonic stages until hatching at significantly later time-points (Pcompaction < 0.001; Pmorula < 0.001; Pearlyblast < 0.001; Pfullblast 0.01), but with unchanged intervals. Embryos in the PGD group started hatching at the same time-point as the control group, but had a smaller diameter (P < 0.001), and a thicker zona pellucida (P < 0.001) when hatching. Time-lapse videos revealed that in the control group, expansion of the blastocyst caused continuous thinning of zona pellucida until the blastocyst hatched, whereas in the PGD group the blastocyst hatched through the opening in zona pellucida artificially introduced prior to the biopsy. CONCLUSIONS: We find that blastomere biopsy prolongs the biopsied cell-stage, possibly caused by a delayed compaction and alters the mechanism of hatching.
机译:背景:人类胚胎的卵裂球活检用于植入前遗传学诊断(PGD)。尽管对小鼠的研究表明对孵化过程有影响,但对进一步发育的影响尚待探索。这项研究的目的是使用延时分析来评估卵裂球活检对人类早期胚胎发育的影响。方法:包括接受PGD或IVF / ICSI治疗的夫妇的胚胎。在PGD组中,对56个人类胚胎进行了一次卵裂球活检。作为对照,选择了53个未活检的IVF / ICSI胚胎。将所有胚胎在定时孵化器(EmbryoScope?)中培养直至受精后5天。每20分钟获取一次胚胎图像。记录关键胚胎事件的时间点,并比较两组的发育情况。结果:PGD组的活检细胞期持续时间长于对照组(P <0.001),导致活检的胚胎到达随后的胚胎阶段,直到在较晚的时间点孵化(Pcompact <0.001; Pmorula <0.001)。 ; Pearlyblast <0.001; Pfullblast 0.01),但间隔不变。 PGD​​组的胚胎在与对照组相同的时间点开始孵化,但孵化时直径较小(P <0.001),透明带较厚(P <0.001)。延时录像显示,在对照组中,胚泡的膨胀会导致透明带一直变薄,直到囊胚孵出为止;而在PGD组中,胚泡是通过在活检之前人工引入的透明带开口孵出的。结论:我们发现卵裂球活检延长了活检的细胞阶段,这可能是由于压实延迟造成的,并且改变了孵化的机理。

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