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首页> 外文期刊>Molecular reproduction and development >Differential effect of recipient cytoplasm for microtubule organization and preimplantation development in rat reconstituted embryos with two-cell embryonic cell nuclear transfer
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Differential effect of recipient cytoplasm for microtubule organization and preimplantation development in rat reconstituted embryos with two-cell embryonic cell nuclear transfer

机译:受体细胞质对两细胞胚胎细胞核移植大鼠重构胚胎中微管组织和植入前发育的不同作用

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In the present study, we examined the developmental ability of enucleated zygotes, MII oocytes, and parthenogenetically activated oocytes at pronuclear stages (parthenogenetic PNs) as recipient cytoplasm for rat embryonic cell nuclear transfer. Enucleated zygotes as recipient cytoplasm receiving two-cell nuclei allowed development to blastocysts, whereas the development of embryos reconstituted with MII oocytes and parthenogenetic PNs was arrested at the two-cell stage. Previous observations in rat two-cell embryos suggested that the distribution of microtubules is involved in two-cell arrest. Therefore, we also examined the distribution of microtubules using immunofluorescence. At the two-cell stage after nuclear transfer into enucleated zygotes, microtubules were distributed homogeneously in the cytoplasm during interphase, and normal mitotic spindles were observed in cleaving embryos from the two- to four-cell stage. In contrast, embryos reconstituted with MII oocytes and parthenogenetic PNs showed aberrant microtubule organization. In enucleated zygotes, fibrous microtubules were distributed homogeneously in the cytoplasm. In contrast, dense microtubules were localized at the subcortical area in the cytoplasm and strong immunofluorescence intensity was observed at the plasma membrane, while very weak intensity was detected in the central part of enucleated MII oocytes. In enucleated parthenogenetic PNs, high-density and fibrous microtubules were distributed in the subcortical and central areas, respectively. Pre-enucleated parthenogenetic PNs also showed lower intensity of microtubule immunofluorescence in the central cytoplasm than zygotes. In conclusion, the results of the present study showed that zygote cytoplasm is better as recipient than MII oocyte and parthenogenetic PNs for rat two-cell embryonic cell nuclear transfer to develop beyond four-cell stage, Furthermore, microtubule organization is involved in the development of reconstituted embryos to overcome the two-cell arrest
机译:在本研究中,我们检查了去核合子,MII卵母细胞和孤核活化卵母细胞在原核阶段(孤雌生殖PNs)作为大鼠胚胎细胞核转移的受体细胞质的发育能力。作为接受两细胞核的受体细胞质的有核合子允许发育为胚泡,而用MII卵母细胞和孤雌生殖PNs重构的胚胎的发育则被阻滞在两细胞阶段。先前在大鼠两细胞胚胎中的观察表明,微管的分布与两细胞阻滞有关。因此,我们还使用免疫荧光检查了微管的分布。在核转移到去核的受精卵后的两细胞阶段,微管在相间期均匀地分布在细胞质中,并且从两细胞到四细胞阶段分裂的胚胎中观察到正常的有丝分裂纺锤体。相反,用MII卵母细胞和孤雌性PNs重构的胚胎显示出微管组织异常。在去核合子中,纤维微管均匀地分布在细胞质中。相反,致密的微管位于细胞质的皮层下区域,在质膜上观察到强的免疫荧光强度,而在去核的MII卵母细胞的中央部分检测到非常弱的强度。在去核的孤雌性PN中,高密度和纤维性微管分别分布在皮层下和中央区域。预去核孤雌生殖PNs还显示比合子更低的中央细胞质中的微管免疫荧光强度。总之,本研究的结果表明,受精卵细胞质比MII卵母细胞和孤雌性PNs更适合作为受体,从而使大鼠两细胞胚胎细胞的核移植发展到四细胞阶段以外,而且微管组织参与了细胞的发育。重构胚胎以克服两细胞阻滞

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