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Nuclear and cytoskeletal dynamics during oocyte maturation and development of somatic cell cloned pig embryos injected with membrane disintegrated donor cells

机译:卵细胞成熟过程中的核和细胞骨架动力学以及注射了膜崩解性供体细胞的体细胞克隆猪胚胎的发育

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The objectives of this study were to characterize the nuclear and cytoskeletal changes of pig oocytes during in vitro maturation (IVM) and the development of the reconstructed embryos after injection with membrane intact or disintegrated donor cells. Cumulus-oocyte complexes (COCs) were collected from abattoir ovaries by follicle (2-8mm) aspiration. In Experiment 1, COCs were cultured in NCSU-23 medium for 0, 11, 22, 33, and 44h. Oocytes were fixed at different time points for nuclear and cytoskeletal labeling. Forty-three percent and 75% oocytes progressed to MII stage at 33 and 44h after IVM culture, respectively. Dynamic shift of spindle and cytoplasmic microtubules was evident. In Experiment 2, matured oocytes were injected with either the whole cumulus cell with or without intact cell membranes after enucleation. The reconstructed oocytes were fixed at 0, 2, or 4h after cell injection for nuclear and cytoskeletal evaluation. When an intact cumulus cell was injected, the injected cell remained intact within 4h after injection. When a cell with disintegrated membrane was injected, 59-63% (n=146) of the injected cell underwent premature chromosome condensation (PCC). In Experiment 3, the reconstructed pig oocytes received membrane-disintegrated cumulus cells or fetal fibroblasts were cultured in PZM medium. The blastocyst rate of the fibroblast-injected embryos was 10%, which was lower than the non-cloned parthenotes (33%, P<0.05) but higher than the cumulus cell-injected embryos (2.7%). These results suggest that pig oocytes are subjected to nuclear and cytoskeletal reorganization during maturation. Pig oocytes injected with membrane-disintegrated fibroblast cells support better blastocyst development of the cloned embryos.
机译:这项研究的目的是表征猪卵母细胞在体外成熟(IVM)过程中的核和细胞骨架变化,以及注射完整或分裂的供体细胞后重建胚胎的发育。通过卵泡(2-8mm)抽吸从屠宰场卵巢中收集卵母细胞复合物(COC)。在实验1中,将COC在NCSU-23培养基中培养0、11、22、33和44h。将卵母细胞固定在不同的时间点进行核和细胞骨架标记。在IVM培养后的33和44小时,分别有43%和75%的卵母细胞进入MII期。纺锤体和细胞质微管的动态转移是明显的。在实验2中,去核后,向成熟卵母细胞注射具有或不具有完整细胞膜的整个卵丘细胞。重建的卵母细胞在细胞注射后0、2或4h固定,用于核和细胞骨架评估。当注射完整的卵丘细胞时,注射的细胞在注射后4小时内保持完整。当注射具有分解膜的细胞时,注射的细胞中有59-63%(n = 146)经历了早染色体凝集(PCC)。在实验3中,在PZM培养基中培养接受了膜分解的卵丘细胞或胎儿成纤维细胞的重建的猪卵母细胞。成纤维细胞注射的胚的胚泡率是10%,低于未克隆的单性生殖(33%,P <0.05),但高于卵丘细胞注射的胚(2.7%)。这些结果表明,猪卵母细胞在成熟过程中会经历核和细胞骨架的重组。注射有膜分解成纤维细胞的猪卵母细胞支持克隆胚胎更好的胚泡发育。

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