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Morphological and biochemical analysis of immature ovine oocytes vitrified with or without cumulus cells

机译:有或没有积云的玻璃化未成熟绵羊卵母细胞的形态学和生化分析

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The cryopreservation of oocytes is an open problem as a result of their structural sensitivity to the freezing process. This study examined (i) the survival and meiotic competence of ovine oocytes vitrified at the GV stage with or without cumulus cells; (ii) the viability and functional status of cumulus cells after cryopreservation; (iii) the effect of cytochalasin B treatment before vitrification; (iv) chromatin and spindle organization; (v) the maturation promoting factor (MPF) and mitogen-activated protein kinase (MAPK) activity of vitrified oocytes after in vitro maturation. Sheep oocytes were vitrified at different times during in vitro maturation (0, 2, and 6 h) with (COCs) or without cumulus cells (DOs). After warming and in vitro maturation, oocytes denuded at 0 h culture showed a significantly higher survival and meiotic maturation rate compared to the other groups. Hoechst 33342/propidium iodide double staining of COCs and microinjection of Lucifer Yellow revealed extensive cumulus cell membrane damage and reduced oocyte-cumulus cell communications after vitrification. Cytochalasin B treatment of COCs before vitrification exerted a negative effect on oocyte survival. After in vitro maturation, the number of vitrified oocytes with abnormal spindle and chromatin configuration was significantly higher compared to control oocytes, independently of the presence or absence of cumulus cells. The removal of cumulus cells combined with vitrification significantly decreased the MPF and MAPK levels. This study provides evidence that the removal of cumulus cells before vitrification enhances oocyte survival and meiotic competence, while impairing the activity of important proteins that could affect the developmental competence of oocytes.
机译:由于卵母细胞对冷冻过程的结构敏感性,其冷冻保存是一个未解决的问题。这项研究检查(i)在有或没有积云细胞的GV阶段玻璃化的绵羊卵母细胞的存活和减数分裂能力; (ii)冷冻保存后卵丘细胞的活力和功能状态; (iii)细胞松弛素B在玻璃化之前的治疗效果; (iv)染色质和纺锤体的组织; (v)体外成熟后玻璃化卵母细胞的成熟促进因子(MPF)和有丝分裂原激活的蛋白激酶(MAPK)活性。在有(COC)或无积云细胞(DOs)的体外成熟过程中(0、2和6 h),绵羊卵母细胞在不同的时间进行玻璃化。升温和体外成熟后,与其他组相比,在0 h培养时剥去的卵母细胞显示出更高的存活率和减数分裂成熟率。 Hoechst 33342 /碘化丙啶对COC的双重染色和荧光素黄的显微注射显示玻璃化后广泛的卵丘细胞膜损伤和卵母细胞-卵丘细胞通讯减少。在玻璃化之前用细胞松弛素B处理COC对卵母细胞存活产生负面影响。体外成熟后,纺锤体和染色质构型异常的玻璃化卵母细胞的数量明显高于对照组卵母细胞,而与卵丘细胞无关。去除卵丘细胞结合玻璃化显着降低了MPF和MAPK水平。这项研究提供的证据表明,在玻璃化之前去除卵丘细胞可提高卵母细胞的存活率和减数分裂能力,同时损害可能影响卵母细胞发育能力的重要蛋白质的活性。

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