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首页> 外文期刊>Reproduction in Domestic Animals >Oocyte holding in the Iberian red deer (Cervus elaphus hispanicus): Effect of initial oocyte quality and epidermal growth factor addition on in vitro maturation
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Oocyte holding in the Iberian red deer (Cervus elaphus hispanicus): Effect of initial oocyte quality and epidermal growth factor addition on in vitro maturation

机译:ocyte持有Iberian Red Deer(Cervus Elaphus Hispanicus):初始卵母细胞质量和表皮生长因子的影响对体外成熟的影响

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Current in vitro embryo production protocols in the Iberian red deer (Cervus elaphus hispanicus) need to be optimized; oocyte harvesting in situ followed by overnight holding could reduce the human effort and shipping costs. In our work, post-mortem ovaries were retrieved, and the oocytes were harvested and allocated to G1 group (good quality) or G2 + G3 group (low quality). The oocytes were separately subjected to immediate in vitro maturation (IVM) or held overnight in a holding medium composed of 40% of TCM 199 with Earle's salts, 40% TCM 199 with Hanks' salts and 20% fetal bovine serum (FBS), at room temperature (16 hr). In vitro maturation was carried out in a basal medium supplemented or not with 50 ng/ml of epidermal growth factor (EGF). Our data showed that addition of EGF to the maturation medium increases the percentage of G1 oocytes reaching metaphase II (3.9% vs. 50%, basal vs. EGF; p &.001) and decreased their degeneration rate (69.9% vs. 22.2%, basal vs. EGF; p &.01) when oocytes were immediately matured. Overnight holding increased the meiotic competence of G1 oocytes (37.5% matured in basal medium) and EGF increased prophase arrest in G2 + G3 oocytes (16.1% vs. 38.8% in germinal vesicle [GV] stage in basal medium vs. EGF added medium; p &.05). Our data demonstrate that oocyte holding can be used in Iberian red deer oocytes. Interestingly, EGF addition increases the oocytes' meiotic competence in immediately matured oocytes but not after oocyte holding depending upon initial oocyte quality.
机译:目前伊比利亚红鹿(Cervus Eleaphus Hispanicus)的体外胚胎生产方案需要优化;卵母细胞收获原位,随后隔夜持有可能会降低人力努力和运输成本。在我们的工作中,检测验尸卵巢,并收获卵母细胞并分配给G1组(质量好的)或G2 + G3组(低质量)。卵母细胞分别进行立即进行体外成熟(IVM)或在由耳尔盐的40%TCM 199组成的保温介质中保持过夜,40%TCM 199与Hanks盐和20%胎牛血清(FBS),在室温(16小时)。体外成熟在补充或不含50ng / ml表皮生长因子(EGF)的基础培养基中进行。我们的数据显示,添加到成熟培养基的EGF增加了G1卵母细胞的百分比(3.9%与50%,基础Vs.EGF; P& LT; .001)并降低了它们的变性率(69.9%VS 。22.2%,基础vs. egf; p& .01)当卵母细胞立即成熟时。过夜持有增加了G1卵母细胞的减数分裂效力(基础培养基成熟的37.5%),EGF增加了G2 + G3卵母细胞的预先预先捕获(在基础培养基中的生发囊泡[GV]阶段16.1%vs.38.8%。 p& .05)。我们的数据表明,卵母细胞持有可用于伊比利亚红鹿卵母细胞。有趣的是,EGF添加增加了卵母细胞的减少能力,立即成熟的卵母细胞,但不根据初始卵母细胞质量持有卵母细胞。

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