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首页> 外文期刊>Molecular reproduction and development >Mitochondrial organization in prepubertal goat oocytes during in vitro maturation and fertilization
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Mitochondrial organization in prepubertal goat oocytes during in vitro maturation and fertilization

机译:体外成熟和受精过程中青春期前山羊卵母细胞的线粒体组织

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The aim of this study was to evaluate mitochondrial distribution during in vitro maturation (at 0, 15, 20, and 27 hr of IVM) and fertilization of prepubertal goat oocytes compared to mitochondrial distribution of ovulated and in vitro fertilized oocytes from adult goats. Oocytes from prepubertal goats were recovered from a slaughterhouse and were matured in M199 with hormones and serum for 27 hr. Ovulated oocytes were collected from gonadotrophin-treated Murciana goats. Frozen-thawed spermatozoa were selected by centrifugation in Percoll gradient and were capacitated in DMH with 20% steer serum for 1 hr. Ovulated and IVM-oocytes were inseminated in DMH medium with steer serum and calcium lactate for 20 hr. Oocytes and presumptive zygotes were stained with Mitotraker Green FM and observed under a confocal laser scanning microscope. Ultrastructural morphology of oocytes and presumptive zygotes were analyzed by transmission electron microscopy (TEM). Prepubertal goat oocytes at germinal vesicle stage (GV) presented mitochondria localized in the cortical and perinuclear region. IVM-oocytes at metaphase II presented mitochondria peripheral polarized to the region opposite were the metaphase spindle is positioned and within the polar body. Ovulated oocytes presented peripheral mitochondria distribution and mitochondrial aggregation around the MII spindle. At 20 hr post-insemination, mitochondria were distributed around the two synchronous pronuclei (2PN rpar; in zygotes ovulated oocytes whereas in prepubertal 2PN-zygotes mitochondria presented a peripheral polarized distribution. Images by TEM detected that immature prepubertal goat oocytes that are less electrodense and present fewer cristae than in vitro matured prepubertal goat oocytes; these are characterized by being associated to swollen vesicles. Mol. Reprod. Dev. 73: 617-626, 2006 (c) 2006 Wiley-Liss, Inc.
机译:这项研究的目的是评估与成年山羊排卵和体外受精卵母细胞的线粒体分布相比,体外成熟(IVM在0、15、20和27小时)和青春期前卵母细胞受精过程中的线粒体分布。从屠宰场回收来自青春期前山羊的卵母细胞,并在含有激素和血清的M199中成熟27小时。从促性腺激素处理过的Murciana山羊中收集有卵的卵母细胞。通过在Percoll梯度中离心选择冻融的精子,并在DMH中用20%转向血清将其精化1小时。将排卵的和IVM卵母细胞在带有转向血清和乳酸钙的DMH培养基中授精20小时。卵母细胞和推定的受精卵用Mitotraker Green FM染色,并在共聚焦激光扫描显微镜下观察。通过透射电子显微镜(TEM)分析了卵母细胞和推定受精卵的超微结构形态。青春期前的山羊胚泡处于生小泡期(GV),线粒体位于皮质和核周区域。中期II的IVM卵母细胞呈线粒体外围极化,相对于中期纺锤体位于极体内的相反区域极化。排卵的卵母细胞在MII纺锤体周围呈现外周线粒体分布和线粒体聚集。授精后20小时,线粒体分布在两个同步原核(2PN rpar;合卵子卵母细胞中,而青春期前2PN-合卵子线粒体呈外周极化分布);透射电镜(TEM)检测到未成熟的青春期前山羊卵母细胞具有较少的电极性和Mol.Reprod.Dev.73:617-626,2006(c)2006 Wiley-Liss,Inc。目前比在体外成熟的青春期前的山羊卵母细胞更少的cr;其特征在于与囊泡肿胀有关。

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