首页> 外文OA文献 >Meiotic maturation of incompetent prepubertal sheep oocytes is induced by paracrine factor(s) released by gonadotropin-stimulated oocyte-cumulus cell complexes and involves mitogen-activated protein kinase activation.
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Meiotic maturation of incompetent prepubertal sheep oocytes is induced by paracrine factor(s) released by gonadotropin-stimulated oocyte-cumulus cell complexes and involves mitogen-activated protein kinase activation.

机译:促性腺激素刺激的卵母细胞-卵丘细胞复合物释放的旁分泌因子诱导不称职的青春期前绵羊卵母细胞的减数分裂成熟,并涉及促分裂原活化的蛋白激酶激活。

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摘要

In this study, sheep oocyte-cumulus cell complexes (OCC) derived from medium (M) antral follicles (M-OCC) were in vitro matured alone or in coculture with OCC derived from small (S) antral follicles (S-OCC) to investigate the contribution of cumulus cells (CC) and oocytes to the process of oocyte meiotic maturation and cumulus expansion (CE). Experiments were conducted with or without gonadotropins (FSH/LH). Regardless of culture conditions, about 12% of S-oocytes reached the metaphase II stage, and S-CC showed a low degree of CE. In contrast, both maturational processes were significantly stimulated by gonadotropins in M-OCC. However, about 48% of S-oocytes progressed to metaphase II, and S-CC expanded after coculture with gonadotropin-stimulated M-OCC and M-CC but not with mural granulosa cells. Both maturational processes were inhibited when S-OCC were cocultured with M-denuded oocytes, or when S-denuded oocytes were cocultured with M-CC. The capacity of these paracrine factor(s) to activate the MAPK pathway in somatic and germ cells of S-complexes was investigated. It was found that MAPK kinase/MAPK phosphorylation levels in M-OCC but not in S-OCC were significantly increased by gonadotropins, first inCCand later in the oocytes. Kinase phosphorylations were activated only in S-oocytes cocultured with M-OCC or M-CC. These results demonstrate that soluble factors specifically produced by M-CC are capable to induce meiotic maturation and CE in S-complexes by acting via CC. These factors can induce MAPK activation only in S-oocytes, whose meiotic arrest could be due to the inability of surrounding CC to respond to gonadotropin stimulation.[...]
机译:在这项研究中,将源自中等(M)窦卵泡(M-OCC)的绵羊卵母细胞-卵丘细胞复合物(OCC)单独体外培养或与源自较小(S)窦卵泡(S-OCC)的OCC共培养至体外。研究卵丘细胞(CC)和卵母细胞对卵母细胞减数分裂成熟和卵丘扩张(CE)过程的贡献。在有或没有促性腺激素(FSH / LH)的情况下进行实验。无论培养条件如何,约12%的S-卵母细胞达到中期II期,S-CC的CE程度较低。相比之下,M-OCC中的促性腺激素显着刺激了两个成熟过程。然而,约48%的S卵母细胞发展至中期II,与促性腺激素刺激的M-OCC和M-CC共培养后,S-CC扩增,但与壁颗粒细胞无共培养。当S-OCC与M裸露的卵母细胞共培养时,或当S-裸露的卵母细胞与M-CC共培养时,两种成熟过程均受到抑制。研究了这些旁分泌因子激活S复合体的体细胞和生殖细胞中MAPK途径的能力。结果发现,促性腺激素使卵母细胞中的MAPK激酶/ MAPK磷酸化水平显着增加,而S-OCC中的MAPK激酶/ MAPK磷酸化水平却没有增加。激酶磷酸化仅在与M-OCC或M-CC共培养的S卵母细胞中被激活。这些结果表明,由M-CC特异产生的可溶性因子能够通过CC来诱导S复合物中的减数分裂成熟和CE。这些因素只能在S卵母细胞中诱导MAPK活化,其减数分裂阻滞可能是由于周围CC无法对促性腺激素刺激作出反应。[...]

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