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首页> 外文期刊>Reproduction: The official journal of the Society for the Study of Fertility >Oocyte development in bovine primordial follicles is promoted by activin and FSH within a two-step serum-free culture system
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Oocyte development in bovine primordial follicles is promoted by activin and FSH within a two-step serum-free culture system

机译:在两步无血清培养系统中,激活素和FSH促进了牛原始卵泡中的卵母细胞发育

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Quiescent follicles of large mammals initiate growth within cultured pieces of ovarian cortex. Systems capable of sustaining in vitro development from this early stage until oocyte maturation would allow investigation of mechanisms regulating oocyte development in its entirety. The aims of this study were 1) to determine whether bovine follicles initiated to grow in vitro could be isolated from the cortical environment, and could undergo further development and 2) to evaluate the effect of activin and FSH on the development of secondary follicles derived from primordial follicles. Fragments of bovine ovarian cortex were cultured in serum-free medium for 6 days; thereafter, secondary follicles were isolated for further culture. After a maximum total of 21 days in vitro , follicles were either processed for histological assessment or opened to release the oocyte–cumulus complexes for inspection by light microscopy. Compared with control, significant follicle and oocyte growth were observed in activin-exposed follicles, with or without FSH, with some oocyte diameters measuring over 100 microns following a total in vitro period of 15 days. Significant oestradiol secretion was observed in follicles cultured in activin alone after a total of 9 days in vitro compared with other treatment groups; however, this effect was not sustained. In summary, this study demonstrates the promotion of primordial bovine follicle development within a two-step serum-free culture system with oocyte diameters >100?μm achieved over 15 days in vitro . Further development of this system is needed to support complete oocyte growth and thereafter in vitro maturation.
机译:大型哺乳动物的静止卵泡在卵巢皮质的培养物中开始生长。从这个早期阶段到卵母细胞成熟能够维持体外发育的系统将允许研究调节卵母细胞整个发育的机制。这项研究的目的是:1)确定是否可以从皮质环境中分离出开始在体外生长的牛卵泡,并且可以进行进一步的发育; 2)评估激活素和FSH对衍生自次级卵泡的发育的影响原始卵泡。在无血清培养基中培养牛卵巢皮质片段6天;此后,分离次级卵泡用于进一步培养。在最长总共21天的体外培养后,对卵泡进行处理以进行组织学评估,或者将其打开以释放卵母细胞-卵丘复合物,以进行光学显微镜检查。与对照组相比,在有或没有FSH的情况下,在暴露于激活素的卵泡中观察到明显的卵泡和卵母细胞生长,在总体外培养15天后,某些卵母细胞直径超过100微米。与其他治疗组相比,在总共9天的体外单独激活素培养的卵泡中观察到大量雌二醇分泌。但是,这种效果并没有持续。总而言之,这项研究证明了在两步无血清培养系统中,卵母细胞直径> 100?μm可以在15天之内达到促进原始牛卵泡发育的目的。需要对该系统进行进一步开发以支持卵母细胞的完全生长以及随后的体外成熟。

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