Centre for Integrative Physiology, University of Edinburgh, Hugh Robson Building, George Square, Edinburgh EH8 9XD, UK.
Reproduction. 2010 Jun;139(6):971-8. doi: 10.1530/REP-10-0025. Epub 2010 Mar 5.
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 mum achieved over 15 days in vitro. Further development of this system is needed to support complete oocyte growth and thereafter in vitro maturation.
静息状态的大型哺乳动物卵泡在卵巢皮质培养物中开始生长。能够从早期阶段维持体外发育直到卵母细胞成熟的系统将允许研究调节卵母细胞发育的机制。本研究的目的是 1)确定是否可以从皮质环境中分离出在体外开始生长的牛卵泡,并可以进一步发育,以及 2)评估激活素和 FSH 对来源于原始卵泡的次级卵泡发育的影响。牛卵巢皮质的片段在无血清培养基中培养 6 天;此后,分离次级卵泡进行进一步培养。在总共最多 21 天的体外培养后,将卵泡进行组织学评估或打开以释放卵母细胞-卵丘复合物,通过光学显微镜进行检查。与对照组相比,在激活素暴露的卵泡中观察到卵泡和卵母细胞的显著生长,无论是否存在 FSH,一些卵母细胞直径在 15 天的总体外培养后超过 100 微米。与其他处理组相比,在总共 9 天的体外培养后,在单独培养的激活素中培养的卵泡中观察到显著的雌二醇分泌;然而,这种作用没有持续。总之,本研究证明了在两步无血清培养系统中促进原始牛卵泡的发育,在 15 天的体外培养中可以达到 >100 微米的卵母细胞直径。需要进一步开发该系统以支持完整的卵母细胞生长和随后的体外成熟。