Zhao J, Dorland M, Taverne M A, Van Der Weijden G C, Bevers M M, Van Den Hurk R
Department of Farm Animal Health, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
Mol Reprod Dev. 2000 Jan;55(1):65-74. doi: 10.1002/(SICI)1098-2795(200001)55:1<65::AID-MRD9>3.0.CO;2-H.
The present study was designed to determine whether rat pre-antral follicles can grow under in-vitro conditions. Emphasis is on whether follicular interaction is involved in in-vitro follicle culture, and furthermore its role in follicular development has been assessed. Pre-antral follicles were isolated mechanically from 10-day old rat ovaries. They were divided into small (50 microm < diameter < 100 microm) and large (120 microm < diameter < 200 microm) pre-antral follicles and cultured individually or in groups for 6 days in medium with or without fetal calf serum (FCS). Based on morphological criteria, large pre-antral follicles cultured in groups in serum-free medium had significantly higher survival rates than those cultured individually. In the presence of FCS, no significant difference was detected with respect to the survival. However, the large pre-antral follicles cultured in groups had a significantly greater increase in diameter than those cultured individually. Furthermore, follicles cultured in groups in FCS-containing medium exhibited significantly more follicular cell proliferation than those in serum-free medium, based on DNA measurement. The present culture system (with or without FCS) proved to be insufficient for small pre-antral follicles to stimulate growth comparable to that of large pre-antral follicles. The transmission electron microscopical (TEM) study revealed the ultrastructural differences between follicles cultured in FCS-containing and serum-free media. Taken together, the results suggest that interfollicular factors are involved in follicle development in vitro, which especially at the early folliculogenesis stage plays a positive role in terms of follicular growth as well as survival. The present culture model allows further investigation of factors that regulate early folliculogenesis.
本研究旨在确定大鼠窦前卵泡是否能在体外条件下生长。重点在于体外卵泡培养中是否涉及卵泡间相互作用,并且进一步评估了其在卵泡发育中的作用。从10日龄大鼠卵巢中机械分离出窦前卵泡。将它们分为小(直径50微米<直径<100微米)和大(直径120微米<直径<200微米)窦前卵泡,并在含或不含胎牛血清(FCS)的培养基中单独或分组培养6天。根据形态学标准,在无血清培养基中分组培养的大窦前卵泡存活率显著高于单独培养的卵泡。在有FCS存在的情况下,存活率方面未检测到显著差异。然而,分组培养的大窦前卵泡直径增加显著大于单独培养的卵泡。此外,基于DNA测量,在含FCS培养基中分组培养的卵泡比在无血清培养基中的卵泡表现出明显更多的卵泡细胞增殖。目前的培养系统(含或不含FCS)被证明不足以刺激小窦前卵泡生长至与大窦前卵泡相当的程度。透射电子显微镜(TEM)研究揭示了在含FCS和无血清培养基中培养的卵泡之间的超微结构差异。综上所述,结果表明卵泡间因子参与体外卵泡发育,尤其在卵泡发生早期阶段,在卵泡生长及存活方面发挥积极作用。目前的培养模型有助于进一步研究调节早期卵泡发生的因子。