Itoh Takehiro, Kacchi Masayuki, Abe Hiroyuki, Sendai Yutaka, Hoshi Hiroyoshi
Research Institute for the Functional Peptides, Yamagata 990-0823, Japan.
Biol Reprod. 2002 Oct;67(4):1099-105. doi: 10.1095/biolreprod67.4.1099.
The objective of this study was to identify factors that would allow the establishment of a serum-free culture system that could support follicular and oocyte growth, antrum formation, and estradiol-17beta (E(2)) production in preantral follicles of bovine ovaries. Large preantral follicles (145-170 micro m in diameter) were microsurgically dissected from ovaries, embedded in 0.15% type I collagen gels, and maintained in a serum-free medium for up to 13 days at 38.5 degrees C in 5% CO(2) in air. This culture environment allowed most preantral follicles to maintain a three-dimensional structure with the presence of a thecal layer and basement membrane surrounding the granulosa cells throughout the entire culture period. The effects of insulin, insulin-like growth factor (IGF)-I, IGF-II, FSH, and LH on preantral follicle growth were investigated in serum-free medium. Follicular diameters were significantly larger in the presence of insulin, IGF-I, IGF-II, or FSH after 13 days in culture. Oocyte diameters were also significantly larger in the presence of all hormones tested. The single addition of insulin, IGF-I, or FSH induced antrum formation between Days 7 and 13 of culture. Insulin progressively induced E(2) secretion by follicles after antrum formation, but IGF-I and FSH had no apparent effect. FSH and LH caused an increase in oocyte diameter in the presence of insulin. The addition of three hormones (insulin, FSH, and LH) initiated antrum formation and E(2) production earlier than insulin-containing medium alone. Furthermore, maximal E(2) secretion was maintained steadily between 7 and 13 days in this culture condition. From these results, we have demonstrated that insulin, FSH, and LH play substantial roles in the growth and development of bovine large preantral follicles in a serum-free medium.
本研究的目的是确定能够建立无血清培养体系的因素,该体系可支持牛卵巢腔前卵泡的卵泡和卵母细胞生长、腔形成以及雌二醇-17β(E₂)生成。从卵巢中显微手术分离出直径为145 - 170μm的大型腔前卵泡,将其包埋于0.15%的I型胶原凝胶中,并在无血清培养基中于38.5℃、5%二氧化碳的空气中培养长达13天。这种培养环境使大多数腔前卵泡在整个培养期间都能维持三维结构,颗粒细胞周围存在卵泡膜层和基底膜。在无血清培养基中研究了胰岛素、胰岛素样生长因子(IGF)-I、IGF-II、促卵泡激素(FSH)和促黄体生成素(LH)对腔前卵泡生长的影响。培养13天后,在胰岛素、IGF-I、IGF-II或FSH存在的情况下,卵泡直径显著增大。在所有测试激素存在的情况下,卵母细胞直径也显著增大。单独添加胰岛素、IGF-I或FSH可在培养的第7至13天诱导腔形成。腔形成后,胰岛素逐渐诱导卵泡分泌E₂,但IGF-I和FSH没有明显作用。在胰岛素存在的情况下,FSH和LH使卵母细胞直径增加。添加三种激素(胰岛素、FSH和LH)比单独含胰岛素的培养基更早启动腔形成和E₂生成。此外,在这种培养条件下,最大E₂分泌在7至13天之间稳定维持。从这些结果来看,我们已证明胰岛素、FSH和LH在无血清培养基中对牛大型腔前卵泡的生长和发育起着重要作用。