Roy S K, Greenwald G S
Department of Obstetrics & Gynecology, University of Nebraska Medical Center, Omaha 68198.
Biol Reprod. 1991 May;44(5):889-96. doi: 10.1095/biolreprod44.5.889.
Preantral (stages 1-6) and antral (stages 7-10) follicles from proestrous hamsters were exposed for 24 h to 1, 5, 10, 50, and 100 ng/ml of epidermal growth factor (EGF), insulin-like growth factor-I (IGF-I), and fibroblast growth factor (FGF) and 1 microCi [3H]thymidine to determine the rate of DNA replication. FSH (100 ng/ml) was used as a positive control. Synergism was also studied by using suboptimal doses of growth factors (1 ng/ml) and FSH (5 ng/ml). Optimal doses (50 ng/ml) of EGF, IGF-I, and FGF, and 100 ng/ml FSH significantly enhanced follicular DNA replication, whereas suboptimal doses of FSH, EGF, and IGF-I affected only a few preantral stages, and FGF was totally ineffective. FGF significantly inhibited DNA synthesis induced by a suboptimal dose of EGF but did not affect IGF-I-induced DNA replication. Paradoxically, a combination of suboptimal doses of all three growth factors significantly (p less than 0.05) stimulated DNA synthesis for all stages; FSH (5 ng/ml) had no additive effect. FSH significantly stimulated follicular progesterone (P4), androstenedione (A), and estradiol-17 beta (E2) accumulation, but significant P4 accumulation from stages 3-10 was observed only after optimal EGF exposure; A and E2 accumulations were unaffected by any of the growth factors. These results indicate that EGF, IGF-I, and FGF stimulate DNA replication to hamster preantral and antral follicles, and may play roles as intraovarian factors regulating folliculogenesis.(ABSTRACT TRUNCATED AT 250 WORDS)
将动情前期仓鼠的窦前卵泡(1-6期)和窦卵泡(7-10期)暴露于1、5、10、50和100 ng/ml的表皮生长因子(EGF)、胰岛素样生长因子-I(IGF-I)和成纤维细胞生长因子(FGF)以及1微居里[3H]胸腺嘧啶24小时,以确定DNA复制速率。促卵泡激素(FSH,100 ng/ml)用作阳性对照。还通过使用次优剂量的生长因子(1 ng/ml)和FSH(5 ng/ml)研究协同作用。EGF、IGF-I和FGF的最佳剂量(50 ng/ml)以及100 ng/ml FSH显著增强卵泡DNA复制,而FSH、EGF和IGF-I的次优剂量仅影响少数窦前阶段,FGF则完全无效。FGF显著抑制次优剂量EGF诱导的DNA合成,但不影响IGF-I诱导的DNA复制。矛盾的是,所有三种生长因子的次优剂量组合对所有阶段均显著(p<0.05)刺激DNA合成;FSH(5 ng/ml)无相加作用。FSH显著刺激卵泡孕酮(P4)、雄烯二酮(A)和雌二醇-17β(E2)积累,但仅在最佳EGF暴露后才观察到3-10期有显著的P4积累;A和E2积累不受任何生长因子影响。这些结果表明,EGF、IGF-I和FGF刺激仓鼠窦前卵泡和窦卵泡的DNA复制,并可能作为调节卵泡发生的卵巢内因子发挥作用。(摘要截短于250字)