Erickson G F, Magoffin D A, Cragun J R, Chang R J
Department of Reproductive Medicine, University of California-San Diego, La Jolla 92093.
J Clin Endocrinol Metab. 1990 Apr;70(4):894-902. doi: 10.1210/jcem-70-4-894.
The objective of this work was to examine the effects of insulin-like growth factors (IGFs) on estradiol (E2) production by granulosa cells obtained from ovaries of patients with polycystic ovary disease (PCO). Granulosa cells, isolated from ovaries of three PCO patients, were cultured in serum-free medium containing either androstenedione alone (10(-7) M) or androstenedione plus graded doses of FSH, IGF-I, IGF-II, and/or insulin. At the end of the culture period (2, 4, or 6 days) E2 levels in the medium were measured by RIA. The results from each patient were similar, and therefore, the data were pooled. In the 6-day time-course experiments, the control (untreated) cells produced relatively high levels of E2 at 2 days; however, none was detected thereafter. Treatment with FSH (30 ng/mL) stimulated E2 production 4-fold at 2 days, but the stimulatory effects of FSH were not sustained during culture. IGF-I at 30 ng/mL mimicked the effects of FSH. Concomitant treatment with FSH and IGF-I caused synergistic increases in E2 production (3-, 13-, and 33-fold at 2, 4, and 6 days, respectively). Dose-response studies revealed that FSH and IGF-I stimulated E2 production in a dose-dependent fashion (ED50 of FSH and IGF-I, were 1.1 +/- 0.3 and 7.6 +/- 7.2 ng/mL, respectively). In the presence of a maximally effective dose of FSH (30 ng/mL), the cells appeared to become more responsive to IGF-I (ED50 of IGF-I plus FSH, 1.09 +/- 0.29 ng/mL); however, this effect was not significant (P = 0.086). In the presence of a maximally effective dose of IGF-I (30 ng/mL), the stimulatory effect of FSH on E2 production was dramatically amplified, but the IGF-I did not significantly (P = 0.85) change the potency of FSH (ED50 of FSH plus IGF-I, 1.07 +/- 2.3 ng/mL). Treatment with IGF-II over the concentration range of 0.1-100 ng/mL had no effect on either control or FSH-stimulated E2 production. Treatment with insulin, either alone or together with FSH, increased the levels of E2, but the insulin effects were seen only at the highest doses tested (0.3-10 micrograms/mL). The results in these in vitro experiments with PCO granulosa cells indicate that 1) physiological concentrations of IGF-I are as effective as FSH in stimulating E2 production; 2) IGF-I and FSH act synergistically to control the level of E2 production; and 3) this synergy was not observed with insulin or IGF-II.
本研究的目的是检测胰岛素样生长因子(IGFs)对从多囊卵巢疾病(PCO)患者卵巢获取的颗粒细胞产生雌二醇(E2)的影响。从三名PCO患者的卵巢中分离出颗粒细胞,在无血清培养基中培养,培养基中单独含有雄烯二酮(10⁻⁷ M)或雄烯二酮加不同剂量的促卵泡激素(FSH)、胰岛素样生长因子-I(IGF-I)、胰岛素样生长因子-II(IGF-II)和/或胰岛素。在培养期结束时(2、4或6天),通过放射免疫分析(RIA)测定培养基中的E2水平。每位患者的结果相似,因此将数据合并。在为期6天的时间进程实验中,对照(未处理)细胞在2天时产生相对较高水平的E2;然而,此后未检测到E2。用FSH(30 ng/mL)处理在2天时刺激E2产生增加4倍,但在培养过程中FSH的刺激作用未持续。30 ng/mL的IGF-I模拟了FSH的作用。FSH和IGF-I联合处理导致E2产生协同增加(在2、4和6天时分别增加3倍、13倍和33倍)。剂量反应研究表明,FSH和IGF-I以剂量依赖性方式刺激E2产生(FSH和IGF-I的半数有效剂量[ED50]分别为1.1±0.3和7.6±7.2 ng/mL)。在存在最大有效剂量的FSH(30 ng/mL)时,细胞似乎对IGF-I更敏感(IGF-I加FSH的ED50为1.09±0.29 ng/mL);然而,这种效应不显著(P = 0.086)。在存在最大有效剂量的IGF-I(30 ng/mL)时,FSH对E2产生的刺激作用显著增强,但IGF-I未显著(P = 0.85)改变FSH的效力(FSH加IGF-I的ED50为1.07±2.3 ng/mL)。在0.1 - 100 ng/mL浓度范围内用IGF-II处理对对照或FSH刺激的E2产生均无影响。单独或与FSH一起用胰岛素处理可增加E2水平,但仅在测试的最高剂量(0.3 - 10 μg/mL)时观察到胰岛素的作用。这些对PCO颗粒细胞的体外实验结果表明:1)生理浓度的IGF-I在刺激E2产生方面与FSH一样有效;2)IGF-I和FSH协同作用以控制E2产生水平;3)胰岛素或IGF-II未观察到这种协同作用。