Li X, Peegel H, Menon K M
Departments of Obstetrics and Gynecology and Biological Chemistry, University of Michigan, Ann Arbor, Michigan 48109, USA.
Endocrinology. 2001 Jan;142(1):174-81. doi: 10.1210/endo.142.1.7865.
The synthesis of androgens by theca-interstitial cells is stimulated by LH and the insulin/insulin-like growth factor I (IGF-I) system. An essential element of the steroidogenesis is the uptake of plasma cholesterol and transformation to steroid hormones. In the rat, the uptake of cholesterol by the theca-interstitial cells is mediated by the high density lipoprotein receptor. The goal of the present study was to examine whether insulin has any effect on cholesterol delivery into theca-interstitial cells. The effects of insulin and hCG on the expression of the high density lipoprotein receptor (SR-BI) messenger RNA (mRNA) and intracellular cholesterol levels were examined in rat theca-interstitial cells under in vivo and in vitro conditions. Twenty-five-day-old rats were treated with insulin, hCG, or insulin followed by hCG. The expression of SR-BI mRNA was then examined in ovaries enriched in theca-interstitial cell population by Northern blot analysis. Treatment with insulin increased the expression of SR-BI mRNA over that in controls treated with saline. hCG administration also increased the expression of SR-BI mRNA. A combination of insulin followed by hCG produced an even greater increase in SR-BI mRNA expression. Measurements of cellular cholesterol in the ovarian tissue showed an increase in total and free cholesterol levels in response to insulin treatment. As expected, administration of hCG produced a depletion of cellular cholesterol, and the depletion was even more pronounced in response to treatment with insulin and hCG. The effect of insulin and hCG on SR-SBI mRNA expression was then examined under in vitro conditions using primary cultures of theca-interstitial cells. Treatment with insulin produced an increase in SR-BI mRNA expression. As the cultured theca-interstitial cells were not able to maintain hCG receptors, hCG addition produced no increase in SR-BI mRNA expression. However, in the presence of insulin, these cells were able to maintain hCG receptors and readily responded to hCG to increase SR-BI mRNA expression. Although insulin alone produced a modest increase in total and free cholesterol levels, in the presence of insulin, hCG produced the expected depletion of cellular cholesterol content. The present study shows that insulin has a stimulatory effect on the expression of high density lipoprotein receptors in theca-interstitial cells, suggesting that one of the actions of insulin is to increase intracellular cholesterol, which is subsequently mobilized for androgen biosynthesis in theca-interstitial cells.
卵泡膜间质细胞合成雄激素受促黄体生成素(LH)以及胰岛素/胰岛素样生长因子I(IGF-I)系统的刺激。类固醇生成的一个关键要素是血浆胆固醇的摄取并转化为类固醇激素。在大鼠中,卵泡膜间质细胞摄取胆固醇是由高密度脂蛋白受体介导的。本研究的目的是检测胰岛素是否对胆固醇转运至卵泡膜间质细胞有任何影响。在体内和体外条件下,检测了胰岛素和人绒毛膜促性腺激素(hCG)对大鼠卵泡膜间质细胞中高密度脂蛋白受体(SR-BI)信使核糖核酸(mRNA)表达及细胞内胆固醇水平的影响。对25日龄大鼠给予胰岛素、hCG或先给予胰岛素后给予hCG进行处理。然后通过Northern印迹分析检测富含卵泡膜间质细胞群体的卵巢中SR-BI mRNA的表达。与给予生理盐水处理的对照组相比,胰岛素处理增加了SR-BI mRNA的表达。给予hCG也增加了SR-BI mRNA的表达。先给予胰岛素后给予hCG的联合处理使SR-BI mRNA表达增加得更多。对卵巢组织中细胞胆固醇的测量显示,胰岛素处理后总胆固醇和游离胆固醇水平升高。正如预期的那样,给予hCG导致细胞胆固醇耗竭,而在胰岛素和hCG联合处理后这种耗竭更为明显。然后在体外条件下,使用卵泡膜间质细胞原代培养物检测胰岛素和hCG对SR-SBI mRNA表达的影响。胰岛素处理使SR-BI mRNA表达增加。由于培养的卵泡膜间质细胞无法维持hCG受体,添加hCG并未使SR-BI mRNA表达增加。然而,在有胰岛素存在的情况下,这些细胞能够维持hCG受体,并对hCG做出反应,从而增加SR-BI mRNA表达。虽然单独胰岛素使总胆固醇和游离胆固醇水平有适度升高,但在有胰岛素存在的情况下,hCG使细胞胆固醇含量出现预期的耗竭。本研究表明,胰岛素对卵泡膜间质细胞中高密度脂蛋白受体的表达有刺激作用,这表明胰岛素的作用之一是增加细胞内胆固醇,随后这些胆固醇被转运用于卵泡膜间质细胞中的雄激素生物合成。