Tsai-Morris C H, Knox G F, Dufau M L
Molecular Endocrinology Section, National Institute of Child Health and Human Development, Bethesda, MD 20892.
J Steroid Biochem. 1988 Mar;29(3):285-91. doi: 10.1016/0022-4731(88)90028-3.
Studies were conducted to define further the development of the gonadotropin induced, E2 mediated steroidogenic lesion (17-alpha-hydroxylase/17,20-desmolase) in fetal Leydig cell cultures. Analysis of dispersed fetal testes purified by centrifugal elutriation demonstrated a group of cells with sedimentation velocity 12 less than to less than 16.8 mm/h.g containing a small population of adult like "transitional" Leydig cells and homogeneous "fetal" Leydig cell population collected at greater than 19.3 mm/h.g. After cells were cultured for 3 days with addition of 1 microgram oLH at 3 day intervals, the transitional cells showed testosterone accumulation comparable to the fetal cells. In contrast, transitional cells had 10-fold higher basal and hCG-stimulated aromatase activity than fetal cells, and a lack of testosterone response to acute (3 h) hCG stimulation. At day 6, transitional cells steroidogenic ability declined markedly. The fetal population maintained in culture with LH additions every 3 days, showed typical immature Leydig cell response, with enhancement of acute testosterone response to hCG at 3 day (1-fold) and at 6 day of culture (5-fold). Higher doses of LH (5 micrograms/day) or daily treatment of 1 microgram to fetal cultures, induced a lesion of 17 alpha-hydroxylase/17,20-desmolase with reduction of enzymatic activities (P less than 0.01) and impaired testosterone production (P less than 0.01) in response to acute hCG stimulation. Also aromatase was stimulated by hCG + 140% and 50% and E2 receptors were increased by 100 and 180% at 3 days and 6 days of cultures with daily or high dose LH addition, findings consistent with the observation of the E2-mediated lesion during LH action. In conclusion, the cultured fetal Leydig cell provides a useful model to elucidate molecular mechanisms involved in the development of gonadotropin-induced estradiol-mediated desensitization. Treatment of fetal Leydig cell cultures with multiple or frequent doses of LH elevate aromatase activity to necessary levels for the induction of desensitization. We have isolated small population of transitional Leydig cells with morphological characteristics of cells found in 15 day post-natal testis but functional capabilities of adult cells. We have also demonstrated the emergence of a functional adult-like population from the fetal Leydig cell.
开展了多项研究,以进一步明确促性腺激素诱导的、由雌二醇介导的胎儿睾丸间质细胞培养物中类固醇生成损伤(17-α-羟化酶/17,20-裂解酶)的发展情况。对通过离心淘析纯化的分散胎儿睾丸进行分析,结果显示沉降速度在12至16.8毫米/小时·克之间的一组细胞包含少量类似成年的“过渡型”睾丸间质细胞,而沉降速度大于19.3毫米/小时·克的细胞群体为均一的“胎儿型”睾丸间质细胞。细胞每隔3天添加1微克促黄体生成素(oLH)培养3天后,过渡型细胞的睾酮积累与胎儿型细胞相当。相比之下,过渡型细胞的基础和人绒毛膜促性腺激素(hCG)刺激的芳香化酶活性比胎儿型细胞高10倍,且对急性(3小时)hCG刺激缺乏睾酮反应。在第6天,过渡型细胞的类固醇生成能力显著下降。每隔3天添加促黄体生成素进行培养的胎儿型细胞群体,表现出典型的未成熟睾丸间质细胞反应,对hCG的急性睾酮反应在培养3天时增强(1倍),在培养6天时增强(5倍)。更高剂量的促黄体生成素(5微克/天)或每天对胎儿培养物给予1微克,会诱导17-α-羟化酶/17,20-裂解酶损伤,导致酶活性降低(P<0.01),且对急性hCG刺激的睾酮生成受损(P<0.01)。此外,在每天或高剂量添加促黄体生成素的培养3天和6天时,芳香化酶分别受到hCG刺激升高140%和50%,雌激素受体分别增加100%和180%,这些结果与促黄体生成素作用期间雌激素介导的损伤观察结果一致。总之,培养的胎儿睾丸间质细胞为阐明促性腺激素诱导的雌二醇介导的脱敏过程中涉及的分子机制提供了一个有用的模型。用多次或频繁剂量的促黄体生成素处理胎儿睾丸间质细胞培养物,可将芳香化酶活性提高到诱导脱敏所需的水平。我们分离出了少量过渡型睾丸间质细胞,其形态特征与出生后15天睾丸中的细胞相似,但具有成年细胞的功能能力。我们还证明了从胎儿睾丸间质细胞中出现了功能性的类似成年细胞群体。