Rengarajan Srinivasan, Balasubramanian Karundevi
Department of Endocrinology, Dr. ALM Post-Graduate Institute of Basic Medical Sciences, University of Madras, Taramani Campus, Chennai 600 113, India.
J Cell Biochem. 2008 Apr 1;103(5):1472-87. doi: 10.1002/jcb.21533.
The present study was designed to investigate the dose-dependent direct effect of corticosterone on adult rat Leydig cell steroidogenesis in vitro. Leydig cells were isolated from the testis of normal adult male albino rats, purified on discontinuous Percoll gradient and plated in culture plates/flasks overnight at 34 degrees C in a CO(2) incubator under 95% air and 5% CO(2) using DME/F12 medium containing 1% fetal bovine serum. After the attachment of cells, serum-containing medium was removed and cells were exposed to different doses (0, 50, 100, 200, 400, and 800 nM) of corticosterone using serum-free fresh medium for 24 h at 34 degrees C. At the end of exposure period, cells were utilized for assessment of the activities and mRNA expression of steroidogenic enzymes (cytochrome P(450) side chain cleavage enzyme, 3beta-hydroxysteroid dehydrogenase, 17beta-hydroxysteroid dehydrogenase, and cytochrome P(450) aromatase) and steroidogenic acute regulatory protein gene expression. Testosterone and estradiol production were also quantified. Activities of cytochrome P(450) side chain cleavage enzyme, 3beta- and 17beta-hydroxysteroid dehydrogenases were declined significantly in a dose-dependent manner after corticosterone exposure, while their mRNA expression were significantly reduced at higher doses of corticosterone exposure. The activity and mRNA expression of cytochrome P(450) aromatase registered a significant increase at 100 nM dose of corticosterone whereas at 200-800 nM doses both the activity as well as the mRNA levels was significantly reduced below the basal level. StAR protein gene expression was significantly inhibited by higher doses of corticosterone employed. At all doses employed, corticosterone significantly reduced the production of testosterone by Leydig cells, while estradiol level registered a significant increase at 50 and 100 nM doses but at higher doses, it registered a significant decrease when compared to basal level. It is concluded from the present in vitro study that the molecular mechanism by which corticosterone reduces the production of Leydig cell testosterone is by reducing the activities and mRNA expression of steroidogenic enzymes and steroidogenic acute regulatory protein.
本研究旨在探讨皮质酮对成年大鼠睾丸间质细胞体外类固醇生成的剂量依赖性直接作用。从正常成年雄性白化大鼠的睾丸中分离出睾丸间质细胞,通过不连续的Percoll梯度进行纯化,并在含有1%胎牛血清的DME/F12培养基中,于34℃、95%空气和5%二氧化碳的二氧化碳培养箱中在培养板/培养瓶中培养过夜。细胞贴壁后,去除含血清的培养基,使用无血清新鲜培养基将细胞暴露于不同剂量(0、50、100、200、400和800 nM)的皮质酮中,在34℃下培养24小时。在暴露期结束时,利用细胞评估类固醇生成酶(细胞色素P450侧链裂解酶、3β-羟基类固醇脱氢酶、17β-羟基类固醇脱氢酶和细胞色素P450芳香化酶)的活性和mRNA表达以及类固醇生成急性调节蛋白基因表达。还对睾酮和雌二醇的产生进行了定量。皮质酮暴露后,细胞色素P450侧链裂解酶、3β-和17β-羟基类固醇脱氢酶的活性以剂量依赖性方式显著下降,而在较高剂量的皮质酮暴露下,它们的mRNA表达显著降低。细胞色素P450芳香化酶的活性和mRNA表达在100 nM剂量的皮质酮时显著增加,而在200 - 800 nM剂量时,活性和mRNA水平均显著降低至基础水平以下。较高剂量的皮质酮显著抑制了类固醇生成急性调节蛋白基因表达。在所使用的所有剂量下,皮质酮均显著降低了睾丸间质细胞睾酮的产生,而雌二醇水平在50和100 nM剂量时显著增加,但在较高剂量时,与基础水平相比显著降低。从目前的体外研究得出结论,皮质酮降低睾丸间质细胞睾酮产生的分子机制是通过降低类固醇生成酶和类固醇生成急性调节蛋白的活性及mRNA表达。