Ge R S, Hardy D O, Catterall J F, Hardy M P
The Population Council and Rockefeller University, New York, New York 10021, USA.
Biol Reprod. 1999 Apr;60(4):855-60. doi: 10.1095/biolreprod60.4.855.
The enzyme 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD) has an important role in androgen metabolism, catalyzing the interconversion of dihydrotestosterone (DHT) and 5alpha-androstane-3alpha,17beta-diol (3alpha-DIOL). The net direction of this interconversion will affect the amount of biologically active ligand available for androgen receptor binding. We hypothesize that in Leydig cells, differential expression of 3alpha-HSD enzymes favoring one of the two directions is a mechanism by which DHT levels are controlled. In order to characterize 3alpha-HSD in rat Leydig cells, the following properties were analyzed: rates of oxidation (3alpha-DIOL to DHT) and reduction (DHT to 3alpha-DIOL) and preference for the cofactors NADP(H) and NAD(H) (i.e., the oxidized and reduced forms of both pyridine nucleotides) in Leydig cells isolated on Days 21, 35, and 90 postpartum. Levels of 3alpha-HSD protein were measured by immunoblotting using an antibody directed against the liver type of the enzyme. Levels of 3alpha-HSD protein and rates of reduction were highest on Day 21 and lowest on Day 90. The opposite was true for the rate of 3alpha-HSD oxidation, which was barely detectable on Day 21 and highest on Day 90 (59.08 +/- 6.35 pmol/min per 10(6) cells, mean +/- SE). Therefore, the level of 3alpha-HSD protein detectable by liver enzyme was consistent with reduction but not with oxidation. There was a clear partitioning of NADP(H)-dependent activity into the cytosolic fraction of Leydig cells, whereas on Days 35 and 90, Leydig cells also contained a microsomal NAD(H)-activated 3alpha-HSD. We conclude that 1) the cytosolic 3alpha-HSD in Leydig cells on Day 21 behaves as a unidirectional NADPH-dependent reductase; 2) by Day 35, a microsomal NAD(H)-dependent enzyme activity is present and may account for predominance of 3alpha-HSD oxidation over reduction and the resultant high capacity of Leydig cells on Day 90 to synthesize DHT from 3alpha-DIOL.
3α-羟基类固醇脱氢酶(3α-HSD)在雄激素代谢中发挥着重要作用,催化双氢睾酮(DHT)与5α-雄甾烷-3α,17β-二醇(3α-DIOL)之间的相互转化。这种相互转化的净方向会影响可用于雄激素受体结合的生物活性配体的量。我们推测,在睾丸间质细胞中,3α-HSD酶偏向两个方向之一的差异表达是控制DHT水平的一种机制。为了表征大鼠睾丸间质细胞中的3α-HSD,我们分析了以下特性:产后第21天、35天和90天分离的睾丸间质细胞中的氧化速率(3α-DIOL转化为DHT)和还原速率(DHT转化为3α-DIOL),以及对辅因子NADP(H)和NAD(H)(即两种吡啶核苷酸的氧化型和还原型)的偏好。使用针对该酶肝脏类型的抗体通过免疫印迹法测量3α-HSD蛋白水平。3α-HSD蛋白水平和还原速率在第21天最高,在第90天最低。3α-HSD氧化速率则相反,在第21天几乎检测不到,在第90天最高(59.08±6.35 pmol/分钟/10(6)个细胞,平均值±标准误)。因此,通过肝脏酶检测到的3α-HSD蛋白水平与还原一致,但与氧化不一致。NADP(H)依赖性活性明显分布在睾丸间质细胞的胞质部分,而在第35天和第90天,睾丸间质细胞还含有微粒体NAD(H)激活的3α-HSD。我们得出结论:1)第21天睾丸间质细胞中的胞质3α-HSD表现为单向NADPH依赖性还原酶;2)到第35天,存在微粒体NAD(H)依赖性酶活性,这可能解释了第90天3α-HSD氧化相对于还原的优势以及睾丸间质细胞从3α-DIOL合成DHT的高能力。