Lim K, Yoon S J, Lee M S, Byun S H, Kweon G R, Kwak S T, Hwang B D
Department of Biochemistry, School of Medicine, Chungnam National University, Daejeon, Korea.
Biochem Biophys Res Commun. 1996 Jan 17;218(2):490-4. doi: 10.1006/bbrc.1996.0087.
Glucocorticoids are known to inhibit testicular function, and its receptor is also localized in the Sertoli cells. To evaluate possible role of glucocorticoid in Sertoli cells, the effects of dexamethasone on the expression of androgen binding protein (ABP) have been investigated in primary Sertoli cell cultures. Dexamethasone increased ABP mRNA levels, with maximal stimulation reached at 36 hr. The induction of ABP mRNA was dependent on the low concentration (10(-8) and 10(-7) M) of dexamethasone but gradually reduced in the cells treated with high concentration (10(-6) and 10(-5) M). Dexamethasone-induced ABP mRNA level was no change in the cells after addition of cycloheximide but almost reduced by actinomycin-D pretreatment. Steady-state levels of ABP mRNA gradually increased in the Sertoli cells prepared from 14- and 21-days of age corresponding to rat puberty, and ABP mRNA was induced by dexamethasone. These results suggest that ABP gene is transcriptionally regulated by dexamethasone in primary Sertoli cell cultures.
已知糖皮质激素会抑制睾丸功能,其受体也定位于支持细胞中。为评估糖皮质激素在支持细胞中的可能作用,已在原代支持细胞培养物中研究了地塞米松对雄激素结合蛋白(ABP)表达的影响。地塞米松可增加ABP mRNA水平,在36小时时达到最大刺激。ABP mRNA的诱导依赖于低浓度(10^(-8)和10^(-7) M)的地塞米松,但在用高浓度(10^(-6)和10^(-5) M)处理的细胞中逐渐降低。添加环己酰亚胺后,地塞米松诱导的ABP mRNA水平在细胞中没有变化,但经放线菌素-D预处理后几乎降低。在对应于大鼠青春期的14天和21天龄制备的支持细胞中,ABP mRNA的稳态水平逐渐增加,并且ABP mRNA被地塞米松诱导。这些结果表明,在原代支持细胞培养物中,ABP基因受地塞米松转录调控。