Smith R G, Syms A J, Norris J S
J Steroid Biochem. 1984 Jan;20(1):277-81. doi: 10.1016/0022-4731(84)90217-6.
This report describes androgen induced up-regulation of intracellular androgen receptor concentrations in the DDT1MF-2 cell line derived from the hamster ductus deferens and the R3327H-G8-A1 line derived from the Dunning prostate adenocarcinoma. Within 6 h of exposure to androgens the receptor concentration is increased approximately 2-fold. Incorporation of dense amino-acids and subsequent analysis by sucrose density gradient centrifugation indicates that the observed increase in receptors is possibly due to de novo androgen receptor synthesis. In both cell lines this increase is inhibited by 30-50% within 6 h and completely during a subsequent 18 h period by the potent glucocorticoid triamcinolone acetonide (TA). TA also inhibits the growth of both cell lines and antagonizes the stimulatory effect of androgens. Flow cell cytometry studies indicate that TA blocks the cells in the G1 phase of the cell cycle. This event may be associated with regulation of androgen receptor concentrations.
本报告描述了雄激素诱导源自仓鼠输精管的DDT1MF - 2细胞系和源自邓宁前列腺腺癌的R3327H - G8 - A1细胞系中细胞内雄激素受体浓度上调的情况。在暴露于雄激素6小时内,受体浓度增加约2倍。掺入重氨基酸并随后通过蔗糖密度梯度离心分析表明,观察到的受体增加可能是由于雄激素受体的从头合成。在这两种细胞系中,这种增加在6小时内被抑制30 - 50%,并在随后的18小时内被强效糖皮质激素曲安奈德(TA)完全抑制。TA还抑制这两种细胞系的生长,并拮抗雄激素的刺激作用。流式细胞术研究表明,TA将细胞阻滞在细胞周期的G1期。这一事件可能与雄激素受体浓度的调节有关。