Singer J W, Adamson J W
Blood. 1976 Dec;48(6):855-64.
Selected androgenic and nonandrogenic steroids enhance in vitro granulocytic and erythroid colony formation by mouse marrow cells, but do so by influencing either different target cells or cells in different states of cell cycle. Etiocholanolone, a naturally occurring nonandrogenic testosterone metabolite, permits cells not in active cycle to respond to colony-stimulating factor or erythropoietin. Fluoxymesterone, a synthetic androgen, appears to enhance colony growth by increasing the responsiveness of target cells to tropic stimuli. The majority of cells responding to this androgen are in active DNA synthesis. Direct comparison, however, of etiocholanolone-dependent erythroid or granulocytic colony-forming cells demonstrates nonidentity of the target cells. Thus colony-forming units responding to different classes of steroids are in different states of cell cycle and are physically separable. The enhancement of the in vitro response of colony-forming cells to regulating hormones by steroids such as etiocholanolane suggests a mechanism by which such agents may be therapeutically effective in certain cases of marrow failure in man.
某些雄激素和非雄激素类固醇可增强小鼠骨髓细胞在体外的粒细胞和红细胞集落形成,但它们是通过影响不同的靶细胞或处于细胞周期不同状态的细胞来实现的。本胆烷醇酮是一种天然存在的非雄激素睾酮代谢产物,它能使不处于活跃周期的细胞对集落刺激因子或促红细胞生成素产生反应。氟甲睾酮是一种合成雄激素,它似乎通过增加靶细胞对促生长刺激的反应性来促进集落生长。大多数对这种雄激素有反应的细胞处于活跃的DNA合成状态。然而,对依赖本胆烷醇酮的红细胞或粒细胞集落形成细胞进行直接比较,结果表明靶细胞并不相同。因此,对不同类类固醇有反应的集落形成单位处于细胞周期的不同状态,并且在物理上是可分离的。本胆烷醇酮等类固醇增强集落形成细胞对调节激素的体外反应,提示了这些药物在某些人类骨髓衰竭病例中可能具有治疗效果的一种机制。