Salomon D S, Vistica D T
Mol Cell Endocrinol. 1979 Jan;13(1):55-71. doi: 10.1016/0303-7207(79)90076-5.
Murine L1210 leukemia cells were cultured in the presence of various steroid hormones to determine their growth response. Cells maintained in medium containing glucocorticoids such as dexamethasone exhibit a 10--20% inhibition of growth, whereas progesterone of 17 beta estradiol produce a 40--50% inhibition of growth. The response is due to growth inhibition and not to any cytolytic effect of the steroids. L1210 cytoplasmic and nuclear extracts contain high affinity binding sites for [3H]dexamethasone, [3H]progesterone and [3H]17 beta-estradiol. Competition with various steroids indicate that estrogens bind to one class of cytoplasmic binding sites, while glucocorticoids and progestins bind to a second class of receptor sites. These receptors appear not be be completely responsible for growth inhibition since there is no correlation between the magnitude of growth inhibition and the intracellular concentration of receptor sites, and since the concentration of steroid required to cause significant growth inhibition exceeds those concentrations required to saturate the cytoplasmic receptors.
将小鼠L1210白血病细胞在各种类固醇激素存在的情况下进行培养,以确定它们的生长反应。维持在含有糖皮质激素(如地塞米松)的培养基中的细胞生长受到10%-20%的抑制,而孕酮或17β-雌二醇则使生长受到40%-50%的抑制。这种反应是由于生长抑制,而非类固醇的任何细胞溶解作用。L1210细胞质和细胞核提取物含有与[3H]地塞米松、[3H]孕酮和[3H]17β-雌二醇的高亲和力结合位点。与各种类固醇的竞争表明,雌激素与一类细胞质结合位点结合,而糖皮质激素和孕激素与另一类受体位点结合。这些受体似乎并非完全导致生长抑制,因为生长抑制的程度与细胞内受体位点的浓度之间没有相关性,而且导致显著生长抑制所需的类固醇浓度超过了使细胞质受体饱和所需的浓度。