Bertoncello I, Bradley T R
Int J Cell Cloning. 1984 Jan;2(1):9-19. doi: 10.1002/stem.5530020104.
Subpopulations of granulosa cells of differing responsiveness to epidermal growth factor (EGF), fibroblast growth factor (FGF), pituitary gonadotropin preparations, and rat erythrocyte suspensions (RBC) have been detected using an anchorage-independent clonal agar assay. All growth factor preparations were capable of enhancing colony formation when added alone, and elicited cloning efficiencies as high as 35% when added to the culture system at optimal concentrations in a variety of combinations. The FGF preparation was the single most effective stimulator of colony formation, augmenting both colony numbers and colony size at concentrations as low as 50 ng/ml. However, unlike the other growth factors in this assay system, a plateau in responsiveness could not be reached even at levels as high as 1 microgram/ml. NIH-FSH-P2 and NIAMMD-bLH-4 were considerably less potent than other growth factors. Both preparations were inactive at concentrations less than 1 microgram/ml and produced an optimal response at 10 micrograms/ml.
使用非贴壁依赖克隆琼脂试验已检测到对表皮生长因子(EGF)、成纤维细胞生长因子(FGF)、垂体促性腺激素制剂和大鼠红细胞悬液(RBC)反应性不同的颗粒细胞亚群。所有生长因子制剂单独添加时均能增强集落形成,以各种组合在最佳浓度添加到培养系统中时,克隆效率高达35%。FGF制剂是集落形成的最有效单一刺激物,在低至50 ng/ml的浓度下即可增加集落数量和集落大小。然而,与该试验系统中的其他生长因子不同,即使在高达1微克/毫升的水平也无法达到反应平台期。NIH-FSH-P2和NIAMMD-bLH-4的效力远低于其他生长因子。两种制剂在浓度低于1微克/毫升时均无活性,在10微克/毫升时产生最佳反应。