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使用非贴壁依赖克隆琼脂试验检测对表皮生长因子(EGF)、成纤维细胞生长因子(FGF)和促性腺激素制剂反应不同的颗粒细胞亚类。

The detection of subclasses of granulosa cells with differing responsiveness to EGF, FGF, and gonadotropin preparations using an anchorage-independent clonal agar assay.

作者信息

Bertoncello I, Bradley T R

出版信息

Int J Cell Cloning. 1984 Jan;2(1):9-19. doi: 10.1002/stem.5530020104.

Abstract

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.

摘要

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。

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