Garber A T, Brasch K
Cytobios. 1982;33(131-32):157-72.
Primary suspension cultures of hepatocytes from adult roosters were prepared by collagenase perfusion. The cells remained viable for better than 12h as assessed by vital dye exclusion, electron microscopy and protein synthesis. In addition to the spectrum of proteins observed in control cultures, hepatocytes from animals pretreated with 17 beta-oestradiol synthesized vitellogenin, low density lipoprotein and several other unidentified peptides. Vg production, as determined by direct immunoprecipitation, was maintained at levels comparable to those observed in vivo with oestrogen treated roosters. Attempts to attain secondary induction of vitellogenesis in vitro, however, using cells from animals in which the primary response had subsided, were not successful. Nonetheless, the results show as a first step, that suspension cultures of liver cells from adult birds can be prepared which remain viable and morphologically differentiated for an extended period.
通过胶原酶灌注制备成年公鸡肝细胞的原代悬浮培养物。通过活体染料排斥、电子显微镜和蛋白质合成评估,细胞存活时间超过12小时。除了在对照培养物中观察到的蛋白质谱外,用17β-雌二醇预处理的动物的肝细胞还合成了卵黄生成素、低密度脂蛋白和其他几种未鉴定的肽。通过直接免疫沉淀测定,卵黄生成素的产生维持在与雌激素处理的公鸡体内观察到的水平相当的水平。然而,使用来自初级反应已经消退的动物的细胞在体外实现卵黄生成的二次诱导的尝试没有成功。尽管如此,结果表明,作为第一步,可以制备成年鸟类肝细胞的悬浮培养物,这些培养物在较长时间内保持存活并在形态上保持分化。