Failly-Crépin C, Martin G R
Cell Differ. 1979 Feb;8(1):61-73. doi: 10.1016/0045-6039(79)90018-6.
Undifferentiated cells of a clonal line of teratocarcinoma can differentiate in vitro into embryoid bodies with morphological and biochemical features of early mouse embryo. During the first step of differentiation protein synthesis has been analysed by 2 dimensional gel electrophoresis. While new proteins are synthesized, the synthesis of others turned off with the appearance of endodermal cells in embryoid bodies. We have compared protein synthesis during teratocarcinoma differentiation and during early mouse embryogenesis at three stages of mouse preimplantation embryo. The results demonstrate that only the late blastocyst protein synthesis pattern shows most of the polypeptides identified in the differentiated protein synthesis pattern of teratocarcinoma. In contrast, protein synthesis during the early stages of mouse embryonic development is very different from protein synthesis in undifferentiated teratocarcinoma.
畸胎瘤克隆系的未分化细胞在体外可分化为具有早期小鼠胚胎形态和生化特征的胚状体。在分化的第一步,通过二维凝胶电泳分析了蛋白质合成。虽然有新蛋白质合成,但随着胚状体中内胚层细胞的出现,其他一些蛋白质的合成停止了。我们比较了畸胎瘤分化过程以及小鼠植入前胚胎三个阶段的早期小鼠胚胎发生过程中的蛋白质合成。结果表明,只有晚期囊胚的蛋白质合成模式显示出在畸胎瘤分化蛋白质合成模式中鉴定出的大多数多肽。相比之下,小鼠胚胎发育早期的蛋白质合成与未分化畸胎瘤中的蛋白质合成非常不同。