Watanabe T, Oishi M
Institute of Applied Microbiology, University of Tokyo, Japan.
Cell Growth Differ. 1992 Dec;3(12):865-71.
Our previous cell fusion experiments have suggested that the in vitro erythroid differentiation of mouse erythroleukemia cells is the result of a synergistic reaction involving two intracellular differentiation-inducing factors (DIF); these were subsequently demonstrated in the cytoplasmic fraction of mouse erythroleukemia cells. Here, we present experimental evidence indicating that, under conditions in which the two factors (DIF-I and DIF-II) are coinduced, a new factor, which can trigger erythroid differentiation upon introduction into undifferentiated mouse erythroleukemia cells, is produced in the cells. A similar factor was also generated in vitro after the incubation of partially purified DIF-I and DIF-II. We found that protein phosphatases could substitute for DIF-II. These and other experiments suggest that protein dephosphorylation at a tyrosine residue(s) is involved in the generation of the new factor.
我们之前的细胞融合实验表明,小鼠红白血病细胞的体外红系分化是涉及两种细胞内分化诱导因子(DIF)的协同反应的结果;随后在小鼠红白血病细胞的细胞质部分证实了这两种因子。在此,我们提供实验证据表明,在两种因子(DIF-I和DIF-II)共同诱导的条件下,细胞中会产生一种新因子,将其导入未分化的小鼠红白血病细胞后可触发红系分化。部分纯化的DIF-I和DIF-II孵育后在体外也产生了类似因子。我们发现蛋白磷酸酶可以替代DIF-II。这些及其他实验表明,酪氨酸残基处的蛋白质去磷酸化参与了新因子的产生。