Imoto M, Taniguchi Y, Fujiwara H, Umezawa K
Department of Applied Chemistry, Faculty of Science and Technology, Keio University, Yokohama, Japan.
Exp Cell Res. 1994 May;212(1):151-4. doi: 10.1006/excr.1994.1129.
Phosphatidylinositol (PI) synthesis was activated in Rous sarcoma virus-infected NIH3T3 or activated erbB2-transformed NIH3T3 cells. The in vitro activity of CDP-DG:inositol transferase prepared from these cells was also higher than that from normal parent NIH3T3 cells, although phospholipase C and PI kinase activities were not significantly different among these cells. A tyrosine kinase inhibitor, erbstatin, inhibited the PI synthesis in cultured cells, suggesting that Src and ErbB2-associated tyrosine kinases are involved in activation of CDP-DG:inositol transferase in these cell lines.
磷脂酰肌醇(PI)合成在劳氏肉瘤病毒感染的NIH3T3细胞或活化的erbB2转化的NIH3T3细胞中被激活。从这些细胞制备的CDP-DG:肌醇转移酶的体外活性也高于正常亲本NIH3T3细胞,尽管这些细胞之间的磷脂酶C和PI激酶活性没有显著差异。酪氨酸激酶抑制剂埃博霉素抑制培养细胞中的PI合成,表明Src和ErbB2相关的酪氨酸激酶参与了这些细胞系中CDP-DG:肌醇转移酶的激活。