Kabakoff B D, Doyle J W, Kandutsch A A
Jackson Laboratory, Bar Harbor, Maine 04609.
Arch Biochem Biophys. 1990 Feb 1;276(2):382-9. doi: 10.1016/0003-9861(90)90736-i.
Following treatment of Chinese hamster ovary cells with inhibitors of mevalonate biosynthesis in the presence of exogenous cholesterol, the cellular concentration of phosphorylated dolichol and the incorporation of [3H]mannose into dolichol-linked saccharides and N-linked glycoproteins declined coincident with a decline in DNA synthesis. Addition of mevalonate to the culture medium increased rates of mannose incorporation into lipid-linked saccharides and restored mannose incorporation into N-linked glycoproteins to control levels within 4 h. After an additional 4 h, synchronized DNA synthesis began. Inhibition of the synthesis of lipid-linked oligosaccharides and N-linked glycoproteins by tunicamycin prevented the induction of DNA synthesis by mevalonate, indicating that glycoprotein synthesis was required for cell division. The results suggest that the rate of cell culture growth may be influenced by the level of dolichyl phosphate acting to limit the synthesis of N-linked glycoproteins.
在用外源性胆固醇处理中国仓鼠卵巢细胞时,若同时添加甲羟戊酸生物合成抑制剂,磷酸化多萜醇的细胞浓度以及[3H]甘露糖掺入多萜醇连接的糖类和N-连接糖蛋白的量会随着DNA合成的下降而下降。向培养基中添加甲羟戊酸可提高甘露糖掺入脂质连接糖类的速率,并在4小时内将甘露糖掺入N-连接糖蛋白的量恢复到对照水平。再过4小时后,同步的DNA合成开始。衣霉素抑制脂质连接寡糖和N-连接糖蛋白的合成可阻止甲羟戊酸诱导的DNA合成,这表明糖蛋白合成是细胞分裂所必需的。结果表明,细胞培养生长速率可能受磷酸多萜醇水平的影响,磷酸多萜醇水平限制了N-连接糖蛋白的合成。