Leanderson T, Sundström S, Mårtensson I L, Ny T, Lundgren E
EMBO J. 1982;1(12):1505-11. doi: 10.1002/j.1460-2075.1982.tb01347.x.
The effect of interferon (IFN) on protein synthesis was studied in the Burkitt's lymphoma cell line P3HR-1 by [35S]methionine labelling of the cells, followed by two-dimensional gel electrophoresis of cell extracts. De novo synthesis of three proteins (mol. wts. 33 000, 62 000, and 98 000, respectively) and alterations in the rate of synthesis for a small number of additional proteins were observed during the first 12 h of treatment, while the rate of overall protein synthesis was unaffected. Treatment of P3HR-1 cells with 12-O-tetradecanoyl-phorbol-13-acetate (TPA) or hydrocortisone (HC), which induce similar changes in cell cycle distribution as does IFN, did not induce comparable changes in the rates of protein synthesis. Thus, the effects were specific for IFN and not induced by the change in cell cycle distribution per se, i.e., accumulation in G0. Treatment of cells with 2'-5' pA core did not mimic the effect of IFN at the translational level. A substrain of P3HR-1 cells, selected for resistance to the anti-proliferative effect of IFN, lacked six proteins found in the wild-type. The 62 000 mol. wt. protein was induced in this substrain as well as in native P3HR-1 cells on addition of IFN. The resistant substrain still developed an anti-viral effect in response to IFN. Thus, it seems as if the anti-proliferative and anti-viral effects of IFN, at least in some cells are mediated by different intracellular molecular mechanisms.
通过用[35S]甲硫氨酸标记伯基特淋巴瘤细胞系P3HR-1细胞,然后对细胞提取物进行二维凝胶电泳,研究了干扰素(IFN)对蛋白质合成的影响。在处理的前12小时内,观察到三种蛋白质(分子量分别为33000、62000和98000)的从头合成以及少数其他蛋白质合成速率的改变,而总蛋白质合成速率未受影响。用12-O-十四烷酰佛波醇-13-乙酸酯(TPA)或氢化可的松(HC)处理P3HR-1细胞,它们诱导的细胞周期分布变化与IFN相似,但并未诱导蛋白质合成速率发生类似变化。因此,这些效应是IFN特有的,并非由细胞周期分布本身的变化即G0期积累所诱导。用2'-5' pA核心处理细胞在翻译水平上并未模拟IFN的作用。选择的对IFN抗增殖作用具有抗性的P3HR-1细胞亚系缺乏野生型中发现的六种蛋白质。加入IFN后,该亚系以及天然P3HR-1细胞中均诱导出了分子量为62000的蛋白质。抗性亚系对IFN仍产生抗病毒作用。因此,至少在某些细胞中,IFN的抗增殖和抗病毒作用似乎是由不同的细胞内分子机制介导的。