Siggens K W, Wilkinson M F, Boseley P G, Slocombe P M, Cowling G, Morris A G
Biochem Biophys Res Commun. 1984 Feb 29;119(1):157-62. doi: 10.1016/0006-291x(84)91632-2.
Fresh human peripheral blood mononuclear lymphocytes and lymphoblasts that had been grown for a period in T-cell growth-factor containing medium were stimulated with staphylococcal enterotoxin A plus mezerein to produce interferon-gamma (IFN-gamma). Growing lymphoblasts produced peak levels of IFN-gamma much earlier after induction than fresh lymphocytes. Quantitation of the steady-state levels of IFN-gamma mRNA showed these to differ markedly between the two cell types over a period of time post-induction. In fresh lymphocytes the steady-state levels of IFN-gamma mRNA increased to a peak level over a period of 4 days while in growing lymphoblasts the peak level occurred after 8 hours. These differences in IFN-gamma mRNA production were shown to be not the result of gross alteration of RNA metabolism following blast transformation.
新鲜的人外周血单个核淋巴细胞和在含T细胞生长因子的培养基中培养一段时间的淋巴母细胞,用葡萄球菌肠毒素A加狼毒大戟素刺激以产生γ干扰素(IFN-γ)。与新鲜淋巴细胞相比,正在生长的淋巴母细胞在诱导后产生IFN-γ的峰值水平要早得多。对IFN-γ mRNA稳态水平的定量分析表明,在诱导后的一段时间内,这两种细胞类型之间存在明显差异。在新鲜淋巴细胞中,IFN-γ mRNA的稳态水平在4天内升至峰值,而在正在生长的淋巴母细胞中,峰值在8小时后出现。这些IFN-γ mRNA产生的差异并非是原始淋巴细胞转化后RNA代谢发生重大改变的结果。