Shaw J, Meerovitch K, Elliott J F, Bleackley R C, Paetkau V
Department of Biochemistry, University of Alberta, Edmonton, Canada.
Mol Immunol. 1987 May;24(5):409-19. doi: 10.1016/0161-5890(87)90014-9.
The expression of several lymphokine gene is characterized by a common pattern of induction, suppression and superinduction. This pattern was studied at the level of cellular mRNA in the mouse T-lymphoma cell line EL4, the human T-leukemia line Jurkat and in normal human peripheral blood lymphocytes. Lymphokine mRNA was induced by stimulating the cells with the phorbol diester PMA (TPA), with or without T-lymphocyte mitogens. The induction of Interleukin-2, Interferon gamma and the Colony Stimulating Factor for granulocytes and macrophages was suppressed by Cyclosporin A at moderate concns. Furthermore, these mRNAs accumulated to extraordinarily high levels (superinduction) if the protein synthesis inhibitor cycloheximide was added during transcription. Superinduction was not due to an increased rate of transcription. CsA interrupted ongoing transcription of IL2 by a mechanism not dependent on the induction of a new protein. The co-ordinate regulation of these genes strongly suggests that common intracellular signals mediate their expression.
几种淋巴因子基因的表达具有诱导、抑制和超诱导的共同模式。这种模式在小鼠T淋巴瘤细胞系EL4、人T白血病细胞系Jurkat以及正常人外周血淋巴细胞的细胞mRNA水平上进行了研究。通过用佛波酯PMA(TPA)刺激细胞来诱导淋巴因子mRNA,无论有无T淋巴细胞有丝分裂原。在中等浓度下,环孢素A可抑制白细胞介素-2、干扰素γ以及粒细胞和巨噬细胞集落刺激因子的诱导。此外,如果在转录过程中加入蛋白质合成抑制剂环己酰亚胺,这些mRNA会积累到极高水平(超诱导)。超诱导并非由于转录速率增加。环孢素A通过一种不依赖于新蛋白质诱导的机制中断了IL2正在进行的转录。这些基因的协同调节强烈表明,共同的细胞内信号介导它们的表达。