Chauhan D, Kharbanda S M, Rubin E, Barut B A, Mohrbacher A, Kufe D W, Anderson K C
Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, MA 02115.
Blood. 1993 Mar 15;81(6):1540-8.
The present studies have examined the effects of mitogens on induction of early response gene expression in normal peripheral blood T and Jurkat cells. Pokeweed mitogen (PWM) or anti-CD3 significantly increases c-jun messenger RNA (mRNA) levels in T cells. This transient PWM-related increase in c-jun transcripts is maximal after 15 to 30 minutes of exposure of T cells to PWM. PWM induces c-jun gene expression in a concentration-dependent manner. Moreover, PWM similarly induces expression of other genes coding for leucine zipper transcription factors, ie, jun-B and c-fos. Nuclear run on assays demonstrate that PWM treatment is associated with an increased rate of c-jun gene transcription. Transient expression assays with c-jun promoter fragments linked to the chloramphenicol acetyltransferase gene suggest that the PWM-induced increase in transcription is mediated by the AP-1 transcription factor complex. Moreover, treatment of T cells with actinomycin D to block further transcription before their culture with PWM suggests that the increase in c-jun gene expression by PWM is also regulated at least in part by a posttranscriptional mechanism. Cycloheximide does not alter c-jun mRNA induction by PWM. Finally, given that PWM induces B-cell differentiation in an interleukin-6 (IL-6)-mediated, T-cell-dependent manner, the relationship of c-jun and IL-6 gene expression in PWM-stimulated T cells was examined. The induction of IL-6 mRNA in T cells stimulated by PWM occurs after maximal induction of c-jun mRNA, at a time when the latter is no longer detectable. These findings suggest that PWM induces c-jun gene expression in T cells by a transcriptional and posttranscriptional mechanism and that AP-1 confers PWM inducibility of this gene. Because the IL-6 promoter has several potential transcriptional control elements, one of which is an AP-1-binding site, future experiments will evaluate the role of c-jun in the regulation of PWM-induced IL-6 synthesis by T cells.
目前的研究已经检测了丝裂原对正常外周血T细胞和Jurkat细胞中早期反应基因表达诱导的影响。商陆丝裂原(PWM)或抗CD3可显著提高T细胞中c-jun信使核糖核酸(mRNA)水平。T细胞暴露于PWM 15至30分钟后,这种与PWM相关的c-jun转录本的短暂增加达到最大值。PWM以浓度依赖的方式诱导c-jun基因表达。此外,PWM同样诱导编码亮氨酸拉链转录因子的其他基因的表达,即jun-B和c-fos。细胞核转录分析表明,PWM处理与c-jun基因转录速率增加有关。用与氯霉素乙酰转移酶基因相连的c-jun启动子片段进行的瞬时表达分析表明,PWM诱导的转录增加是由AP-1转录因子复合物介导的。此外,在用PWM培养T细胞之前,用放线菌素D处理T细胞以阻断进一步转录,这表明PWM诱导的c-jun基因表达至少部分也受转录后机制调节。放线菌酮不会改变PWM对c-jun mRNA的诱导。最后,鉴于PWM以白细胞介素-6(IL-6)介导的、T细胞依赖的方式诱导B细胞分化,研究了PWM刺激的T细胞中c-jun和IL-6基因表达的关系。PWM刺激的T细胞中IL-6 mRNA的诱导发生在c-jun mRNA最大诱导之后,此时后者已无法检测到。这些发现表明,PWM通过转录和转录后机制诱导T细胞中c-jun基因表达,并且AP-1赋予该基因PWM诱导性。由于IL-6启动子有几个潜在的转录控制元件,其中之一是AP-1结合位点,未来的实验将评估c-jun在T细胞调节PWM诱导的IL-6合成中的作用。