Muñoz E, Zubiaga A, Olson D, Huber B T
Department of Pathology, Tufts University School of Medicine, Boston, MA 02111.
Proc Natl Acad Sci U S A. 1989 Dec;86(23):9461-4. doi: 10.1073/pnas.86.23.9461.
In this report we present evidence that Con A-activated T helper 2 cells transcribe the interleukin 2 (IL-2) gene when cycloheximide is added 3 hr after stimulation. This IL-2 mRNA can be translated into functional protein. However, no steady-state mRNA for gamma-interferon can be detected under the same experimental conditions. Furthermore, when cycloheximide is administered at time 0 of activation, no IL-2 mRNA is seen. Nuclear run-on experiments indicate that IL-2 transcription in T helper 2 cells depends on the presence of cycloheximide. It is likely, therefore, that activation of T helper 2 cells leads to the production of a labile regulatory protein that represses the expression of the IL-2 gene. These findings provide insight into the molecular mechanism that governs the differentiation of interleukin 4-producing T helper 2 cells from IL-2-producing precursor cells.
在本报告中,我们提供证据表明,在刺激后3小时添加放线菌酮时,刀豆蛋白A激活的辅助性T细胞2会转录白细胞介素2(IL-2)基因。这种IL-2信使核糖核酸(mRNA)能够被翻译成功能性蛋白质。然而,在相同实验条件下无法检测到γ-干扰素的稳态mRNA。此外,在激活时间0给予放线菌酮时,看不到IL-2 mRNA。细胞核连续转录实验表明,辅助性T细胞2中的IL-2转录依赖于放线菌酮的存在。因此,辅助性T细胞2的激活可能导致产生一种不稳定的调节蛋白,该蛋白会抑制IL-2基因的表达。这些发现为控制从产生IL-2的前体细胞分化为产生白细胞介素4的辅助性T细胞2的分子机制提供了见解。