Bristol L A, Smith M R, Bhat N K, Durum S K
Laboratory of Molecular Immunoregulation, Program Resources, Inc., Frederick, MD.
J Immunol. 1991 Mar 1;146(5):1509-15.
IL-1 alpha regulation of ornithine decarboxylase (ODC) was examined in T cells because IL-1 is a costimulus for T cell proliferation and ODC is a critical enzyme in the metabolic events associated with cellular proliferation. In the present study, we demonstrate that IL-1 alpha induces ODC mRNA and ODC enzyme activity in T cells. Unlike many IL-1 actions on T cells, this did not require a costimulus from the TCR, IL-1 alone being sufficient to induce ODC. The mechanism of IL-1 induction of ODC probably operates at several levels, including transcription, mRNA stability, and translation. Previous studies have shown that IL-1 prepares T cells for replication by increasing the production of c-jun, c-fos, c-myc, growth factors, growth factor receptors, and the response to growth factors. From the present study, ODC induction can be added to the list of IL-1-induced replicative machinery in T cells.
由于白细胞介素-1(IL-1)是T细胞增殖的共刺激因子,而鸟氨酸脱羧酶(ODC)是与细胞增殖相关的代谢事件中的关键酶,因此在T细胞中研究了IL-1α对ODC的调节作用。在本研究中,我们证明IL-1α可诱导T细胞中的ODC mRNA和ODC酶活性。与IL-1对T细胞的许多作用不同,这不需要来自TCR的共刺激,仅IL-1就足以诱导ODC。IL-1诱导ODC的机制可能在多个水平上起作用,包括转录、mRNA稳定性和翻译。先前的研究表明,IL-1通过增加c-jun、c-fos、c-myc、生长因子、生长因子受体的产生以及对生长因子的反应,使T细胞为复制做好准备。从本研究来看,ODC诱导可被添加到T细胞中IL-1诱导的复制机制列表中。