Farrar W L, Evans S W, Rapp U R, Cleveland J L
J Immunol. 1987 Sep 15;139(6):2075-80.
Elevation of intracellular cyclic adenosine 3':5' monophosphate (cAMP) inhibits interleukin 2 (IL-2)-stimulated proliferation of a murine cytotoxic cell clone, CT6. The effects of antiproliferative dosages of stable cAMP-derivative, 8-bromoadenosine 3':5'-monophosphate (8-Br-cAMP), on steady state mRNA expression stimulated by IL-2 was examined. IL-2 stimulated mRNA accumulation of three nuclear proto-oncogenes c-fos, c-myc, and c-myb. 8-Br-cAMP alone stimulated c-fos, c-myb, and IL-2 receptor mRNA accumulation as determined by Northern blot analysis. 8-Br-cAMP, however, markedly inhibited c-myc expression stimulated by IL-2. Furthermore, although c-fos and IL-2 receptor mRNA expression was potentiated by 8-Br-cAMP, suppression of protein synthesis was seen. We show that antiproliferative cAMP stimulates similar mRNA expression as does IL-2, with the exception of c-myc. Although a comparative stimulation of steady state mRNA accumulation of some genes occurs, cAMP may profoundly effect protein synthesis. cAMP, therefore, acts on multiple targets involved in the macromolecular events stimulated by IL-2.
细胞内环磷酸腺苷(cAMP)水平升高会抑制白细胞介素2(IL-2)刺激的小鼠细胞毒性细胞克隆CT6的增殖。研究了稳定的cAMP衍生物8-溴腺苷3':5'-单磷酸(8-Br-cAMP)的抗增殖剂量对IL-2刺激的稳态mRNA表达的影响。IL-2刺激了三种核原癌基因c-fos、c-myc和c-myb的mRNA积累。通过Northern印迹分析确定,单独的8-Br-cAMP刺激了c-fos、c-myb和IL-2受体mRNA的积累。然而,8-Br-cAMP显著抑制了IL-2刺激的c-myc表达。此外,尽管8-Br-cAMP增强了c-fos和IL-2受体mRNA的表达,但仍观察到蛋白质合成受到抑制。我们发现,除了c-myc外,抗增殖的cAMP刺激的mRNA表达与IL-2相似。尽管一些基因的稳态mRNA积累受到了比较性刺激,但cAMP可能会深刻影响蛋白质合成。因此,cAMP作用于参与IL-2刺激的大分子事件的多个靶点。