Chiou W J, Bonin P D, Harris P K, Carter D B, Singh J P
Metabolic Diseases Research, Upjohn Company, Kalamazoo, Michigan 49001.
J Biol Chem. 1989 Dec 25;264(36):21442-5.
Our previous studies have demonstrated that platelet-derived growth factor (PDGF) modulated cellular responses to interleukin-1 (IL-1). In this communication, we show that PDGF regulates expression of IL-1 receptor (IL-1 R) gene. Treatment of quiescent cultures of Balb/c 3T3 fibroblasts with PDGF produced 20-30-fold stimulation of IL-1 R mRNA with a concomitant increase in cell surface 125I-binding. IL-1 R mRNA accumulation occurred after an initial lag period and with a time course preceding the increase in 125I-IL-1 binding to cells. Induction of IL-1 R mRNA was blocked by inhibitors of protein synthesis, suggesting that a product of a gene expressed immediately after PDGF addition is required for IL-1 R gene expression. These latter data provide evidence for an ordered sequence of expression of PDGF-inducible "immediate early" gene(s) and IL-1 R gene. These results suggest that in connective tissues, PDGF may be an important determinant in initiating and maintaining cellular responses to IL-1. Such responses may have important consequences in the actions of IL-1 under normal and pathological conditions such as arthritis and atherosclerosis.
我们之前的研究表明,血小板衍生生长因子(PDGF)可调节细胞对白介素-1(IL-1)的反应。在本通讯中,我们表明PDGF可调节IL-1受体(IL-1R)基因的表达。用PDGF处理静止的Balb/c 3T3成纤维细胞培养物,可使IL-1R mRNA受到20 - 30倍的刺激,同时细胞表面125I结合增加。IL-1R mRNA的积累在最初的延迟期后发生,且其时间进程先于125I-IL-1与细胞结合的增加。蛋白质合成抑制剂可阻断IL-1R mRNA的诱导,这表明在添加PDGF后立即表达的基因产物是IL-1R基因表达所必需的。这些数据为PDGF诱导的“立即早期”基因和IL-1R基因的有序表达序列提供了证据。这些结果表明,在结缔组织中,PDGF可能是启动和维持细胞对IL-1反应的重要决定因素。这种反应可能在正常和病理条件下(如关节炎和动脉粥样硬化)IL-1的作用中产生重要影响。