Beuscher H U, Fallon R J, Colten H R
J Immunol. 1987 Sep 15;139(6):1896-901.
To assess the potential role of membrane interleukin 1 (mIL-1) in modulating expression of acute phase proteins, we studied the effect of fixed mouse peritoneal macrophages and isolated cell membranes on the synthesis of C3 and albumin in human hepatoma Hep 3B cells. An increase in C3 synthesis and decrease in albumin synthesis were detected after incubation of Hep 3B cells with fixed stimulated macrophages or with membrane preparations. Estimates of hepatocellular C3 and albumin mRNA indicated that the mIL-1 regulation was exerted at a pretranslational level. The changes in C3 and albumin expression induced by mIL-1 were inhibited by addition of anti-interleukin 1 (IL-1) antiserum to the macrophages, supporting the hypothesis that a form of IL-1 is present on the outer cell membrane of macrophages. Moreover, cell-surface iodination of macrophages allowed the detection of a 33-kDa IL-1 molecule, suggesting that an IL-1 species, similar to the intracellular precursor of IL-1 is present at the outer cell surface of macrophages. The expression of mIL-1 was temporally dissociated from IL-1 release, indicating that the cell-surface associated IL-1 activity is not the result of adsorbed soluble IL-1. These studies provide a basis for further investigation of the role of mIL-1 in modulating monocytes and macrophages function via cell-cell interactions.
为了评估膜白细胞介素1(mIL-1)在调节急性期蛋白表达中的潜在作用,我们研究了固定的小鼠腹腔巨噬细胞和分离的细胞膜对人肝癌Hep 3B细胞中C3和白蛋白合成的影响。用固定的刺激巨噬细胞或膜制剂孵育Hep 3B细胞后,检测到C3合成增加和白蛋白合成减少。肝细胞C3和白蛋白mRNA的估计表明,mIL-1调节作用于翻译前水平。向巨噬细胞中添加抗白细胞介素1(IL-1)抗血清可抑制mIL-1诱导的C3和白蛋白表达变化,这支持了巨噬细胞外细胞膜上存在一种形式的IL-1的假说。此外,巨噬细胞的细胞表面碘化可检测到一种33 kDa的IL-1分子,这表明在巨噬细胞外细胞表面存在一种类似于IL-1细胞内前体的IL-1种类。mIL-1的表达在时间上与IL-1释放分离,表明细胞表面相关的IL-1活性不是吸附的可溶性IL-1的结果。这些研究为进一步研究mIL-1通过细胞间相互作用调节单核细胞和巨噬细胞功能的作用提供了基础。