Geiger T, Andus T, Bauer J, Northoff H, Ganter U, Hirano T, Kishimoto T, Heinrich P C
Biochemisches Institut, Freiburg, Federal Republic of Germany.
Eur J Biochem. 1988 Jul 15;175(1):181-6. doi: 10.1111/j.1432-1033.1988.tb14181.x.
Secretory products of cultured human blood monocytes contain a hepatocyte-stimulating factor which is able to induce the acute-phase proteins alpha 2-macroglobulin and fibrinogen in rat liver cells. Total RNA was isolated from unstimulated and lipopolysaccharide-stimulated human monocytes and translated in a reticulocyte lysate. The capability of the cell-free synthesized proteins to induce the acute-phase proteins alpha 2-macroglobulin and fibrinogen was assayed in rat hepatocyte primary cultures and in the rat hepatoma cell line Fao. The products translated from the mRNA of lipopolysaccharide-stimulated human monocytes induced mRNAs for alpha 2-macroglobulin and fibrinogen and therefore contain hepatocyte-stimulating factor. The translation products of unstimulated monocytes had no effect. A cDNA containing the coding sequence for interleukin-6 (B-cell stimulatory factor 2, interferon-beta 2/26-kDa protein, interleukin HP1) derived from human T-cells cloned into the transcription vector pGEM4 was transcribed in vitro. Translation of the isolated RNA in a reticulocyte lysate led to the synthesis of a protein of about 25 kDa. This cell-free synthesized interleukin-6 exhibited hepatocyte-stimulating activity measured by the induction of beta-fibrinogen mRNA in Fao cells. Using an antibody against interleukin-6, two proteins of 22 kDa and 23 kDa were immunoprecipitated from the culture medium of lipopolysaccharide-stimulated human monocytes. These two proteins were not synthesized by unstimulated monocytes. When total RNA from unstimulated human monocytes and lipopolysaccharide-stimulated human monocytes and lymphocytes was subjected to Northern analysis and hybridized with the interleukin-6 cDNA, a strong hybridization signal corresponding to an RNA of about 1300 bases was detected only in the RNA from lipopolysaccharide-stimulated human monocytes, indicating that human monocytes express the interleukin-6 gene after stimulation. The data presented in this paper strongly suggest that hepatocyte-stimulating factor from human monocytes and interleukin-6 from T-cells are identical.
培养的人血单核细胞的分泌产物含有一种肝细胞刺激因子,该因子能够在大鼠肝细胞中诱导急性期蛋白α2-巨球蛋白和纤维蛋白原。从未受刺激和经脂多糖刺激的人单核细胞中分离出总RNA,并在网织红细胞裂解物中进行翻译。在大鼠肝细胞原代培养物和大鼠肝癌细胞系Fao中测定无细胞合成蛋白诱导急性期蛋白α2-巨球蛋白和纤维蛋白原的能力。从经脂多糖刺激的人单核细胞的mRNA翻译而来的产物诱导了α2-巨球蛋白和纤维蛋白原的mRNA,因此含有肝细胞刺激因子。未受刺激的单核细胞的翻译产物没有作用。将源自人T细胞的含有白细胞介素-6(B细胞刺激因子2、干扰素-β2/26 kDa蛋白、白细胞介素HP1)编码序列的cDNA克隆到转录载体pGEM4中,进行体外转录。在网织红细胞裂解物中对分离的RNA进行翻译,导致合成了一种约25 kDa的蛋白质。这种无细胞合成的白细胞介素-6通过在Fao细胞中诱导β-纤维蛋白原mRNA来测定,表现出肝细胞刺激活性。使用抗白细胞介素-6抗体,从经脂多糖刺激的人单核细胞的培养基中免疫沉淀出两种分别为22 kDa和23 kDa的蛋白质。这两种蛋白质不是由未受刺激的单核细胞合成的。当从未受刺激的人单核细胞、经脂多糖刺激的人单核细胞和淋巴细胞中提取的总RNA进行Northern分析,并与白细胞介素-6 cDNA杂交时,仅在经脂多糖刺激的人单核细胞的RNA中检测到对应于约1300个碱基的RNA的强杂交信号,表明人单核细胞在刺激后表达白细胞介素-6基因。本文提供的数据有力地表明,人单核细胞的肝细胞刺激因子和T细胞的白细胞介素-6是相同的。