Mackiewicz A, Speroff T, Ganapathi M K, Kushner I
Department of Medicine, Case Western Reserve University, MetroHealth Medical Center, Cleveland, OH 44109.
J Immunol. 1991 May 1;146(9):3032-7.
We evaluated the effects of binary combinations of four cytokines on production of the positive acute phase proteins alpha-1 antichymotrypsin, haptoglobin and fibrinogen, and the negative acute phase proteins albumin and alpha-fetoprotein (AFP) in two human hepatoma cell lines. The effects of the cytokine combinations on the five proteins varied; each protein exhibited a unique and specific pattern of response to the cytokine combinations. In Hep G2 cells, antichymotrypsin was induced by all four cytokines, IL-6, IL-1, TNF-alpha, and transforming growth factor beta 1 alone, and their effects in binary combinations could be attributed to additive or minimally synergistic interactions. Fibrinogen was induced only by IL-6 and this induction was inhibited by IL-1 alpha, TNF-alpha or transforming growth factor beta 1. Haptoglobin was also induced only by IL-6, but TNF-alpha was the only cytokine that inhibited this induction at all concentrations of IL-6. Each of the four cytokines alone down regulated production of AFP and albumin. However, binary combinations of the four cytokines were simply additive, for the most part, in inhibiting AFP production, whereas the inhibitory effects of combinations of cytokines on albumin production differed significantly from simple additive effects. These observations, taken together with studies of effects of cytokine combinations on other acute phase proteins, indicate that the various acute phase proteins respond differently to different combinations of cytokines and that the potential exists for highly specific regulation of synthesis of individual plasma proteins by cytokine interactions. These findings imply that the acute phase response in vivo represents the integrated sum of multiple, separately regulated changes in gene expression.
我们评估了四种细胞因子的二元组合对两种人肝癌细胞系中阳性急性期蛋白α-1抗糜蛋白酶、触珠蛋白和纤维蛋白原,以及阴性急性期蛋白白蛋白和甲胎蛋白(AFP)产生的影响。细胞因子组合对这五种蛋白的影响各不相同;每种蛋白对细胞因子组合都表现出独特且特异的反应模式。在Hep G2细胞中,所有四种细胞因子单独作用时,即白细胞介素-6(IL-6)、白细胞介素-1(IL-1)、肿瘤坏死因子-α(TNF-α)和转化生长因子β1(TGF-β1),均可诱导抗糜蛋白酶的产生,它们二元组合的作用可归因于相加或最小程度的协同相互作用。纤维蛋白原仅由IL-6诱导产生,而IL-1α、TNF-α或TGF-β1可抑制这种诱导作用。触珠蛋白也仅由IL-6诱导产生,但TNF-α是在所有IL-6浓度下唯一能抑制这种诱导作用的细胞因子。四种细胞因子单独作用时均可下调AFP和白蛋白的产生。然而,四种细胞因子的二元组合在抑制AFP产生方面大多只是简单相加,而细胞因子组合对白蛋白产生的抑制作用与简单相加作用有显著差异。这些观察结果,连同细胞因子组合对其他急性期蛋白影响的研究表明,各种急性期蛋白对不同细胞因子组合的反应不同,并且细胞因子相互作用对个体血浆蛋白合成具有高度特异性调节的潜力。这些发现意味着体内急性期反应代表了基因表达中多个单独调节变化的综合总和。