Transactivation of interleukin-2 gene via the nuclear proteins from spleen and brain cells.

Biotechnology therapeutics Pub Date : 1993-01-01
T B Kazakova, O I Golovko, G V Gushchin, L V Lebedeva, O D Dolgi, E A Karandaschov, A A Mulberg
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Abstract

Immunomodulatory action of nuclear proteins derived from spleen and brain of immunized rats was found in ConA-stimulated mouse spleen lymphocyte cultures. In vitro experiments on 32P- or Dig-labeled promoter-enhancer region (-548 bp) of the human interleukin-2 (IL-2) gene showed specific DNA-nuclear protein complex formation for spleen (6-14 kD) and brain (21 kD) proteins. The functional influence of these trans-factors on the IL-2 promoter region was studied in the model system of Jurkat cells with the firefly luciferase (Luc) reporter gene. The spleen and brain proteins were shown to influence the membrane surface properties of thymic and spleen cells as revealed in a two-phase aqueous system. We conclude that both spleen and brain from immunized rats contain certain protein trans-factors which can be active in T cells and display a common mode of regulatory action the level of IL-2 gene.

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白细胞介素-2基因通过脾和脑细胞核蛋白的转激活。
在cona刺激的小鼠脾淋巴细胞培养中发现免疫大鼠脾和脑核蛋白的免疫调节作用。在人白细胞介素-2 (IL-2)基因32P或dig标记的启动子增强子区(-548 bp)的体外实验中,发现脾脏(6-14 kD)和脑(21 kD)蛋白形成特异性的dna -核蛋白复合物。在具有萤火虫荧光素酶(Luc)报告基因的Jurkat细胞模型系统中,研究了这些反式因子对IL-2启动子区域的功能影响。脾蛋白和脑蛋白影响胸腺细胞和脾细胞的膜表面特性。我们得出结论,免疫大鼠脾和脑均含有一定的蛋白反式因子,这些蛋白反式因子可在T细胞中活化,并表现出共同的IL-2基因水平调节模式。
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