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γ-干扰素对维甲酸或1,25(OH)₂-维生素D₃诱导单核细胞U937细胞中NADPH氧化酶的协同作用。

Cooperative effects of interferon-gamma on the induction of NADPH oxidase by retinoic acid or 1,25(OH)2-vitamin D3 in monocytic U937 cells.

作者信息

Obermeier H, Sellmayer A, Danesch U, Aepfelbacher M

机构信息

Institut für Prophylaxe und Epidemiologie der Kreislaufkrankheiten und Medizinische Klinik, Klinikum Innenstadt, Universität München, Germany.

出版信息

Biochim Biophys Acta. 1995 Oct 19;1269(1):25-31. doi: 10.1016/0167-4889(95)00095-a.

Abstract

The effect of retinoic acid (RA), 1,25-dihydroxyvitamin D3 (1,25-D3) or human recombinant interferon-gamma (IFN-gamma) on the induction of NADPH oxidase was studied in premonocytic U937 cells. Differentiation with the combination of either RA (1 microM) or 1,25-D3 (10 nM) with IFN-gamma (100 IU/ml) induced NADPH oxidase activity as demonstrated by increased superoxide anion (O2-) generation in response to stimulation with phorbol myristate acetate (PMA, 100 nM). Induction of NADPH oxidase activity was preceded by increases in mRNA levels of p47-phox, p67-phox and gp91-phox, which encode three subunits of the enzyme, and immunoblot analysis of the p47-phox and p67-phox proteins revealed that the increases in mRNA levels were equally reflected by increases in protein levels. In contrast, RA, 1,25-D3 or IFN-gamma alone did not induce NADPH oxidase activity which correlated with their failure to increase p67-phox and gp91-phox mRNA levels. The mRNA of p21 rac1, a GTP-binding protein that regulates NADPH oxidase activity in macrophages, was constitutively expressed in undifferentiated cells and was not affected by differentiation. These data indicate that induction of a functional NADPH oxidase in premonocytic U937 cells requires the cooperative actions of IFN-gamma plus RA or 1,25-D3 and is reflected in the increased expression of p67-phox and gp91-phox.

摘要

在早幼单核细胞U937细胞中研究了视黄酸(RA)、1,25 - 二羟基维生素D3(1,25 - D3)或人重组干扰素 - γ(IFN - γ)对NADPH氧化酶诱导的影响。用RA(1μM)或1,25 - D3(10 nM)与IFN - γ(100 IU/ml)联合诱导分化可诱导NADPH氧化酶活性,这可通过佛波酯肉豆蔻酸酯乙酸盐(PMA,100 nM)刺激后超氧阴离子(O2-)生成增加来证明。NADPH氧化酶活性的诱导之前,编码该酶三个亚基的p47 - phox、p67 - phox和gp91 - phox的mRNA水平增加,并且对p47 - phox和p67 - phox蛋白的免疫印迹分析表明,mRNA水平的增加同样反映在蛋白水平的增加上。相比之下,单独的RA、1,25 - D3或IFN - γ不会诱导NADPH氧化酶活性,这与它们未能增加p67 - phox和gp91 - phox的mRNA水平相关。p21 rac1的mRNA,一种调节巨噬细胞中NADPH氧化酶活性的GTP结合蛋白,在未分化细胞中组成性表达且不受分化影响。这些数据表明,在早幼单核细胞U937细胞中诱导功能性NADPH氧化酶需要IFN - γ加RA或1,25 - D3的协同作用,并且反映在p67 - phox和gp91 - phox表达增加上。

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