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多聚核糖核苷酸激活巨噬细胞过程中基因表达的差异调节。内源性干扰素的作用。

Differential regulation of gene expression during macrophage activation with a polyribonucleotide. The role of endogenously derived IFN.

作者信息

Riches D W, Henson P M, Remigio L K, Catterall J F, Strunk R C

机构信息

Department of Pediatrics, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.

出版信息

J Immunol. 1988 Jul 1;141(1):180-8.

PMID:3379303
Abstract

The activation of macrophages by exposure to the polyribonucleotide, poly [I:C], is accompanied by a large stimulation of the synthesis of the C components factor B and C3, and a concomitant inhibition of the synthesis of the lysosomal enzyme beta-glucuronidase. Northern blot analysis of poly [A+] RNA extracted from poly [I:C]-stimulated cells revealed that the changes in the synthesis of factor B and C3 were related to changes in the levels of their respective mRNA and hence the expression of these proteins appeared to be regulated at a pre-translational level. The down-regulation of the synthesis of beta-glucuronidase appeared to be regulated at both translational and pre-translational levels. In view of the proposed role of macrophage-derived IFN in the regulation of macrophage activation, we investigated the possible role of IFN-alpha/beta in the regulation of the synthesis of factor B, C3, and beta-glucuronidase. Exposure of macrophages to mouse IFN-alpha and IFN-beta induced limited changes in the synthesis of factor B, C3, and beta-glucuronidase. However, pretreatment of macrophages with only 500 U/ml of IFN-beta primed the cells thereby increasing their sensitivity to poly [I:C]. IFN-alpha was less effective as a priming agent. When macrophages were exposed to poly [I:C] in the presence of an anti-mouse IFN-alpha/beta antiserum, the changes in the synthesis of factor B, C3, and beta-glucuronidase were partially inhibited. Collectively, these data indicate first, that exposure of mouse bone marrow-derived macrophages to poly [I:C] differentially regulates the expression of the products of the genes for factor B, C3, and beta-glucuronidase. Second, IFN-alpha and IFN-beta prime macrophages to increase the sensitivity of macrophages to poly [I:C]. Third, in the absence of exogenous IFN, macrophage-derived IFN appears to participate in priming the cells in an autocrine or paracrine fashion.

摘要

通过暴露于多聚核糖核苷酸聚肌苷酸-聚胞苷酸(poly [I:C])激活巨噬细胞,伴随着补体成分B因子和C3合成的大幅增加,以及溶酶体酶β-葡萄糖醛酸酶合成的同时抑制。对从poly [I:C]刺激的细胞中提取的聚腺苷酸加尾RNA(poly [A+] RNA)进行Northern印迹分析表明,B因子和C3合成的变化与它们各自mRNA水平的变化相关,因此这些蛋白质的表达似乎在翻译前水平受到调节。β-葡萄糖醛酸酶合成的下调似乎在翻译和翻译前水平均受到调节。鉴于巨噬细胞衍生的干扰素在巨噬细胞激活调节中的假定作用,我们研究了干扰素α/β在调节B因子、C3和β-葡萄糖醛酸酶合成中的可能作用。将巨噬细胞暴露于小鼠干扰素α和干扰素β会导致B因子、C3和β-葡萄糖醛酸酶合成的有限变化。然而,仅用500 U/ml的干扰素β预处理巨噬细胞会使细胞致敏,从而增加它们对poly [I:C]的敏感性。干扰素α作为致敏剂效果较差。当巨噬细胞在抗小鼠干扰素α/β抗血清存在的情况下暴露于poly [I:C]时,B因子、C3和β-葡萄糖醛酸酶合成的变化会受到部分抑制。总体而言,这些数据表明,首先,将小鼠骨髓来源的巨噬细胞暴露于poly [I:C]会差异性地调节B因子、C3和β-葡萄糖醛酸酶基因产物的表达。其次,干扰素α和干扰素β使巨噬细胞致敏,以增加巨噬细胞对poly [I:C]的敏感性。第三,在没有外源性干扰素的情况下,巨噬细胞衍生的干扰素似乎以自分泌或旁分泌方式参与细胞的致敏过程。

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