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肿瘤坏死因子可增强内皮细胞中组织因子信使核糖核酸的表达。

Tumor necrosis factor enhances expression of tissue factor mRNA in endothelial cells.

作者信息

Conway E M, Bach R, Rosenberg R D, Konigsberg W H

机构信息

Department of Biology, Massachusetts Institute of Technology, Charles A. Dana Research Institute, Harvard-Thorndike Laboratory, Cambridge.

出版信息

Thromb Res. 1989 Feb 1;53(3):231-41. doi: 10.1016/0049-3848(89)90098-4.

Abstract

We have examined the effect of recombinant tumor necrosis factor on the expression of tissue factor activity and tissue factor mRNA levels in vascular endothelial cells. Following exposure of human umbilical vein endothelial cells to this cytokine, the appearance of tissue factor procoagulant activity was detected following cell disruption, and was maximal at 6 hours. Northern blot analysis of cytokine-treated cells demonstrated a similar increase in the synthesis of tissue factor mRNA, followed by a gradual decline to the basal level by 18 hours. Cycloheximide by itself induced the accumulation of high levels of tissue factor mRNA in these cells. This result suggests that the proteins necessary for transcription of the tissue factor gene are present in the endothelial cell prior to cytokine stimulation, and synthesis of the tissue factor mRNA may be controlled, in part, by a labile repressor protein.

摘要

我们研究了重组肿瘤坏死因子对血管内皮细胞中组织因子活性表达及组织因子mRNA水平的影响。将人脐静脉内皮细胞暴露于这种细胞因子后,细胞破碎后检测到组织因子促凝活性的出现,且在6小时时达到最大值。对经细胞因子处理的细胞进行Northern印迹分析表明,组织因子mRNA的合成有类似增加,随后到18小时逐渐降至基础水平。放线菌酮单独作用可诱导这些细胞中高水平组织因子mRNA的积累。这一结果表明,组织因子基因转录所需的蛋白质在细胞因子刺激之前就存在于内皮细胞中,组织因子mRNA的合成可能部分受不稳定的阻遏蛋白控制。

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