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电离辐射可增加内皮细胞中血管性血友病因子基因的转录。

Ionizing irradiation increases transcription of the von Willebrand factor gene in endothelial cells.

作者信息

Jahroudi N, Ardekani A M, Greenberger J S

机构信息

Department of Radiation Oncology, University of Pittsburgh Medical Center, PA 15213, USA.

出版信息

Blood. 1996 Nov 15;88(10):3801-14.

PMID:8916944
Abstract

Ionizing irradiation damage to the vasculature results in an increase in procoagulant activity of endothelial cells, including elevated von Willebrand factor (vWf) secretion. We investigated the mechanism of irradiation induction of vWf release and demonstrated that vWf mRNA levels were increased when either human or bovine endothelial cells were exposed to 20 Gy irradiation. This response to irradiation was independent to de novo protein synthesis, but required new transcription. Nuclear run-on experiments indicated that increased vWf transcriptional activity was partly responsible for the higher levels of the mRNA accumulation. Transfection analyses with plasmids in which a human growth hormone structural gene was under the control of the endothelial-cell-specific vWf promoter demonstrated that irradiation increased promoter activity. Deletion analyses demonstrated that sequences necessary for irradiation induction of the promoter activity were located within the 112-bp sequences (-90 to +22) that constitute the non-endothelial-cell-specific core promoter region of the vWf gene. Results of gel mobility assays and deletion analyses demonstrated that a site in the vWf promoter other than the putative NF-kB binding site is involved in the mechanism of irradiation induction of the vWf.

摘要

电离辐射对脉管系统的损伤会导致内皮细胞促凝血活性增加,包括血管性血友病因子(vWf)分泌升高。我们研究了辐射诱导vWf释放的机制,并证明当人或牛内皮细胞暴露于20 Gy辐射时,vWf mRNA水平会升高。这种对辐射的反应不依赖于从头合成蛋白质,但需要新的转录。核转录实验表明,vWf转录活性增加是mRNA积累水平升高的部分原因。用人类生长激素结构基因受内皮细胞特异性vWf启动子控制的质粒进行转染分析表明,辐射增加了启动子活性。缺失分析表明,辐射诱导启动子活性所需的序列位于构成vWf基因非内皮细胞特异性核心启动子区域的112 bp序列(-90至+22)内。凝胶迁移分析和缺失分析结果表明,vWf启动子中除假定的NF-κB结合位点外的一个位点参与了辐射诱导vWf的机制。

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