C/T conversion alters interleukin-1A promoter function in a human astrocyte cell line

被引:13
作者
Wei, Xing
Chen, Xianming
Fontanilla, Christine
Zhao, Liming
Liang, Zhong
Dodel, Richard
Hampel, Hampel
Farlow, Martin
Du, Yansheng
机构
[1] Indiana Univ, Sch Med, Dept Neurol, Indianapolis, IN 46202 USA
[2] Univ Marburg, Dept Neurol, Marburg, Germany
[3] Univ Munich, Dept Psychiat, D-8000 Munich, Germany
关键词
Alzheimer's disease; interleukin-1; alpha; neuroinflammation; neurodegeneration; promoter polymorphism; A-beta; LPS;
D O I
10.1016/j.lfs.2006.12.011
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recently, association of an interleukin-1A promoter polymorphism (-889, thymine/thymine (T/T)) with Alzheimer's disease was reported, suggesting that this cytokine may play an important role in disease development. To understand the mechanism underlying the interleukin-1A promoter's role in Alzheimer's disease, a study comparing promoter function of an interleukin-1A polymorphism was performed in the SVG astroglia cell line. The effects of thymine and cytosine on transcriptional activity of the interleukin-1A promoter were analyzed by testing luciferase-reporter activity in transfected SVG cells. Our results demonstrate that cytosine/thymine conversion increases activity of the interleukin-1A promoter in SVG cells. Both sodium salicylate and lovastatin are able to block induced promoter activities in astroglial cells. Induced promoter activity by the polymorphism (T/T) may result in the upregulation of interleukin-1 alpha protein and "cytokine cycle" amplification, which may promote disease development. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1152 / 1156
页数:5
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