Department of Cardiology, Medical University of Silesia, Katowice, Poland.
Inflammation. 2010 Dec;33(6):398-407. doi: 10.1007/s10753-010-9198-z.
Cardiovascular diseases, including acute coronary syndrome (ACS), are the leading cause of death among humans. Adhesion proteins, owing to their involvement in the initiation and progression of atherosclerotic lesions, contribute to the progression of coronary disease and ACS occurrence. Considering ambiguosity of results reported to date, we decided to conduct a preliminary investigation of adhesion protein gene expression in ACS patients as well as in healthy subjects by making use of oligonucleotide microarray technology. Analysis of eight microarrays revealed ten upregulated genes differentiating between the two groups: intercellular adhesion molecule-2, platelet/endothelial cell adhesion molecule-1, zyxin, integrin-linked kinase, calcium and integrin binding protein-1 (calmyrin), integrin beta 2, integrin beta 3 (ITGB3), integrin beta 7, integrin alpha 2b, and selectin P ligand. The expression of ITGB3 was found to have been downregulated.
心血管疾病,包括急性冠状动脉综合征(ACS),是人类死亡的主要原因。黏附蛋白因其参与动脉粥样硬化病变的发生和进展,促进了冠心病和 ACS 的发生。考虑到迄今为止报告的结果存在歧义,我们决定通过寡核苷酸微阵列技术初步研究 ACS 患者和健康受试者的黏附蛋白基因表达。对 8 个微阵列的分析显示,两组之间有 10 个上调基因:细胞间黏附分子-2、血小板/内皮细胞黏附分子-1、zyxin、整合素连接激酶、钙和整合素结合蛋白-1(钙调蛋白)、整合素β2、整合素β3(ITGB3)、整合素β7、整合素α2b 和选择素 P 配体。发现 ITGB3 的表达下调。