Universite Lyon1, INSERM, ERI22, EA 4173, Lyon, France.
J Biosci. 2013 Jun;38(2):311-5. doi: 10.1007/s12038-013-9310-2.
Classic characteristics are poor predictors of the risk of thromboembolism. Thus, better markers for the carotid atheroma plaque formation and symptom causing are needed. Our objective was to study by microarray analysis gene expression of genes involved in homeostasis of iron and heme in carotid atheroma plaque from the same patient. mRNA gene expression was measured by an Affymetrix GeneChip Human Gene 1.0 ST arrays (Affymetrix, Santa Clara, CA, USA) using RNA prepared from 68 specimens of endarteriectomy from 34 patients. Two genes involved in iron-heme homeostasis, CD163 and heme oxygenase (HO-1), were analysed in 34 plaques. CD163 (2.18, p01.45E-08) and HO-1 (fold-change 2.67, p02.07E-09) mRNAs were induced. We suggest that atheroma plaques show a more pronounced induction of CD163 and HO-1. Although further evidence is needed, our results support previous data. To our knowledge, this is the first report comparing gene expression between intact arterial tissue and carotid plaque using microarray analysis.
经典特征是血栓栓塞风险的不良预测因子。因此,需要更好的标志物来预测颈动脉粥样硬化斑块形成和导致症状的标志物。我们的目的是通过微阵列分析研究同一位患者颈动脉粥样硬化斑块中参与铁和血红素稳态的基因的基因表达。使用从 34 名患者的 68 份内膜切除术标本中制备的 RNA,通过 Affymetrix GeneChip Human Gene 1.0 ST 阵列(Affymetrix,Santa Clara,CA,USA)测量 mRNA 基因表达。在 34 个斑块中分析了两个参与铁血红素稳态的基因,CD163 和血红素加氧酶(HO-1)。CD163(2.18,p01.45E-08)和 HO-1(倍数变化 2.67,p02.07E-09)mRNA 被诱导。我们认为动脉粥样硬化斑块显示出更明显的 CD163 和 HO-1 诱导。尽管需要进一步的证据,但我们的结果支持先前的数据。据我们所知,这是首次使用微阵列分析比较完整动脉组织和颈动脉斑块之间基因表达的报告。