Dabek Józefa, Owczarek Aleksander, Gasior Zbigniew, Ulczok Rafal, Skowerski Mariusz, Kułach Andrzej, Mazurek Urszula, Bochenek Andrzej
Department of Cardiology, Medical University of Silesia, Ziołowa 47, Katowice, Poland.
Biochem Genet. 2008 Jun;46(5-6):241-7. doi: 10.1007/s10528-007-9137-3.
The pathology of cardiomyocyte death during and after myocardial infarction involves both necrosis and apoptosis. Although both mechanisms lead to cell death, participation of apoptosis in this process carries the potential of developing therapies influencing at least part of the population of dying cells. Therefore the aim of this study was to determine (using oligonucleotide microarrays) expression profiles of apoptosis-regulating genes in postinfarction myocardium, comparing chronically ischemic and healthy heart muscle. Tissue samples were obtained during elective surgery from the right cardiac auricles of three patients. The expression of 141 genes involved in fibrosis was assessed using the Affymetrix HG_U133A microarray. The patients' transcriptomes were compared using hierarchical clusterization. Differentiating genes were determined using regression analysis and Bland-Altman graph analysis. Hierarchical clusterization demonstrated that the profile of gene expression in postinfarction myocardium was different from that in the remaining specimens. Further statistical analysis showed two important differentiating genes: FOXO3A (underexpressed in post-MI sample) and CFLAR (overexpressed in post-MI sample). The expression of apoptosis-regulating genes is significantly different in post-MI myocardium from chronically ischemic and a nonischemic myocardium. Our results suggest that CFLAR is important in the induction of apoptosis in postinfarction cardiac tissue.
心肌梗死期间及之后心肌细胞死亡的病理过程涉及坏死和凋亡。尽管这两种机制都会导致细胞死亡,但凋亡在这一过程中的参与为开发至少能影响部分死亡细胞群体的治疗方法提供了可能性。因此,本研究的目的是(使用寡核苷酸微阵列)确定梗死心肌中凋亡调节基因的表达谱,并与慢性缺血心肌和健康心肌进行比较。组织样本取自三名患者择期手术期间的右心耳。使用Affymetrix HG_U133A微阵列评估141个参与纤维化的基因的表达。使用层次聚类法比较患者的转录组。使用回归分析和布兰德-奥特曼图分析确定差异基因。层次聚类表明梗死心肌中的基因表达谱与其余样本不同。进一步的统计分析显示了两个重要的差异基因:FOXO3A(在心肌梗死后样本中表达不足)和CFLAR(在心肌梗死后样本中表达过度)。梗死心肌中凋亡调节基因表达与慢性缺血心肌和非缺血心肌相比有显著差异。我们的结果表明,CFLAR在梗死心肌组织凋亡诱导中起重要作用。