Department of Biomedical Engineering, Duke University, Durham, North Carolina 27708, USA.
Am J Physiol Heart Circ Physiol. 2010 Sep;299(3):H837-46. doi: 10.1152/ajpheart.00002.2010. Epub 2010 Jun 11.
Atherosclerotic plaques tend to form in the major arteries at certain predictable locations. As these arteries vary in atherosusceptibility, interarterial differences in endothelial cell biology are of considerable interest. To explore the origin of differences observed between typical atheroprone and atheroresistant arteries, we used DNA microarrays to compare gene expression profiles of harvested porcine coronary (CECs) and iliac artery endothelial cells (IECs) grown in static culture out to passage 4. Fewer differences were observed between the transcriptional profiles of CECs and IECs in culture compared with in vivo, suggesting that most differences observed in vivo were due to distinct environmental cues in the two arteries. One-class significance of microarrays revealed that most in vivo interarterial differences disappeared in culture, as fold differences after passaging were not significant for 85% of genes identified as differentially expressed in vivo at 5% false discovery rate. However, the three homeobox genes, HOXA9, HOXA10, and HOXD3, remained underexpressed in coronary endothelium for all passages by at least nine-, eight-, and twofold, respectively. Continued differential expression, despite removal from the in vivo environment, suggests that primarily heritable or epigenetic mechanism(s) influences transcription of these three genes. Quantitative real-time polymerase chain reaction confirmed expression ratios for seven genes associated with atherogenesis and over- or underexpressed by threefold in CECs relative to IECs. The present study provides evidence that both local environment and vascular bed origin modulate gene expression in arterial endothelium. The transcriptional differences observed here may provide new insights into pathways responsible for coronary artery susceptibility.
动脉粥样硬化斑块往往在某些可预测的位置形成于大血管。由于这些动脉的动脉粥样易感性不同,动脉间内皮细胞生物学的差异具有相当大的意义。为了探索在典型的易患动脉和抗动脉粥样硬化动脉之间观察到的差异的起源,我们使用 DNA 微阵列比较了在静态培养中生长至第 4 代的收获的猪冠状动脉(CEC)和髂动脉内皮细胞(IEC)的基因表达谱。与体内相比,培养物中 CEC 和 IEC 的转录谱之间观察到的差异较小,这表明体内观察到的大多数差异是由于两条动脉中独特的环境线索所致。单类微阵列的显著性揭示了大多数体内动脉间差异在培养物中消失,因为在传代后,在 5%假发现率下,85%的基因的折叠差异不显著,这些基因在体内被鉴定为差异表达。然而,HOXA9、HOXA10 和 HOXD3 这三个同源盒基因在冠状动脉内皮中的表达仍然至少分别低至 9 倍、8 倍和 2 倍。尽管从体内环境中去除,但持续的差异表达表明,这些三个基因的转录主要受到遗传或表观遗传机制的影响。定量实时聚合酶链反应证实了与动脉粥样硬化形成相关的七个基因的表达比值,并且在 CEC 中相对于 IEC 过表达或低表达三倍。本研究提供了证据表明,局部环境和血管床起源均调节动脉内皮中的基因表达。这里观察到的转录差异可能为导致冠状动脉易感性的途径提供新的见解。