Hussein Shaimaa, Michael Paul, Brabant Danielle, Omri Abdelwahab, Narain Ravin, Passi Kalpdrum, Ramana Chilakamarti V, Parrillo Joseph E, Kumar Anand, Parissenti Amadeo, Kumar Aseem
Int J Clin Exp Med. 2009 Jun 5;2(2):131-48.
To gain a better understanding of the gene expression changes that occurs during sepsis, we have performed a cDNA microarray study utilizing a tissue culture model that mimics human sepsis. This study utilized an in vitro model of cultured human fetal cardiac myocytes treated with 10% sera from septic patients or 10% sera from healthy volunteers. A 1700 cDNA expression microarray was used to compare the transcription profile from human cardiac myocytes treated with septic sera vs normal sera. Septic sera treatment of myocytes resulted in the down-regulation of 178 genes and the up-regulation of 4 genes. Our data indicate that septic sera induced cell cycle, metabolic, transcription factor and apoptotic gene expression changes in human myocytes. Identification and characterization of gene expression changes that occur during sepsis may lead to the development of novel therapeutics and diagnostics.
为了更好地理解脓毒症期间发生的基因表达变化,我们利用一种模拟人类脓毒症的组织培养模型进行了一项cDNA微阵列研究。本研究使用了体外培养的人胎儿心肌细胞模型,用脓毒症患者的10%血清或健康志愿者的10%血清进行处理。使用1700个cDNA表达微阵列比较用脓毒症血清处理的人心肌细胞与正常血清处理的人心肌细胞的转录谱。用脓毒症血清处理心肌细胞导致178个基因下调和4个基因上调。我们的数据表明,脓毒症血清诱导人心肌细胞的细胞周期、代谢、转录因子和凋亡基因表达发生变化。鉴定和表征脓毒症期间发生的基因表达变化可能会导致新型治疗方法和诊断方法的开发。