Mikovits J, Ruscetti F, Zhu W, Bagni R, Dorjsuren D, Shoemaker R
Laboratory of Antiviral Drug Mechanisms, SAIC Frederick, NCI-FCRDC, PO Box B, Bldg. 439, Frederick, MD 21702-1201, USA.
Dis Markers. 2001;17(3):173-8. doi: 10.1155/2001/896953.
Expression profiling of cellular genes was performed using a 10,000 cDNA human gene array in order to identify expression changes following chronic infection of human hematopoietic cells with Kaposi's Sarcoma-associated Virus (KSHV) also known as Human Herpesvirus 8 (HHV8) and Human T cell leukemia virus-1 (HTLV-1). We performed cell-free in vitro infection of primary bone marrow derived CD34+ cells using semi-purified HHV8 and a mature IL-2 dependent T cell line, KIT 225, using highly concentrated viral stocks prepared from an infectious molecular clone of HTLV-1. Thirty days post infection, mRNA was isolated from infected cultures and uninfected controls and submitted for microarray analysis. More than 400 genes were differentially expressed more than two-fold following HHV8 infection of primary bone marrow derived CD34+ cells. Of these 400, interferon regulatory factor 4 (IRF4), cyclin B2, TBP-associated factor, eukaryotic elongation factor and pim 2 were up-regulated more than 3.5 fold. In contrast, less than 100 genes were differentially expressed more than two-fold following chronic infection of a mature T cell line with HTLV-1. Of these, only cdc7 was up-regulated more than 3.5 fold. These data may provide insight into cellular signatures of infection useful for diagnosis of infection as well as potential targets for therapeutic intervention.
为了确定人类造血细胞被卡波西肉瘤相关病毒(KSHV,也称为人类疱疹病毒8型[HHV8])和人类T细胞白血病病毒1型(HTLV-1)慢性感染后的表达变化,我们使用10000个cDNA的人类基因芯片进行了细胞基因表达谱分析。我们使用半纯化的HHV8对原代骨髓来源的CD34+细胞进行无细胞体外感染,并使用从HTLV-1感染性分子克隆制备的高浓度病毒储备液对成熟的IL-2依赖T细胞系KIT 225进行感染。感染后30天,从感染培养物和未感染对照中分离mRNA并提交进行微阵列分析。原代骨髓来源的CD34+细胞被HHV8感染后,超过400个基因的表达差异超过两倍。在这400个基因中,干扰素调节因子4(IRF4)、细胞周期蛋白B2、TBP相关因子、真核延伸因子和pim 2的上调超过3.5倍。相比之下,成熟T细胞系被HTLV-1慢性感染后,差异表达超过两倍的基因不到100个。其中,只有细胞分裂周期蛋白7(cdc7)的上调超过3.5倍。这些数据可能有助于深入了解感染的细胞特征,从而有助于感染的诊断以及治疗干预的潜在靶点。