Nasirudeen A M A, Liu Ding Xiang
Institute of Molecular and Cell Biology, Proteos, Singapore, Singapore.
J Med Virol. 2009 Jun;81(6):1069-81. doi: 10.1002/jmv.21486.
Recently, a dengue virus-induced apoptosis p53- and mitochondria-mediated were reported in human and animal cells. To understand further the underlying mechanisms, a p53-deficient cell line, H1299, and a p53-knockin cell line, H273, were infected with dengue type 1 virus and the cellular gene expression profiles at the mRNA level were analyzed by affymetrix array analysis. The results showed 183 genes with at least twofold increase at mRNA expression level in dengue virus-infected cells. Among the 183 genes, 68 genes were up-regulated in both H1299 and H273 cells and 78 genes were found to be up-regulated in only H273 cells. Eleven selected genes, mainly involved in IFN-pathway, cell cycle, signal transduction, and ubiquitin-proteasome pathways were confirmed using qualitative and quantitative PCR. Interestingly, an approximately 32-fold increase in caspase-1 expression was observed in the p53-knockin cell line, H273. Gene silencing of caspase-1 or inhibition of caspase-1 activity led to reduction in dengue virus-induced apoptosis with minimal effect on virus replication.
最近,有报道称登革病毒可在人和动物细胞中诱导p53和线粒体介导的凋亡。为了进一步了解其潜在机制,用1型登革病毒感染了p53缺陷细胞系H1299和p53敲入细胞系H273,并通过Affymetrix芯片分析在mRNA水平分析细胞基因表达谱。结果显示,登革病毒感染细胞中183个基因的mRNA表达水平至少增加了两倍。在这183个基因中,68个基因在H1299和H273细胞中均上调,78个基因仅在H273细胞中上调。使用定性和定量PCR确认了11个主要参与IFN通路、细胞周期、信号转导和泛素-蛋白酶体通路的选定基因。有趣的是,在p53敲入细胞系H273中观察到caspase-1表达增加了约32倍。caspase-1基因沉默或caspase-1活性抑制导致登革病毒诱导的凋亡减少,而对病毒复制的影响最小。