Graduate Institute and Department of Life Science, Tzu-Chi University, Hualien, Taiwan.
Arch Virol. 2011 Nov;156(11):1917-29. doi: 10.1007/s00705-011-1063-3. Epub 2011 Jul 22.
In this study, intracellular signaling in ARV S1133-mediated apoptosis was investigated. A microarray was used to examine the gene expression profiles of cells upon ARV S1133 infection and ARV-encoded pro-apoptotic protein σC overexpression. The analysis indicated that in the set of DNA-damage-responsive genes, DDIT-3 and GADD45α were both upregulated by viral infection and σC overexpression. Further investigation demonstrated that both treatments caused DNA breaks, which increased the expression and/or phosphorylation of DNA damage response proteins. ROS and lipid peroxidation levels were increased, and ARV S1133 and σC caused apoptosis mediated by DNA damage signaling. ROS scavenger NAC, caffeine and an ATM-specific inhibitor significantly reduced ARV S1133- and σC-induced DNA breaks, DDIT-3 and GADD45α expression, H2AX phosphorylation, and apoptosis. Overexpression of DDIT-3 and GADD45α enhanced the oxidative stress and apoptosis induced by ARV S1133 and σC. In conclusion, our results demonstrate the involvement of the DNA-damage-signaling pathway in ARV S1133- and σC-induced apoptosis.
在这项研究中,研究了 ARV S1133 介导的细胞凋亡中的细胞内信号转导。利用微阵列检测了 ARV S1133 感染和 ARV 编码的促凋亡蛋白 σC 过表达后细胞的基因表达谱。分析表明,在一组 DNA 损伤反应基因中,DDIT-3 和 GADD45α 均被病毒感染和 σC 过表达上调。进一步的研究表明,两种处理都导致了 DNA 断裂,从而增加了 DNA 损伤反应蛋白的表达和/或磷酸化。ROS 和脂质过氧化水平增加,ARV S1133 和 σC 通过 DNA 损伤信号诱导细胞凋亡。ROS 清除剂 NAC、咖啡因和 ATM 特异性抑制剂显著减少了 ARV S1133 和 σC 诱导的 DNA 断裂、DDIT-3 和 GADD45α 的表达、H2AX 磷酸化和细胞凋亡。DDIT-3 和 GADD45α 的过表达增强了 ARV S1133 和 σC 诱导的氧化应激和细胞凋亡。总之,我们的结果表明,DNA 损伤信号通路参与了 ARV S1133 和 σC 诱导的细胞凋亡。