Early apoptosis-related changes triggered by HSV-1 in individual neuronlike cells

被引:23
作者
Gautier, I
Coppey, J
Durieux, C
机构
[1] Univ Paris 06, UMR 7592, Inst Jacques Monod, F-75251 Paris 05, France
[2] Univ Paris 07, UMR 7592, Inst Jacques Monod, F-75251 Paris, France
关键词
HSV-1; apoptosis; mitochondrial membrane potential; phosphatidyl serine; caspase; neuronal cell ND7; fluorescence microscopy;
D O I
10.1016/S0014-4827(03)00258-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Early events of apoptosis following HSV-1 infection were investigated at the single-cell level using intensified fluorescence digital-imaging microscopy. The results provide evidence that infection of differentiated ND7 neuronlike cells by HSV-1 triggers detectable alterations indicative of physiological changes associated with the early stages of apoptosis. Less than 1 h after infection with HSV-1 (KOS strain) or K26GFP (GFP being fused to HSV-1 capsid protein VP26) we observed (i) moderate decrease in mitochondrial membrane potential (about 20%), (ii) exposure of phosphatidyl serine, (iii) morphological change in the mitochondria that became spherical instead of filamentous, and (iv) activation of caspase-8. Within 3 h changes reverted to normal, which indicated that apoptosis was counteracted very early following HSV-1 infection. Similar results were obtained with KOS-TK(27)GFP, lacking TK and UL24 proteins, suggesting that TK and UL24 play no role in apoptosis. In Vero cells mitochondrial changes characteristic of the apoptotic process were not observed following HSV-1 infection. The UV-inactivated K26GFP had the capacity to induce apoptosis in neuronlike cells. This real-time multiparametric analysis, in combination with relevant viral mutants, could be a useful approach for dissecting the roles of various viral genes in modulating apoptotic pathways during infection. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:174 / 183
页数:10
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