Hong J R, Lin T L, Yang J Y, Hsu Y L, Wu J L
Laboratory of Marine Molecular Biology and Biotechnology, Institute of Zoology, Academia Sinica, Nankang, Taipei 115, Taiwan, Republic of China.
J Virol. 1999 Jun;73(6):5056-63. doi: 10.1128/JVI.73.6.5056-5063.1999.
Morphologically, apoptotic cells are characterized by highly condensed membrane blebbing and formation of apoptotic bodies. Recently, we reported that apoptosis precedes necrosis in a fish cell line infected with infectious pancreatic necrosis virus (IPNV). In the present study, we tested the possibility that nontypical apoptosis is a component of IPNV-induced fish cell death. A variant type of green fluorescent protein (EGFP) was expressed in a fish cell line such that EGFP served as a protein marker for visualizing dynamic apoptotic cell morphological changes and for tracing membrane integrity changes during IPNV infection. Direct morphological changes were visualized by fluorescence microscopy by EGFP in living cells infected with IPNV. The nontypical apoptotic morphological change stage occurred during the pre-late stage (6 to 7 h postinfection). Nontypical apoptotic features, including highly condensed membrane blebbing, occurred during the middle apoptotic stage. At the pre-late apoptotic stage, membrane vesicles quickly formed, blebbed, and were finally pinched off from the cell membrane. At the same time, at this pre-late apoptotic stage, apoptotic cells formed unique small holes in their membranes that ranged from 0.39 to 0.78 micrometer according to examination by scanning electron microscopy and immunoelectron microscopy. Quantitation of the intra- and extracellular release of EGFP by CHSE-214-EGFP cells after IPNV infection was done by Western blotting and fluorometry. Membrane integrity was quickly lost during the late apoptotic stage (after 8 h postinfection), and morphological change and membrane integrity loss could be prevented and blocked by treatment with apoptosis inhibitors such as cycloheximide, genistein, and EDTA before IPNV infection. Together, these findings show the apoptotic features at the onset of pathology in host cells (early and middle apoptotic stages), followed secondarily by nontypical apoptosis (pre-late apoptotic stage) and then by postapoptotic necrosis (late apoptotic stage), of a fish cell line. Our results demonstrate that nontypical apoptosis is a component of IPNV-induced fish cell death.
从形态学上看,凋亡细胞的特征是高度浓缩的膜泡化和凋亡小体的形成。最近,我们报道了在感染传染性胰腺坏死病毒(IPNV)的鱼类细胞系中,凋亡先于坏死发生。在本研究中,我们测试了非典型凋亡是否是IPNV诱导的鱼类细胞死亡的一个组成部分。一种变异型绿色荧光蛋白(EGFP)在鱼类细胞系中表达,使得EGFP作为一种蛋白质标记物,用于观察IPNV感染期间动态的凋亡细胞形态变化以及追踪膜完整性变化。通过荧光显微镜观察感染IPNV的活细胞中EGFP,直接观察到形态学变化。非典型凋亡形态变化阶段发生在感染后期之前(感染后6至7小时)。包括高度浓缩的膜泡化在内的非典型凋亡特征出现在凋亡中期。在凋亡后期之前的阶段,膜泡迅速形成、泡化,最终从细胞膜上脱离。与此同时,在这个凋亡后期之前的阶段,凋亡细胞在其膜上形成独特的小孔,根据扫描电子显微镜和免疫电子显微镜检查,这些小孔的大小在0.39至0.78微米之间。通过蛋白质印迹法和荧光测定法对IPNV感染后CHSE - 214 - EGFP细胞中EGFP的细胞内和细胞外释放进行定量分析。在凋亡后期(感染后8小时后)膜完整性迅速丧失,在用环己酰亚胺、染料木黄酮和乙二胺四乙酸等凋亡抑制剂在IPNV感染前进行处理,可以预防和阻断形态学变化和膜完整性丧失。总之,这些发现显示了鱼类细胞系中宿主细胞病理发生初期(凋亡早期和中期)的凋亡特征,其次是非典型凋亡(凋亡后期之前的阶段),然后是凋亡后坏死(凋亡后期)。我们的结果表明,非典型凋亡是IPNV诱导的鱼类细胞死亡的一个组成部分。