期刊文献+

斑点叉尾呼肠孤病毒诱导斑点叉尾肾脏组织细胞凋亡的研究 被引量:1

Studies on the apoptosis of channel catfish(Ictalurus punetaus) kidney cells induced by channel catfish reovirus
在线阅读 下载PDF
导出
摘要 为研究斑点叉尾呼肠孤病毒(CCRV)诱导斑点叉尾肾脏细胞(CCK)发生凋亡的机理,以CCRV感染的CCK细胞为实验材料,采用Hoechst 33258染色、DNA片段化检测、TUNEL反应、亚G1期细胞检测以及线粒体膜电位变化检测等方法进行实验。感染试验结果显示,病毒感染斑点叉尾肾脏组织细胞后,细胞变圆、皱缩,随后细胞脱落,细胞单层呈网状,感染72h后出现典型细胞病变效应(CPE);病毒感染48 h后Hoechst 33258染色结果显示,细胞的染色质固缩、核边缘化或破裂,可观察到凋亡小体,细胞凋亡率随时间增加;DNA片段化检测结果显示,病毒感染细胞12 h后细胞基因组DNA出现片段化,随后逐渐增强,72 h达到最高;TUNEL反应结果表明,病毒感染细胞72 h后细胞基因组DNA断裂,有大量游离3'末端自由羟基(-OH)存在。亚G1期细胞检测结果显示,病毒感染48 h后,约53.44%细胞处于亚G1期;利用JC-1检测试剂盒检测病毒感染细胞的线粒体膜电位变化,病毒感染细胞24 h后线粒体膜通透性发生改变,膜电位变化显著。紫外线灭活与热灭活的斑点叉尾呼肠孤病毒不能诱导斑点叉尾肾脏细胞发生凋亡,表明细胞凋亡依赖于病毒复制。 Channel catfish reovirus(CCRV)is the pathogen of the hemorrhage of channel catfish(Ictalurus punctatus Rafinesque),which propagates in the kidney of channel catfish(CCK)cell line.In this study,the evaluation of whether the CCRV could induce the apoptosis of CCK cells was examined by Hoechst33258 staining,DNA fragmentation assay,TUNEL reaction,and flow cytometry analysis using JC-1,etc.The infection test indicated that CCRV caused typical cytopathic effect(CPE)in CCK cells.Chromatin condensation,nuclei marginalization and the apoptotic bodies were observed in Hoechst 33258 staining,and the apoptotic rate increased with the time going of CCRV infection.The DNA fragmentation assay demonstrated that fragmentation was first noted at 12 h post-infection and reached the peak at 72 h post-infection.In addition,genomic DNA was broken and lots of 3′-termianl free-hydroxyl group(-OH)were generated in infected CCK in TUNEL assay.The hypo-diploid fraction was shown in the sub-G1 cells analysis and the apoptotic rate was 53.44% at 48 h post-infection.Furthermore,the change of the mitochondrial membrane potential(MMP)was investigated by flow cytometric analysis with JC-1 fluorescent labeling and the result showed that the membrane permeability and MMP of CCK cells changed significantly at 24 h post-infection.These results demonstrated that CCRV induced apoptosis in CCK cells.Besides,CCRV-induced apoptosis did require the viral replication as the apoptosis was blocked in CCK cells by both heat-inactivated and UV-inactivated virus.
出处 《水产学报》 CAS CSCD 北大核心 2013年第1期117-124,共8页 Journal of Fisheries of China
基金 公益性行业(农业)科研专项(200803013)
关键词 斑点叉尾鮰 呼肠孤病毒 肾脏组织细胞系 细胞凋亡 Ictalurus punctatus reovirus kidney cell line apoptosis
  • 相关文献

参考文献24

  • 1梁智辉;朱慧芬;陈九武.流式细胞术基本原理与实用技术[M]武汉:华中科技大学出版社,20004-16.
  • 2王珊,周春喜,李宁,于力方,廖杰.检测早期细胞凋亡的流式细胞术[J].现代科学仪器,2003,20(3):48-50. 被引量:3
  • 3Pham P H,Lai Y S,Lee F F Y. Differential viral propagation and induction of apoptosis by grouper iridovirus(GIV) in cell lines from three nonhost species[J].Virus Research,2012,(01):16-25.
  • 4Huang Y H,Huang X H,Gui J F. Mitochondrion-mediated apoptosis induced by Rana grylio virus infection in fish cells[J].Apoptosis:An International Journal on Programmed Cell Death,2007,(09):1569-1577.
  • 5Chiu C L,Wu J L,Her G M. Aquatic birnavirus capsid protein,VP3,induces apoptosis via the Bad-mediated mitochondria pathway in fish and mouse cells[J].Apoptosis:An International Journal on Programmed Cell Death,2010,(06):653-668.
  • 6Hong J R,Huang L J,Wu J L. Aquatic birnavirus induces apoptosis through activated caspase-8 and-3 in a zebrafish cell line[J].Journal of Fish Diseases,2005,(03):133-140.doi:10.1111/j.1365-2761.2004.00604.x.
  • 7Hong J R,Gong H Y,Wu J L. IPNV VP5,a novel anti-apoptosis gene of the Bcl-2 family,regulates Mcl-1 and viral protein expression[J].Virology,2002,(02):217-229.doi:10.1006/viro.2001.1336.
  • 8Du C S,Zhang Q Y,Li CL. Induction of apoptosis in a carp leucocyte cell line infected with turbot(Scophthalmus maximus L.)rhabodovirus[J].Virus Research,2004,(02):119-126.doi:10.1016/j.virusres.2003.12.034.
  • 9DeWitte-Orr S J,Bols N C. Cytopathic effects of chum salmon reovirus to salmonid epithelial,fibroblast and macrophage cell lines[J].Virus Research,2007,(1-2):159-171.
  • 10屈三甫,张小榕,郑从义,胡国斌,艾桃山,丁桂珍,喻运珍,刘颖.鱼呼肠孤病毒诱导草鱼肾细胞凋亡[J].水生生物学报,2000,24(6):616-621. 被引量:7

二级参考文献126

共引文献151

同被引文献8

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部