WU Hai, ZHENG Cong, QU San, WANG Yan and Studies on Apoptosis of Host Cells Induced by Foot-and-M outh Disease Virus[J]. Virologica Sinica, 2001, 16(2): 175-178.
Citation: WU Hai, ZHENG Cong, QU San, WANG Yan, . Studies on Apoptosis of Host Cells Induced by Foot-and-M outh Disease Virus .VIROLOGICA SINICA, 2001, 16(2) : 175-178.

口蹄疫病毒诱导宿主细胞凋亡的研究

  • 本文报道了口蹄疫病毒(F∞t—and-Mouth Disease Vh’us FMDV)在体外诱导PK.15细胞消亡的研究结果。采 用Hoechst33258荧光探针、DNA凝胶电泳、脱氧核搪核酸转移酶舟导的缺口末端标记(TUNEL)技术均检测到了 典型的细胞凋亡 结果显示:使用感染性滴度为4 8lgTCI /mL的口蹄疫病毒感染PK一15细胞,在培养32 h后r 荧光探针检测呈现典型的凋亡细胞核固缩和梅花状碎裂核,并伴随有凋亡小体出现,凋亡率约为20% ;DNA凝胶 电诛显示ladder梯带;末端标记检测到强绿色荧光标记物结合于凋亡细胞核上 研究结果提示:口蹄疫病毒可以 在体外诱导宿主细胞隅亡,细胞偶亡是其致细胞病交死亡的重要途径之一。

Studies on Apoptosis of Host Cells Induced by Foot-and-M outh Disease Virus

  • Apoptosis of PK—t5 ceils induced by Foot—and-Mouth Disease Virus(FMDV)in vitro was reported in this paper.Typical cell apoptosis was detected hy ti.se of Hoechst 33258 fluorescence probe. agarose gel electrophoresis and in situ end-labeling(TUNEL).After PK一15 cells were infected by titration of 4.8 lg TCIDsD/mL FMDV for 32 h,apoptosis characteristics of nuclear condensation, fragmentation,accompanied by apoptotic bodies formation(Hoeehst 33258 staining).180—200 inte— ger-fold sized pieces DNA Ladders(agarose gel e1.ectrophoresis)and strong green fluorescence clots (TUNEL)were alI exhibited,and cell apoptosis was approximately 20% In addition.the quantira— tire analysis of apoptosis in PK一15 ceils induced by FMDV showed that apoptosis was correlated with infection of virus.and it was also tim~dependent.Results indicare that FMDV can induce apoptosis of host ceils and apoptosis plays an important role in the cytopathogencity effect of FMDV

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    Studies on Apoptosis of Host Cells Induced by Foot-and-M outh Disease Virus

    • 1. College of Life Sciences,Wuhan University Wuhan 430072,China

    Abstract: Apoptosis of PK—t5 ceils induced by Foot—and-Mouth Disease Virus(FMDV)in vitro was reported in this paper.Typical cell apoptosis was detected hy ti.se of Hoechst 33258 fluorescence probe. agarose gel electrophoresis and in situ end-labeling(TUNEL).After PK一15 cells were infected by titration of 4.8 lg TCIDsD/mL FMDV for 32 h,apoptosis characteristics of nuclear condensation, fragmentation,accompanied by apoptotic bodies formation(Hoeehst 33258 staining).180—200 inte— ger-fold sized pieces DNA Ladders(agarose gel e1.ectrophoresis)and strong green fluorescence clots (TUNEL)were alI exhibited,and cell apoptosis was approximately 20% In addition.the quantira— tire analysis of apoptosis in PK一15 ceils induced by FMDV showed that apoptosis was correlated with infection of virus.and it was also tim~dependent.Results indicare that FMDV can induce apoptosis of host ceils and apoptosis plays an important role in the cytopathogencity effect of FMDV

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