中国病毒学
中國病毒學
중국병독학
VIROLOGICA SINICA
2001年
2期
175-178
,共4页
吴海祥%郑从义%屈三甫%郭荆哲%王燕丽
吳海祥%鄭從義%屈三甫%郭荊哲%王燕麗
오해상%정종의%굴삼보%곽형철%왕연려
细胞凋亡%口蹄疫病毒%宿主细胞%致细胞病变效应
細胞凋亡%口蹄疫病毒%宿主細胞%緻細胞病變效應
세포조망%구제역병독%숙주세포%치세포병변효응
本文报道了口蹄疫病毒(Foot-and-Mouth Disease Virus, FMDV)在体外诱导PK-15细胞凋亡的研究结果。采用Hoechst33258荧光探针、DNA凝胶电泳、脱氧核糖核酸转移酶介导的缺口末端标记(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4.8 lgTCID50/mL的口蹄疫病毒感染PK-15细胞,在培养32?h 后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凝胶电泳显示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凋亡,细胞凋亡是其致细胞病变死亡的重要途径之一。
本文報道瞭口蹄疫病毒(Foot-and-Mouth Disease Virus, FMDV)在體外誘導PK-15細胞凋亡的研究結果。採用Hoechst33258熒光探針、DNA凝膠電泳、脫氧覈糖覈痠轉移酶介導的缺口末耑標記(TUNEL)技術均檢測到瞭典型的細胞凋亡。結果顯示:使用感染性滴度為4.8 lgTCID50/mL的口蹄疫病毒感染PK-15細胞,在培養32?h 後熒光探針檢測呈現典型的凋亡細胞覈固縮和梅花狀碎裂覈,併伴隨有凋亡小體齣現,凋亡率約為20%;DNA凝膠電泳顯示ladder梯帶;末耑標記檢測到彊綠色熒光標記物結閤于凋亡細胞覈上。研究結果提示:口蹄疫病毒可以在體外誘導宿主細胞凋亡,細胞凋亡是其緻細胞病變死亡的重要途徑之一。
본문보도료구제역병독(Foot-and-Mouth Disease Virus, FMDV)재체외유도PK-15세포조망적연구결과。채용Hoechst33258형광탐침、DNA응효전영、탈양핵당핵산전이매개도적결구말단표기(TUNEL)기술균검측도료전형적세포조망。결과현시:사용감염성적도위4.8 lgTCID50/mL적구제역병독감염PK-15세포,재배양32?h 후형광탐침검측정현전형적조망세포핵고축화매화상쇄렬핵,병반수유조망소체출현,조망솔약위20%;DNA응효전영현시ladder제대;말단표기검측도강록색형광표기물결합우조망세포핵상。연구결과제시:구제역병독가이재체외유도숙주세포조망,세포조망시기치세포병변사망적중요도경지일。
Apoptosis of PK-15 cells induced by Foot-and-Mouth Disease Virus (FMDV) in vitro was reported in this paper. Typical cell apoptosis was detected by use of Hoechst 33258 fluorescence probe, agarose gel electrophoresis and in situ end-labeling (TUNEL). After PK-15 cells were infected by titration of 4.8 lg TCID50/mL FMDV for 32 h, apoptosis characteristics of nuclear condensation, fragmentation, accompanied by apoptotic bodies formation (Hoechst 33258 staining), 180-200 integer-fold sized pieces DNA Ladders (agarose gel electrophoresis) and strong green fluorescence dots (TUNEL) were all exhibited, and cell apoptosis was approximately 20%. In addition, the quantitative analysis of apoptosis in PK-15 cells induced by FMDV showed that apoptosis was correlated with infection of virus, and it was also time-dependent. Results indicate that FMDV can induce apoptosis of host cells and apoptosis plays an important role in the cytopathogencity effect of FMDV.