病毒学报
病毒學報
병독학보
CHINESE JOURNAL OF VIROLOGY
2001年
1期
1-6
,共6页
任彩萍%蓝轲%冯湘玲%许亮国%何志巍%刘卫东%王慧%姚开泰
任綵萍%藍軻%馮湘玲%許亮國%何誌巍%劉衛東%王慧%姚開泰
임채평%람가%풍상령%허량국%하지외%류위동%왕혜%요개태
Epstein-Barr病毒%CR2基因%原位杂交%电镜观察
Epstein-Barr病毒%CR2基因%原位雜交%電鏡觀察
Epstein-Barr병독%CR2기인%원위잡교%전경관찰
EB病毒不能感染小鼠是因为小鼠CR2受体构像与人的不同。通过对小鼠CR2受体进行定点突变,然后将野生型和突变型小鼠CR2/1(MCR2/1)及人CR2(hCR2)用基因转移技术导入小鼠鼻咽上皮细胞系(TMNE)进行表达,观察转染阳性细胞是否具有结合EB病毒的能力。EBER-1杂交结果显示,只有转染hCR2和突变型MCR2(mtMCR2)的TMNE细胞可以感染EB病毒,但是前者感染EB病毒的阳性率比后者的高得多。电镜结果也进一步证实EB病毒可以感染这两种细胞。这为进一步研究EB病毒进入细胞的机制及建立EB病毒相关的鼻咽癌动物模型奠定了良好的基础。
EB病毒不能感染小鼠是因為小鼠CR2受體構像與人的不同。通過對小鼠CR2受體進行定點突變,然後將野生型和突變型小鼠CR2/1(MCR2/1)及人CR2(hCR2)用基因轉移技術導入小鼠鼻嚥上皮細胞繫(TMNE)進行錶達,觀察轉染暘性細胞是否具有結閤EB病毒的能力。EBER-1雜交結果顯示,隻有轉染hCR2和突變型MCR2(mtMCR2)的TMNE細胞可以感染EB病毒,但是前者感染EB病毒的暘性率比後者的高得多。電鏡結果也進一步證實EB病毒可以感染這兩種細胞。這為進一步研究EB病毒進入細胞的機製及建立EB病毒相關的鼻嚥癌動物模型奠定瞭良好的基礎。
EB병독불능감염소서시인위소서CR2수체구상여인적불동。통과대소서CR2수체진행정점돌변,연후장야생형화돌변형소서CR2/1(MCR2/1)급인CR2(hCR2)용기인전이기술도입소서비인상피세포계(TMNE)진행표체,관찰전염양성세포시부구유결합EB병독적능력。EBER-1잡교결과현시,지유전염hCR2화돌변형MCR2(mtMCR2)적TMNE세포가이감염EB병독,단시전자감염EB병독적양성솔비후자적고득다。전경결과야진일보증실EB병독가이감염저량충세포。저위진일보연구EB병독진입세포적궤제급건립EB병독상관적비인암동물모형전정료량호적기출。
Epstein-Barr virus(EBV) can not infect mouse naturally becausemouse CR2 receptor's conformation is different from human CR2 receptor. Method for site-directed mutagenesis was used to introduce two desired mutations into mouse complement receptor type Ⅱ gene(MCR2), which were confirmed by DNA sequencing. Then the constructed eukaryotic expression vectors containing wild type mouse CR2/1(wtMCR2/1) and mutant type mouse CR2/1 (mtMCR2/1) were transferred separately into mouse TMNE cells by LipofectAMINE as well as expression vector inserted with human CR2 (hCR2) cDNA. After long-term screening by G418, the stably transfected clones were obtained. Several ways including PCR, RT-PCR and immunohistochemistry were utilized to screen those clones with interested genes integrated and expressed. To explore whether these transfected cells could be infected by EBV, in situ hybridization method was utilized to detect the expression of EBV encoded RNAs (EBER-1) in the transfected mouse TMNE cells. The results showed that only hCR2 and mtMCR2 transfected TMNE cells could be infected by EBV, but the positive rate of EBER-1 in hCR2-expressed TMNE cells was much higher than that in mtMCR2-expressed TMNE cells. The observation results of electron microscope also showed that EBV could infect hCR2 and mtMCR2 transfected TMNE cells. This study sets groundwork for elucidating the mechanism by which EBV enters the cells and also provides possibility to establish EBV-related NPC animal model.