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程新刘宝玲王海滨金壮张杰林CrumpackerClyde人刘宝玲王海滨金壮张杰林CrumpackerClyde巨细胞病毒临床分离株感染血管内皮细胞伴肾素基因表达
引用本文:程远,李多多,程计林,程新,刘宝玲,王海滨,金壮,张杰林,Crumpacker Clyde.程新刘宝玲王海滨金壮张杰林CrumpackerClyde人刘宝玲王海滨金壮张杰林CrumpackerClyde巨细胞病毒临床分离株感染血管内皮细胞伴肾素基因表达[J].中国分子心脏病学杂志,2009(4):193-198.
作者姓名:程远  李多多  程计林  程新  刘宝玲  王海滨  金壮  张杰林  Crumpacker Clyde
作者单位:[1]上海市复旦大学附属公共卫生临床中心,上海市201508 [2]河南省新乡医学院生理学与神经生物学教研室,新乡市453003 [3]河南省新乡医学院第一附属医院小儿内一科,卫辉市453100 [4]The Division of Infectious Disease, Beth Israel Deaconess Medical Center, Harvard Medical School, Harvard University , USA [5]Woreest Polytechnic Institute in USA , Beth Israel Deaconess Medical Center, Harvard Medical School, Harvard University , USA [6]Massachusetts General Hospital, Harvard Medical School, Harvard University, USA
基金项目:基金项目:上海复旦大学医学院基础-临床交叉研究基金(JC08-7)、上海市复旦大学生物医学研究院(IBS)2008年度开放课题基金(20088100)和上海市(复旦大学附属)公共卫生临床中心引进人才科研启动基金(RCJJ17)
摘    要:目的探讨巨细胞病毒(Cytomegalovirus,CMV)是否感染血管内皮细胞伴肾素表达。方法(1)用10^7pfu(空斑形成单位)/mlCMV临床分离株BI-5和实验室型CMVAD169分别与10^6腹主动脉内皮细胞和人脐静脉内皮细胞共同孵育,在23小时后、第3天、第7天、第10天和第14天分别收集培养上清200μl,第14天用PBS缓冲液洗细胞3次,收获细胞。每组实验均设培养液代替病毒液的无感染对照;(2)COBAS定量PCR检测培养上清中CMVDNA拷贝数;(3)PCR检测感染细胞中CMVpol基因;(4)RT—PCR、RealtimeRT—PCR和Westernblot检测肾素在感染细胞内的表达。结果(1)BI-5和AD169感染静脉和动脉细胞后,其形态学变化相似,无细胞裂解病理效应;(2)ADl69感染细胞不同时间培养上清中CMVDNA拷贝数无明显增加,BI-5呈增殖趋势;(3)BI-5感染动脉细胞CMVDNA拷贝数和肾素表达量均大于静脉细胞。结论临床分离株CMV以非裂解形式在血管内皮细胞持续存在并诱导肾素基因表达,血管内皮细胞分泌肾素可能是CMV感染引起心血管疾病的新机制。

关 键 词:巨细胞病毒  血管内皮细胞  肾素

Renin gene expression in the vascular endothelial cells infected by the dinical isolate of cytomegalovirus
Affiliation:CHENG Yuan , LI Duo-duo CHENG Ji-lin , CHENG Xin, LIU Bao-ling, WANG Hal-bin, JIN Zhnang, ZHANG Jie-lin, CRUMPACKER Clyde( 1 Shanghai Public Health Clinical Center affiliated to Fudan University, Shanghai , 201508, China; 2 Xinxiang Medical College in Henan Province, Xinxiang, 453003, China; 3 The First Hospital affiliated to Xinxiang Medical College in Henan Province, Weihui, 453100, China; 4The Division of lnfectious Disease, Beth Israel Deaconess Medical Center, Harvard Medical School, Harvard University, Boston, 02215, USA; 5 Worcest Polytechnic Institute in USA, Worcest , 01609, USA ; 6Massachusetts General Hospital, Harvard Medical School, Harvard University, Boston, 02114, USA.)
Abstract:Objective To explore whether or not cytomegalovirus (CMV) infected cardiovascular endothelial cells with renin gene expression. Methods ( 1 ) Umbilical vein cell line and abdominal aorta cell line were respectively infected with the clinical isolate of CMV BI-5 and the laboratory strain of CMV AD169 at multiplicities of infection (MOI) of 10 of each virus ( 107 pfu/ml CMV/106 ceils) and mock infected with medium alone. The supernatant of 200μl from each culture was collected at the 23rd hour, day 3, 7, 10, and 14 post-infection and replaced back with 200μl of fresh medium. At the 14th day of post-infection, the cells were rinsed with PBS three times and then harvested ; (2) CMV DNA copies in the supernatant from each cuhure were determined by COBAS PCR;(3) CMV DNA polymerase (pol) gene in the infected cells was tested by PCR; (4) The renin expression in the viral infected cells was measured with RT-PCR,real time quantity RT-PCT and western blot. Results ( 1 ) Lytic replication of CMV was not found in both venous and arterial cells infected till the 14th post-infective day; (2) The clinical isolates BI-5 persistently replicated in both venous and arterial endothelial cells and their supernatants but not the AD169, determined by viral pol gene copy number in both types of cells infected; (3) CMV DNA and renin expression in CMV infected arterial cells both were slronger than in venous cells. Conclusiou CMV was nonlytic and continuously released from the infected vascular cells for the life span of the culture, and induced renin expression in CMV-infected cells. The locat renin from CMV- infected cells possibly plays an important role in pathogenesis of atherosclerosis.
Keywords:Cytomegalovirus  vaseular endothelial Cells  Renin
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