首页 | 本学科首页   官方微博 | 高级检索  
     

人腺病毒3型感染对H9c2细胞microRNA表达谱的影响
引用本文:林乐勋,赵文然,佟雷,武帅钦,刘慧敏,刘惠彬,栾天,王博,马倩倩,钟照华. 人腺病毒3型感染对H9c2细胞microRNA表达谱的影响[J]. 国际免疫学杂志, 2009, 32(3): 173-175. DOI: 10.3760/cma.j.issn.1673-4394.2009.03.003
作者姓名:林乐勋  赵文然  佟雷  武帅钦  刘慧敏  刘惠彬  栾天  王博  马倩倩  钟照华
作者单位:哈尔滨医科大学微生物学教研室,150081;哈尔滨医科大学细胞生物学教研室
基金项目:中国博士后科学基金和黑龙江省博士后基金 
摘    要:目的研究腺病毒感染对大鼠心肌来源的H9c2细胞microRNA表达谱的影响。方法用人腺病毒3型(Ad3)攻击成层和未成层的H9c2细胞,6h后收获总RNA,基因芯片检测microRNA表达谱。结果比较未成层与成层的H9c2细胞microRNA的表达谱,H9c2细胞成层后有54种microRNA表达显著下调,7种microRNA表达显著上调。与未感染病毒的细胞比较,Ad3感染的未成层H9c2细胞有41种microRNA表达显著下调,12种microRNA表达显著上调。与未感染病毒的细胞比较,Ad3感染成层H9c2细胞后有8种microRNA的表达显著下调,62种microRNA的表达显著上调。结论细胞不同的生长状态及Ad3感染显著改变了H9c2细胞的microRNA表达谱。

关 键 词:人腺病毒  H9c2细胞  microRNA芯片  心肌炎

microRNA expression profile of H9c2 cells infected with human adenovirus type 3
Affiliation:LIN Le-xun. , ZHAO Wen-ran, TONG Lei, et al. (Department of Microbiology, Harbin Medical University, Harbin 150081, China)
Abstract:Objective To study the microRNA expression profile of rat myoeardium-derived H9c2 cells in-fected with human adenovirus type 3(Ad3).Methods Confluent and unconfluent H9c2 cells were attacked with Ad3.Six hour later total RNAs were harvested and microRNA expression profiling was analyzed by mi-cmRNA array.Results The expression of 54 microRNAs Was down-regulated and 7 micwRNAs Was up-reg-ulated in COnnuent H9c2 cells compared with that in unconiluent H9c2 cells.The expression of 41 miemR-NAs wag down-regulated and 12 Was up-regulated in unconfluent H9e2 cells infected with Ad3 compared with that in unconiluent H9c2 cells without Ad3 infection.There were 8 microRNAs down-regulated and 62 up-regulated in confluent H9c2 infected with Ad3 compared with that in comquent H9c2 ceils without Ad3 infec-tion.Condusion The microRNA expression profile,correlating with different cell growth states,was siguif-icanfly altered by human adenovirus infection.
Keywords:Human adenovirus  H9c2 cell  microRNA microarray  Myocarditis
本文献已被 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号