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山东大学学报(医学版)

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巨细胞病毒感染人脐静脉内皮细胞后RAGEmRNA的时序性表达及其意义

吴建敏,周亚滨,程轶?,李树英,唐伟,赵蔚明,贾继辉,栾怡,齐眉,王红,刘娟,于晗,于修平   

  1. 实验畸形学教育部重点实验室 山东大学医学院微生物学教研室, 山东 济南 250012
  • 收稿日期:2005-09-10 修回日期:1900-01-01 出版日期:2006-08-24 发布日期:2006-08-24
  • 通讯作者: 吴建敏

WU Jianmin, ZHOU Yabin, CHENG Yizhe, LI Shuying, TANG Wei, ZHAO Weiming, JIA JihuiLUAN Yi, QI Mei, WANG Hong, LIU Juan, YU Han, YU Xiuping   

  1. The Key Laboratory of Experimental Teratology, Ministy of Education, China; Department of Microbiology,School of Medicine, Shandong University, Jinan 250012, Shandong, China
  • Received:2005-09-10 Revised:1900-01-01 Online:2006-08-24 Published:2006-08-24

摘要: 目的:研究人巨细胞病毒(HCMV)感染对人脐静脉内皮细胞(HUVEC)糖基化终产物受体(RAGE)表达的影响,探讨HCMV感染致动脉粥样硬化的作用机制。方法:用HCMV感染HUVEC,采用RTPCR方法检测不同感染时段细胞RAGEmRNA的表达。结果:HCMV感染HUVEC后,0?h时RAGEmRNA有基础水平的表达,4?h开始升高,8?h时表达水平明显升高,随感染时间延长,表达量逐渐增高,感染24?h时达高峰,48?h开始回落,72?h表达量仍维持在较高的水平,显著高于0?h。各时段与0?h比较,均有统计学意义(P<0.01)。结论:HCMV感染人脐静脉内皮细胞后能够促进RAGE mRNA的表达,并且呈时间依赖性。HCMV有可能通过上调RAGE介导内皮细胞的炎症反应,促进动脉粥样硬化的发生、发展。

Abstract: To study the mechanims of cytomegalovirus infection by investigating the sequential changes of the receptor for advanced glycation end products in human umbilical vein endothelial cells with human cytomegalovirus infection. Methods: HUVEC was cultured and then infected by HCMV. Expression of RAGE mRNA was detected by reverse transcriptase polymerase chain reaction. Results: RAGE mRNA was expressed at a low level in control group, and began to increase 4 hours after HCMV infection, rose to a significant level at 12 hours, reached the peak at 24 hours. After 48 hours, it declined obviously and remained a relatively high level at 72 hours (P<0.01). Conclusions: HCMV infection can enhance the expression of RAGE mRNA in HUVEC in a timeeffect fashion, and may induce the inflammatory reaction by upregulating RAGE expression on endothelial cells, which facilitate the occurrence and development of atherosclerosis

Key words: Human cytomegalovirus, Infection, Receptor, the receptor for advanced glycation end products, Human umbilical vein endothelial cells

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