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纳米粒子介导Egr-1DNA酶转染抑制移植静脉内膜增生

刘程伟 张雪松 王石 王树卿 田浩 程明勋 胡新华 辛世杰 段志泉

中国组织工程研究2012,Vol.16Issue(8):1354-1358,5.
中国组织工程研究2012,Vol.16Issue(8):1354-1358,5.DOI:10.3969/j.issn.1673-8225.2012.08.006

纳米粒子介导Egr-1DNA酶转染抑制移植静脉内膜增生

Transfection of early growth response gene-1 DNA enzyme mediated by nanoparticles inhibits vein graft intimal hyperplasia

刘程伟 1张雪松 1王石 1王树卿 1田浩 1程明勋 1胡新华 2辛世杰 2段志泉2

作者信息

  • 1. 佳木斯大学附属第一医院普外一科,黑龙江省佳木斯市,154003
  • 2. 中国医科大学附属第一医院血管外科,辽宁省沈阳市,110001
  • 折叠

摘要

Abstract

BACKGROUND: The method of gene has been admitted to prevent stenosis and occlusion of grafted vascular. But it is a hot spotof how to increase gene transfection efficiency.OBJECTIVE: To study the effect of partial transfection of exogenous early growth response gene-1 DNA enzyme (Egr-1 DNAenzyme, EDRz) mediated by nanoparticles (NP) on the intimal hyperplasia (IH) in grafted vein.METHODS: The EDRz was constructed. Nanoparticle EDRz complex was prepared with polylactic/poly glycolic acid (PLGA) andpolyvinyl alcohol (PVA). Autogenously vein graft model was established, and the 210 rats were divided into three groups randomly:(1) EDRz group, EDRz mediated by NP was transfected into the veins before anastomosis. (2) Empty vector group, the vein wastransfected by empty vector mediated by NP. (3) Control group, no transfection.RESULTS AND CONCLUSION: In EDRz group, the expression of mRNA and protein of Egr-1 gene in intimal was significantdecreased than that in other two groups (P < 0.05) and at the 7th, 14th and 28th days, the thickness of intimal hyperplasia wasdecreased than that in other two groups (P < 0.01), the apoptotic percentage of vascular smooth muscle cells in EDRz group wassignificant increased than that in other two groups (P < 0.05). EDRz expression can prevent intimal hyperplasia and promoteapoptosis of vascular smooth muscle cells after autogenous vein grafting.

关键词

纳米粒子/DNA 酶/移植静脉/转染/血管平滑肌细胞

分类

医药卫生

引用本文复制引用

刘程伟,张雪松,王石,王树卿,田浩,程明勋,胡新华,辛世杰,段志泉..纳米粒子介导Egr-1DNA酶转染抑制移植静脉内膜增生[J].中国组织工程研究,2012,16(8):1354-1358,5.

基金项目

国家自然科学基金资助项目(30801123,30872527). (30801123,30872527)

中国组织工程研究

OACSCDCSTPCD

2095-4344

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