›› 1995, Vol. 15 ›› Issue (4): 193-197.

• 论文 •    下一篇

重组真核表达载体介导的mUK基因转移及其在小鼠体内的表达

  

  1. 1.上海医科大学中山医院,上海市心血管病研究所;2.上海医科大学基础医学院
  • 收稿日期:1995-06-16 出版日期:1995-01-25 发布日期:2013-03-19
  • 基金资助:

    上海医科大学基因治疗基金

In Vivo Gene Transfer and Expression in Mice with Eukaryotic Expression Vector Containing Human mUK cDNA

  1. 1.Zhong Shan Hospital, Shanghai Medical University Shanghai Institute of Cardiovascular Diseases,Shanghai 200032;2.Laboratory of Molecular Genetics, Shanghai Medical University
  • Received:1995-06-16 Online:1995-01-25 Published:2013-03-19

摘要: 为研究以基因转移技术治疗血栓性疾病的可能性,将30只普通级雄性昆明小鼠随机均分为6组,第1~4组腹腔注射含人小分子量尿激酶(mUK)基因的重组质粒pcDNA3mUK,剂量分别为20、40、60和80ug/只;第5、6组为对照,分别注射pcDNA3和转染液。血浆mUK活性用S239O发色底物分光光度法测定。注射后,对照组的血浆mUK活性无显著变化;第1~4组的mUK活性逐渐升高,第10天达高峰,峰值分别为1400±170、2200±220、3050±340和3350±260IU/L。后3组的mUK活性显著高于注射前(940±200IU/L,n=30),至注射后60d,仍显著高于注射前(P<0.05)。这表明裸露质粒腹腔内注射能升高小鼠血浆纤溶活性,可能为血栓性疾病的防治提供新途径。

关键词: 人小分子量尿激酶, 重组质粒, 基因转移, 血浆纤溶活性, 小鼠

Abstract: The possibility of treating thrombosis diseases by gene transfer was studied with eukaryotic expression vector containing human mUK cDNA. Thirty Kunming mice were divided into 6 groups. The doses (ip) of pcDNA 3 mUK in group 1—4 were 20, 40, 60, 80 pig/mouse respectively. The other 2 groups were injected intraperitoneally with pcDNA 3 and transfection solution respectively as controls. The plasma mUK activity was measured with synthetic—peptide substrate S 2390. They increased significantly (P<0.05) in group 2-4 from the 5th to the 60th day after the injection as compared with those before the injection (940±200 IU/L, n=30), and reached the peaks of 2200±220, 3050±340,3350±260 IU/L respectively 10 days after the injection. The result suggests that the method of injection with recombinant plasmid containing human mUK cDNA may be applied to the prevention and treatment of thrombosis diseases.

Key words: "Micro-urokinase, Recombinant plasmid, Gene transfer, Plasma fibrinolytic activity, Mouse "