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Construction and biological activities of human tPA eukaryotic expression plasmid

Construction and biological activities of human tPA eukaryotic expression plasmid

作     者:Zhong-Jun Wu Su-Fen Yang Shu-Sen Zheng De Shi Wei-Wei Wu De-Wei Li 

作者机构:Organ Transplant Center First Affiliated Hospital Zhejiang University School of Medicine Hangzhou 310003 China. wzjxdfpxy@*** 

出 版 物:《Hepatobiliary & Pancreatic Diseases International》 (国际肝胆胰疾病杂志(英文版))

年 卷 期:2004年第3卷第4期

页      面:511-515页

学科分类:1001[医学-基础医学(可授医学、理学学位)] 10[医学] 

基  金:This study was supported by grants from 973 National Key Project (2003CB515501 ) and the National Natural Science Foundation of China (No. 30270514) 

主  题:tissue-type plasminogen activator eukaryotic expression plasmid vascular endothelial cell organ transplantation 

摘      要:BACKGROUND: Tissue-type plasminogen activator(tPA), which is highly efficient and specific in resolution of thrombus, could significantly improve the survival rate and life-quality of the patients with thrombosis. This study was designed to clone human tPA gene, construct eukaryotic expression plasmid pcDNA3.1(+)/tPA, and evaluate their biological activities. METHODS: The tPA gene was obtained from dead human heart tissue with reverse transcriptase-polymerase chain reaction (RT-PCR). It was cloned to eukaryotic expression plasmid pcDNA3.1(+) by recombination strategy. The eukaryotic expression plasmid pcDNA3.1(+)/tPA was identified by restriction enzyme digestion and sequenced. The pcDNA3.1(+)/tPA was transfected into vascular smooth muscle cell (VSMC) by using lipofection. The tPA expression level was detected by Northern blot and dot blot, and the protein biological activities of tPA were detected by the fibrin plate technique. RESULTS: The tPA gene was cloned and pcDNA3.1(+)/tPA was constructed. The tPA expression levels of mRNA and protein were highly increased after pcDNA3.1(+)/tPA transfected into VSMC, and the expression of tPA protein showed evident biological activities. CONCLUSIONS: The present study has laid a foundation for further animal experiment in treating thrombus in transplanted organ by tPA gene transfection.

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