转染
间充质干细胞
分子生物学
遗传增强
因子IX
组织因子
免疫印迹
互补DNA
细胞培养
抗体
逆转录病毒
干细胞
病毒学
生物
免疫学
医学
基因
病毒
凝结
内科学
细胞生物学
遗传学
作者
Zhenping Chen,Chunlan Dong,Xiaoming Feng,Zhenping Chen,Zeping Zhou,Xianhui Xu,Qinjun Zhao,Zhiyong Qiu,Qian Ren,Lei Zhang,Zhongchao Han
出处
期刊:PubMed
[National Institutes of Health]
日期:2009-02-01
卷期号:17 (1): 184-7
被引量:2
摘要
The purpose of this study was to investigate the expression of human Factor IX (hFIX) in retrovirus-transfected human umbilical cord tissue derived mesenchymal stem cells (hUCT-MSCs). The pLEGFP-N1-hFIX vector was generated by cloning a 3.0 kb Bgl II-BamH I fragment from the pIRES2-EGFP-hFIX plasmid containing the hFIX cDNA and part of intron 1 of hFIX in pLEGFP-N1 vector. The retroviral supernatants were produced from the Phoenix packaging cell line and then infected the hUCT-MSCs. After selection with G418 for 10 day, the expression of FIX was detected by ELISA and Western blot. The biological activity of FIX was determined by the clotting assay employing human Factor IX-deficient plasma. The results showed that compared with the activity of pooled human normal plasma (100%), transduced cells produced biologically active hFIX with 100-130% activity in two-day culture supernatant and expressed hFIX at levels of 2.68 +/- 0.36 microg/10(6) cells/24 hours after G418 selection for 10 days. The secretion of hFIX into culture supernatant was also confirmed by Western blot analysis. It is concluded that genetically modified hUCT-MSCs can express biologically active hFIX and thus serve as an efficient drug delivery vehicle carrying hFIX used as a way of somatic gene therapy for hemophilia B.
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