Development of an epithelium-specific expression cassette with human DNA regulatory elements for transgene expression in lung airways

被引:60
作者
Chow, YH
O'Brodovich, H
Plumb, J
Wen, YX
Sohn, KJ
Lu, Z
Zhang, FY
Lukacs, GL
Tanswell, AK
Hui, CC
Buchwald, M
Hu, J
机构
[1] Hosp Sick Children, Div Resp Res, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Lung Gene Therapy Programme, Toronto, ON M5G 1X8, Canada
[3] Hosp Sick Children, Div Neonatol, Toronto, ON M5G 1X8, Canada
[4] Hosp Sick Children, Div Endocrinol, Toronto, ON M5G 1X8, Canada
[5] Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, Canada
[6] Univ Toronto, MRC, Grp Lung Dev, Toronto, ON M5G 1X8, Canada
[7] Univ Toronto, Dept Paediat, Toronto, ON M5G 1X8, Canada
[8] Univ Toronto, Dept Clin Biochem, Toronto, ON M5G 1X8, Canada
[9] Univ Toronto, Dept Med Genet, Toronto, ON M5G 1X8, Canada
基金
英国惠康基金;
关键词
cystic fibrosis transmembrane conductance regulator; transgenic mice; intron enhancer; cell specificity; secreted alkaline phosphatase;
D O I
10.1073/pnas.94.26.14695
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The efficient expression of therapeutic genes in target cells or tissues is an important component of efficient and safe gene therapy. Utilizing regulatory elements from the human cytokeratin 18 (K18) gene, including 5' genomic sequences and one of its introns, we have developed a novel expression cassette that can efficiently express reporter genes, as well as the human cystic fibrosis transmembrane conductance regulator (CFTR) gene, in cultured lung epithelial cells. CFTR transcripts expressed from the native K18 enhancer/promoter include two alternative splicing products, due to the activation of two cryptic splice sites in the CFTR coding region. Modification of the K18 intron and CPTR cDNA sequences eliminated the cryptic splice sites without changing the CFTR amino acid sequence, and led to enhanced CFTR mRNA and protein expression as well as biological function. Transgenic expression analysis in mice showed that the modified expression cassette can direct efficient and epithelium-specific expression of the Escherichia coli LacZ gene in the airways of fetal lungs, with no detectable expression in lung fibroblasts or endothelial cells, This is the first expression cassette which selectively directs lung transgene expression for CFTR gene therapy to airway epithelia.
引用
收藏
页码:14695 / 14700
页数:6
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