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Human CMV immediate‐early enhancer: a useful tool to enhance cell‐type‐specific expression from lentiviral vectors
Author(s) -
Gruh Ina,
Wunderlich Stephanie,
Winkler Monica,
Schwanke Kristin,
Heinke Jennifer,
Blömer Ulrike,
Ruhparwar Arjang,
Rohde Bettina,
Li RenKe,
Haverich Axel,
Martin Ulrich
Publication year - 2008
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.1122
Subject(s) - enhancer , biology , viral vector , reporter gene , human cytomegalovirus , transduction (biophysics) , transgene , gene expression , microbiology and biotechnology , green fluorescent protein , genetic enhancement , gene , genetics , biochemistry , recombinant dna
Background Lentiviral vectors are attractive delivery tools for gene therapy, especially in terminally differentiated target cells. While restriction of gene expression to specific cell populations is of particular importance, highly efficient cell‐type‐specific gene expression after viral gene transfer so far has been hampered by low levels of transgene expression. Methods Addressing this problem, we have integrated the human cytomegalovirus (CMV) immediate‐early enhancer into an ‘advanced’ generation lentiviral vector. Expression cassettes with the reporter gene green fluorescent protein (GFP), combined with the woodchuck hepatitis virus posttranscriptional regulatory element (WPRE) under control of a ubiquitous phosphoglycerate kinase (mouse PGK), cardiomyocyte‐ (human atrial natriuretic factor (ANF), human ventricular myosin light chain (MLC2v)), or type II alveolar epithelial cell (AT‐2)‐specific human surfactant protein C (SP‐C) promoter, were introduced. As insertion of an enhancing element can interfere with the promoter's specificity, expression levels conferred by our enhancer/promoter constructs were evaluated in target and non‐target cells. Results Transduction of target cells with human CMV enhancer containing lentiviral vectors resulted in a multiple‐log increase in GFP expression compared to corresponding vectors lacking the human CMV enhancer. In the case of the ANF, the MLC2v, and the SP‐C promoters, tissue‐specific reporter gene expression in cardiomyocytes and in lung AT‐2 cells was maintained, as expression in non‐target cells increased only up to 7‐fold. Conclusions The results of this study indicate that lentiviral vectors with the human CMV enhancer conferring efficient cell‐type‐specific gene expression may be useful tools for gene therapy purposes or cell tracing, e.g. to analyze stem cell differentiation in transplantation and co‐culture settings. Copyright © 2007 John Wiley & Sons, Ltd.