Spatial and temporal control of transgene expressionin vivo using a heat-sensitive promoter and MRI-guided focused ultrasound
Autor: | C. Maurange, C.T.W. Moonen, H. de Verneuil, P. Smirnov, A. Vekris, J. A. de Zwart, Véronique Bouchaud, Rares-Vasile Salomir, E. Guilhon, Pierre Voisin, Paul Canioni, Bruno Quesson |
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Rok vydání: | 2003 |
Předmět: |
Hyperthermia
Hot Temperature Time Factors Transgene Biology Marker gene Green fluorescent protein Mice In vivo Drug Discovery Gene expression Tumor Cells Cultured Genetics medicine Animals Humans HSP70 Heat-Shock Proteins Transgenes Viability assay Rats Wistar Promoter Regions Genetic Molecular Biology Genetics (clinical) Ultrasonography Regulation of gene expression Neoplasms Connective Tissue Glioma Hyperthermia Induced medicine.disease Magnetic Resonance Imaging Molecular biology Mice Mutant Strains Rats Gene Expression Regulation Molecular Medicine Heat-Shock Response |
Zdroj: | The Journal of Gene Medicine. 5:333-342 |
ISSN: | 1521-2254 1099-498X |
DOI: | 10.1002/jgm.345 |
Popis: | Background Among the techniques used to induce and control gene expression, a non-invasive, physical approach based on local heat in combination with a heat-sensitive promoter represents a promising alternative but requires accurate temperature control in vivo. MRI-guided focused ultrasound (MRI-FUS) with real-time feedback control allows automatic execution of a predefined temperature-time trajectory. The purpose of this study was to demonstrate temporal and spatial control of transgene expression based on a well-defined local hyperthermia generated by MRI-FUS. Methods Expression of the green fluorescent protein (GFP) marker gene was used. Two cell lines were derived from C6 glioma cells. The GFP expression of the first one is under the control of the CMV promoter, whereas it is under the control of the HSP70 promoter in the second one and thus inducible by heat. Subcutaneous tumours were generated by injection in immuno-deficient mice and rats. Tumours were subjected to temperatures varying from 42 to 50 °C for 3 to 25 min controlled by MRI-FUS and analyzed 24 h after the heat-shock. Endogenous HSP70 expression and C6 cell distribution were also analyzed. Results The results demonstrate strong expression at 50 °C applied during a short time period (3 min) without affecting cell viability. Induced expression was also clearly shown for temperature in the range 44–48 °C but not at 42 °C. Conclusions Heating with MRI-FUS allows a tight and non-invasive control of transgene expression in a tumour. Copyright © 2002 John Wiley & Sons, Ltd. |
Databáze: | OpenAIRE |
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