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DOI: 10.1055/s-2007-1004060
© Georg Thieme Verlag KG Stuttgart · New York
Direct Gene Transfer into the Colon Using a Double-Balloon Catheter
Publication History
Publication Date:
17 March 2008 (online)
Abstract
Background and Study Aims: In spite of the many advances that have been made in understanding the molecular basis for diseases, a major obstacle to the treatment of human disorders remains the inability to express genes at specific sites in vivo. Recent progress in gene transfer technology has provided access to a variety of recombinant gene products that can be applied in clinical medicine for therapeutic purposes.
Materials and Methods: In an animal model, we describe here the way in which a marker gene can be introduced into the colon using a double-balloon catheter. Cationic liposomes were used as vehicles to introduce DNA into the living organism. RSV-LacZ plasmid coding for the enzyme β-galactosidase was used as a marker gene. Cells expressing β-galactosidase can be stained using the chromogen X-gal. Positive cells show a blue coloration in the cytoplasm.
Results: Both absorptive cells and goblet cells were successfully transduced with the marker gene. No evidence of similar staining was observed in control animals receiving a control plasmid or liposomes alone.
Conclusions: The method used is a simple, safe, and nontoxic way of delivering genes of interest to specific sites in the colon. Gene transfer may offer fresh potential for endoscopic interventions in colonic disease.