Acceleration of wound healing by combined gene transfer of hepatocyte growth factor and prostacyclin synthase with Shima Jet
Open Access
- 30 March 2006
- journal article
- research article
- Published by Springer Nature in Gene Therapy
- Vol. 13 (15) , 1143-1152
- https://doi.org/10.1038/sj.gt.3302767
Abstract
Although skin diseases are one of the target diseases for gene therapy, there has been no practical gene transfer method. First, we examined gene transfer efficiency of the spring-powered jet injector, Shima Jet, which was originally developed as a non-needle jet injector of insulin. Local gene expression was about 100 times higher when the luciferase plasmid was transferred by the Shima Jet than by a needle. Gene transfer of beta-galactosidase revealed gene expression in the epidermis. Based on these results, we then examined the potential of gene therapy using the Shima Jet for wound healing. An increase of cellular proliferation of the epidermis and the number of microvessels in the granulation tissue was observed after hepatocyte growth factor (HGF) gene transfer. An increase in blood flow around the wound was observed after prostacyclin synthase (PGIS) gene transfer. Moreover, promotion on wound healing was observed in HGF gene transferred group, and further promotion was observed in combined gene transferred group as assessed by measuring wound area. These results indicate that co-transfer of HGF and PGIS genes by the Shima Jet could be an effective strategy to wound healing.Keywords
This publication has 39 references indexed in Scilit:
- Electroporative transfection with KGF-1 DNA improves wound healing in a diabetic mouse modelGene Therapy, 2004
- DNA electrotransfer: its principles and an updated review of its therapeutic applicationsGene Therapy, 2004
- Gene Transfer of Human Hepatocyte Growth Factor into Rat Skin Wounds Mediated by Liposomes Coated with the Sendai Virus (Hemagglutinating Virus of Japan)The American Journal of Pathology, 2002
- The Majority of Keratinocytes Incorporate Intradermally Injected Plasmid DNA Regardless of Size but Only a Small Proportion of Cells Can Express the Gene ProductJournal of Investigative Dermatology, 2002
- Enhanced delivery of naked DNA to the skin by non-invasive in vivo electroporationBiochimica et Biophysica Acta (BBA) - General Subjects, 2002
- Recombinant AAV vector encoding human VEGF165 enhances wound healingGene Therapy, 2002
- Targeted gene delivery to skin cells in vivo: A comparative study of liposomes and polymers as delivery vehiclesJournal of Pharmaceutical Sciences, 2002
- In Vivo Assessment of Gene Delivery to Keratinocytes by Lentiviral VectorsJournal of Virology, 2002
- Safety and Pharmacokinetics of Naked Plasmid DNA in the Skin: Studies on Dissemination and Ectopic Expression11Presented in part at the 28th Annual Meeting of the European Society for Dermatological Research, Montpellier, France, September 22–25, 1999.Journal of Investigative Dermatology, 2001
- Boosting epidermal growth factor receptor expression by gene gun transfection stimulates epidermal growth in vivoWound Repair and Regeneration, 2000