Comparison of EGF with VEGF Non-Viral Gene Therapy for Cutaneous Wound Healing of Streptozotocin Diabetic Mice.
10.4093/dmj.2011.35.3.226
- Author:
Junghae KO
1
;
Haejung JUN
;
Hyesook CHUNG
;
Changshin YOON
;
Taekyoon KIM
;
Minjeong KWON
;
Soonhee LEE
;
Soojin JUNG
;
Mikyung KIM
;
Jeong Hyun PARK
Author Information
1. Molecular Therapy Laboratory, Paik Memorial Institute for Clinical Research, Busan, Korea. pjhdoc@chol.com
- Publication Type:Original Article
- Keywords:
Epidermal growth factor;
Gene therapy;
Non-viral;
Skin wound;
Vascular endothelial growth factor
- MeSH:
Animals;
DNA;
Epidermal Growth Factor;
Genetic Therapy;
Half-Life;
Intercellular Signaling Peptides and Proteins;
Laser-Doppler Flowmetry;
Mice;
Phospholipids;
Skin;
Streptozocin;
Sulfur Hexafluoride;
Vascular Endothelial Growth Factor A;
Wound Healing
- From:Diabetes & Metabolism Journal
2011;35(3):226-235
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: To accelerate the healing of diabetic wounds, various kinds of growth factors have been employed. It is the short half-life of administered growth factors in hostile wound beds that have limited wide-spread clinical usage. To overcome this limitation, growth factor gene therapy could be an attractive alternative rather than direct application of factors onto the wound beds. We administered two growth factor DNAs, epidermal growth factor (EGF) and vascular endothelial growth factor (VEGF) into a cutaneous wound on diabetic mice. We compared the different characteristics of the healing wounds. METHODS: Streptozotocin was injected intraperitoneally to induce diabetes into C57BL/6J mice. The ultrasound micro-bubble destruction method with SonoVue as a bubbling agent was used for non-viral gene delivery of EGF828 and VEGF165 DNAs. Each gene was modified for increasing efficacy as FRM-EGF828 or minicircle VEGF165. The degree of neoangiogenesis was assessed using qualitative laser Doppler flowmetry. We compared wound size and histological findings of the skin wounds in each group. RESULTS: In both groups, accelerated wound closure was observed in the mice receiving gene therapy compared with non treated diabetic control mice. Blood flow detected by laser doppler flowmetry was better in the VEGF group than in the EGF group. Wound healing rates and histological findings were more accelerated in the EGF gene therapy group than the VEGF group, but were not statistically significant. CONCLUSION: Both non-viral EGF and VEGF gene therapy administrations could improve the speed and quality of skin wound healing. However, the detailed histological characteristics of the healing wounds were different.
