Volume 63, Issue 4 , Pages e364-e369, April 2010
The effect of growth hormone on fibroblast proliferation and keratinocyte migration
Summary
Background
The beneficial effects of growth hormones (GHs) on wound healing have been reported. Although the mechanism of how GH promotes wound healing is unclear, there are reports showing that the principal factor lies in the GH-stimulated production of IGF-1 in topical wounds. In this study, a human primary cell model was devised to examine how the topical application of GHs affects fibroblast proliferation and keratinocyte migration, which play fundamental roles in wound healing.
Methods
The fibroblasts were cultured in media with different concentrations of GH. The amount of fibroblast proliferation was assessed using a tetrazolium-based colourimetric assay (MTT assay). The amount of newly formed IGF-I mRNA was measured by reverse transcription and polymerase chain reaction (RT-PCR). Keratinocyte migration was compared using a migration assay.
Results
Fibroblast proliferation was significantly higher in the experimental group than in the control group (the absorbance of 2.5
IU L−1 GH applied group: 0.3954
±
0.056, control group: 0.2943
±
0.0554, P
<
0.05), and the promotion of IGF-I formation by fibroblasts was observed. There was more keratinocyte migration in the experimental group than in the control group (the remaining gap in the 2.5
IU L−1 GH applied group after keratinocyte migration: 46.57
±
2.22% of the primary gap, control group: 75.14
±
3.44%, P
<
0.05).
Conclusion
GH enhances the local formation of IGF-1, which activates fibroblast proliferation and keratinocyte migration. These results highlight the potential of the topical application of GHs in the treatment of wounds.
Keywords: Growth hormone, IGF-1, Fibroblast, Keratinocyte
To access this article, please choose from the options below
PII: S1748-6815(09)00752-9
doi:10.1016/j.bjps.2009.10.027
© 2009 British Association of Plastic, Reconstructive and Aesthetic Surgeons. All rights reserved.
Volume 63, Issue 4 , Pages e364-e369, April 2010
