Lack of keratinocyte growth factor retards angiogenesis in cutaneous wounds
1Department of Burns and Plastic Surgery, The Third Xiangya Hospital of Central South University, Changsha, Hunan, China.
Abstract:
This study investigated the effects of keratinocyte growth factor (KGF) on wound healing. Full-thickness excisional dorsal wounds were created on KGF knockout mice (KGF KO, n = 12) and wild-type C57BL/6 mice (WT, n = 12), and wound closure rates were measured. Immunohistochemical staining was used to investigate cell proliferation and blood vessel density by assessing Ki67 and CD31 protein levels, respectively, and real-time reverse transcription-polymerase chain reaction was used to measure vascular endothelial growth factor (VEGF) mRNA levels. No differences in the rate of wound closure were found between KGF KO and WT mice, however the KGF KO mice showed decreased proliferation of keratinocytes, angiogenesis and VEGF mRNA levels in vivo. These results suggest that KGF may play an important role in the regulation of VEGF gene expression and angiogenesis during wound healing.
Insights
Keratinocyte growth factor (KGF) is crucial for wound healing, regulating angiogenesis and cell proliferation. While KGF knockout mice showed no difference in wound closure, they exhibited reduced angiogenesis and VEGF levels.
Area of Science:
- Wound healing research
- Molecular biology
- Dermatology
Background:
- Keratinocyte growth factor (KGF) is a key regulator of epithelial cell growth and differentiation.
- Understanding KGF's role in wound healing is essential for developing new therapeutic strategies.
Purpose of the Study:
- To investigate the specific effects of KGF on the processes involved in wound healing.
- To determine the impact of KGF deficiency on keratinocyte proliferation, angiogenesis, and vascular endothelial growth factor (VEGF) expression during wound repair.
Main Methods:
- Creation of full-thickness excisional dorsal wounds in KGF knockout (KGF KO) and wild-type (WT) mice.
- Measurement of wound closure rates.
- Immunohistochemical analysis for Ki67 (proliferation) and CD31 (angiogenesis).
- Real-time reverse transcription-polymerase chain reaction (RT-PCR) for VEGF mRNA levels.
Main Results:
- No significant difference in the overall rate of wound closure was observed between KGF KO and WT mice.
- KGF KO mice exhibited significantly decreased keratinocyte proliferation compared to WT mice.
- Reduced angiogenesis and lower VEGF mRNA levels were detected in KGF KO mice.
- These findings indicate an impaired wound healing microenvironment in the absence of KGF.
Conclusions:
- KGF plays a critical role in regulating keratinocyte proliferation and angiogenesis during wound healing.
- KGF influences VEGF gene expression, impacting the formation of new blood vessels.
- Despite no impact on closure rate, KGF is vital for the molecular and cellular processes underlying effective wound repair.
Related Concept Videos
Regulation of Angiogenesis and Blood Supply
Mechanism of Angiogenesis
Mitogens and the Cell Cycle
Renewal of Skin Epidermal Stem Cells
Clinical Applications of Epidermal Stem Cells
Phases of Wound Repair
Formation of Blood Clot
In case of deep injuries, trauma to blood vessels results in blood loss. In the meantime, phospholipids released from the ruptured endothelial cellular membrane are converted into arachidonic...


