FGF2 |
Reepithelialization and granulation tissue formation |
Global deletion of FGF2 in mice cause delayed skin wound healing [16]. |
FGF2 application stimulates human keratinocytes migration in vitro [88]. |
TGF-β
|
Inflammation |
Global deletion of TGF-β in mice cause delayed wound healing [12]; TGF-β application in rats at the wound site accelerates wound healing [14, 53]. |
TGF-β application stimulates keratinocyte migration in skin explants by upregulating the expression of integrins [51, 52]. |
Reepithelialization |
Keratinocytes migration |
Granulation tissue formation |
VEGF-A |
Angiogenesis |
Keratinocyte-specific deletion of VEGF-A in mice reduces blood vessel formation at the wound site [74]. Topical VEGF in diabetic mice accelerate wound healing [74]. |
VEGF-A stimulates endothelial cells in vitro to increase tube formation [74]. |
HB-EGF |
Reepithelialization |
Keratinocyte-specific HB-EGF-deficient mice have delayed migration and wound closure [89]. |
HB-EGF overexpression by epidermal keratinocytes increases motility [90]. |