Hepatocyte growth factor; expression, concentration and biological activity in chronic leg ulcers

J Dermatol Sci. 2005 Feb;37(2):75-85. doi: 10.1016/j.jdermsci.2004.11.002. Epub 2004 Dec 28.

Abstract

Background: Hepatocyte growth factor (HGF) is a multifunctional cytokine that is involved in recovery process after organ injuries.

Objective: We studied HGF and the membrane bound receptor, c-met locally in patients who suffered from chronic leg ulcers (> or =1 year) caused by venous insufficiency.

Methods: Skin biopsies from the edge of the ulcers were taken from patients (n=13) and studied by immunohistochemical staining for detection of HGF and c-met. Skin biopsies from healthy volunteers (n=10) were used as the control material. Ulcer secretion from chronic ulcers (n=11) was examined for the presence of HGF by ELISA and the concentration of HGF was compared with acute ulcers in healthy controls (n=10) and in patients operated for a non-invasive breast cancer (n=12).

Results: We observed that c-met expression in the ulcer area increased significantly in chronic ulcers compared to controls (p=0.005). Concentration of ulcer-HGF in the patients with chronic ulcer was significantly higher than acute ulcers (p<0.01). The biological activity of HGF in ulcer secret was assessed in-vitro in transferred, mouse skin epithelial cell monolayer. Enhanced migration and morphologic changes were seen after adding ulcer secret from acute ulcers (> 1 ng/mL) that was inhibited by anti-HGF antibodies. No biological activity was observed by adding ulcer secret from chronic ulcers irrespective HGF concentration.

Conclusion: We conclude that in chronic skin ulcers decreased biological activity of endogenous HGF and overexpression of c-met is seen which might explain fibrosis and delayed recovery. Administration of exogenous active HGF might contribute to accelerated healing in these patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Biopsy
  • Blotting, Western
  • Breast Neoplasms / metabolism
  • Case-Control Studies
  • Cell Line
  • Cell Movement
  • Cytokines / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Epithelial Cells / cytology
  • Female
  • Hepatocyte Growth Factor / biosynthesis*
  • Hepatocyte Growth Factor / physiology*
  • Humans
  • Immunohistochemistry
  • Leg Ulcer / metabolism*
  • Male
  • Mice
  • Proto-Oncogene Proteins c-met / biosynthesis*
  • Skin / pathology*
  • Time Factors
  • Transforming Growth Factor beta / metabolism
  • Transforming Growth Factor beta1
  • Ulcer / metabolism
  • Venous Insufficiency / pathology
  • Wound Healing

Substances

  • Cytokines
  • TGFB1 protein, human
  • Tgfb1 protein, mouse
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • Hepatocyte Growth Factor
  • Proto-Oncogene Proteins c-met