Skin repair using a porcine collagen I/III membrane--vascularization and epithelization properties

Dermatol Surg. 2010 Jun;36(6):919-30. doi: 10.1111/j.1524-4725.2010.01569.x.

Abstract

Background: Collagen membranes have been developed to overcome the problem of limited availability of skin grafts. Vascularization and restricted functional epithelization limit the success of bioartificial constructs.

Objective: To compare the vascularization, epithelization, and integration of a porcine collagen I/III membrane with that of split-thickness skin grafts on skin wounds.

Materials and methods: In 21 adult pigs, full-thickness skin defects on the rear side of the ear healed by split-thickness skin grafting, by covering with the membrane, or by free granulation. Skin samples on postoperative days 1, 3, 7, 14, 21, and 28 were evaluated histologically (hematoxylin-eosin, Sirius Red) and using immunohistochemistry (cytokeratin 5/6, transforming growth factor beta receptor (TGFbetaR-III) and immunoblot (TGFbeta(1,3), Smad2/3). Epithelial thickness and TGFbetaR-III-positive capillary area were quantitatively assessed.

Results: Epithelization and vascularization in the membrane group were not significantly different from in the group treated with a split-thickness skin graft. Free granulation showed significantly slower epithelization and vascularization (p<.05). TGFbeta(1) and Smad2/3 complex expression were high during free granulation. Matrix was distinguishable until day 7.

Conclusions: This membrane serves as a suitable full-thickness dermal substitute, because the membrane is vascularized faster than free granulation tissue and enables early epithelization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Collagen Type I / therapeutic use*
  • Collagen Type III / therapeutic use*
  • Dermis / blood supply
  • Dermis / injuries*
  • Dermis / pathology
  • Neovascularization, Physiologic / physiology
  • Skin, Artificial
  • Smad Proteins, Receptor-Regulated / metabolism
  • Swine
  • Tissue Scaffolds*
  • Transforming Growth Factor beta / metabolism
  • Wound Healing / physiology*
  • Wounds, Penetrating / metabolism
  • Wounds, Penetrating / pathology
  • Wounds, Penetrating / therapy*

Substances

  • Collagen Type I
  • Collagen Type III
  • Smad Proteins, Receptor-Regulated
  • Transforming Growth Factor beta