EXTRACELLULAR-MATRIX CHARACTERIZATION DURING HEALING OF FULL-THICKNESS WOUNDS TREATED WITH A COLLAGEN ELASTIN DERMAL SUBSTITUTE SHOWS IMPROVED SKIN REGENERATION IN PIGS/
En. Lamme et al., EXTRACELLULAR-MATRIX CHARACTERIZATION DURING HEALING OF FULL-THICKNESS WOUNDS TREATED WITH A COLLAGEN ELASTIN DERMAL SUBSTITUTE SHOWS IMPROVED SKIN REGENERATION IN PIGS/, The Journal of histochemistry and cytochemistry, 44(11), 1996, pp. 1311-1322
We investigated the architecture of the extracellular matrix (ECM) dur
ing healing of full-thickness wounds in the pig, Two different treatme
nts, one based on epidermal transplantation (split skin mesh grafts, S
P wounds) and one consisting of a combination of epidermal transplanta
tion and a dermal matrix substitute (MA wounds) were compared, The der
mal matrix consisted of native bovine collagen coated with elastin hyd
rolysate, The latter treatment reduced wound contraction and improved
tissue regeneration. The expression patterns of fibronectin, von Wille
brand factor, laminin, chondroitin sulfate, and elastin, detected by i
mmunohistochemistry, were examined in time and indicated different sta
ges of healing. During the early phase of healing the dermal matrix in
duced more granulation tissue, a different fibronectin expression patt
ern, and rapid vascular cell ingrowth (von Willebrand factor), Further
more, in the MA wounds chondroitin sulfate was detected earlier in the
basement membrane and fibronectin staining disappeared more rapidly,
During later stages of healing, chondroitin sulfate expression was sel
ective for areas in which ECM remodeling was active; in these specific
areas elastin staining reappeared. ECM remodeling and elastin regener
ation occurred both in the upper and lower dermis for the MA wounds bu
t only in the upper dermis for the SP wounds, Electron microscopic eva
luation of the wounds after 2 weeks showed many myofibroblasts in the
SP wounds, whereas in the MA wounds cells associated with the dermal m
atrix had characteristics of normal fibroblasts, The results suggest t
hat the biodegradable dermal matrix served as a template for dermal ti
ssue regeneration, allowed faster regeneration, and improved the quali
ty of healing in large full-thickness skin defects.