Metalloproteinase activation cascade after burn injury: a longitudinal analysis of the human wound environment

J Invest Dermatol. 1994 Nov;103(5):660-4. doi: 10.1111/1523-1747.ep12398424.

Abstract

In this paper, we present a longitudinal study on metalloproteinases in wound-fluid samples collected from three patients with partial- to full-thickness burn wounds. Gelatin zymography showed that 92-kDa gelatinase (MMP-9) and its 225-kDa complex could be detected in burn fluid beginning as early as 4-8 h after injury. Marked increases in MMP-9 levels as well as activation of the proenzyme occurred between day 0 and day 2. The 72-kDa gelatinase (MMP-2) proenzyme was not detected until day 2 and activated enzyme did not appear until day 4. Stromelysin (MMP-3), both proenzyme and activated-enzyme forms, was first observed on day 4. Fluid-phase proteinase activity detected by azocoll degradation roughly corresponded with the level of stromelysin rather than the gelatinases. Our results provide evidence for a regulated metalloproteinase activation cascade following acute traumatic injury and demonstrate in vivo expression of metalloproteinase activity.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Azo Compounds / metabolism
  • Body Fluids / metabolism
  • Burns / metabolism*
  • Collagen / metabolism
  • Coloring Agents
  • Enzyme Activation
  • Female
  • Humans
  • Longitudinal Studies
  • Male
  • Matrix Metalloproteinase 3
  • Metalloendopeptidases / metabolism*
  • Middle Aged

Substances

  • Azo Compounds
  • Coloring Agents
  • Azocoll
  • Collagen
  • Metalloendopeptidases
  • Matrix Metalloproteinase 3