Expression of matrix metalloproteinases 2 and 9 in experimental corneal injury and fungal keratitis

Cornea. 2007 Jun;26(5):589-93. doi: 10.1097/ICO.0b013e318033b504.

Abstract

Purpose: Levels of matrix metalloproteinases (MMPs) can be modulated during corneal infection, but little is known about MMP profiles during fungal keratitis. The purpose of this study was to determine the effect of corneal trauma and immunosuppressive treatment on the expression kinetics of MMP-2 and MMP-9 during experimental keratomycosis.

Methods: Corneas of immunocompetent and cyclophosphamide-treated adult BALB/c mice were topically inoculated with 1 x 10 culturable units of Fusarium solani or mock-inoculated with or without superficial corneal scarification. Eyes were scored daily for disease severity and processed for zymography after 1.5 hours, 6 hours, 1 day, 4 days, or 8 days. Gelatinase activity was densitometrically quantitated and normalized to MMP-2 and MMP-9 controls.

Results: MMP-9 levels in nontraumatized eyes transiently increased at 6 hours after fungal exposure, but this increase was inhibited by cyclophosphamide treatment. Corneal injury significantly induced early MMP-9 expression that returned to baseline levels within 4 days. Cyclophosphamide pretreatment reduced and delayed MMP-9 after scarification. Fusarium exposure dampened the MMP-9 response to corneal trauma in immunocompetent and cyclophosphamide-treated animals. Ocular levels of MMP-2 were not affected by scarification, fungal exposure, or immunosuppressive treatment.

Conclusions: Ocular MMP-9 levels, but not MMP-2 levels, increased soon after corneal injury. A similar, although muted, MMP-9 response occurs during early filamentous fungal keratitis, with a kinetic profile similar to corneal disease progression. The early stage of ulcerative keratitis may involve selective regulation of corneal matrix metalloproteinases, suggesting an initial opportunity for therapeutic intervention.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Corneal Injuries*
  • Corneal Ulcer / drug therapy
  • Corneal Ulcer / enzymology*
  • Corneal Ulcer / microbiology
  • Cyclophosphamide / therapeutic use
  • Disease Models, Animal
  • Eye Infections, Fungal / drug therapy
  • Eye Infections, Fungal / enzymology
  • Eye Infections, Fungal / microbiology
  • Eye Injuries / drug therapy
  • Eye Injuries / enzymology*
  • Eye Injuries / microbiology
  • Female
  • Fusarium / growth & development
  • Fusarium / pathogenicity*
  • Immunosuppressive Agents / therapeutic use
  • Matrix Metalloproteinase 2 / metabolism*
  • Matrix Metalloproteinase 9 / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Mycoses / drug therapy
  • Mycoses / enzymology*
  • Mycoses / microbiology
  • Wounds, Nonpenetrating / drug therapy
  • Wounds, Nonpenetrating / enzymology
  • Wounds, Nonpenetrating / microbiology

Substances

  • Immunosuppressive Agents
  • Cyclophosphamide
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9