Immunolocalization and gene expression of matrilysin during corneal wound healing

Invest Ophthalmol Vis Sci. 1999 Jan;40(1):20-7.

Abstract

Purpose: To investigate the protein level of matrilysin and stromelysin-1 and the gene expression of matrilysin in rat corneas after excimer keratectomy using immunofluorescence staining, reverse transcriptase-polymerase Chain Reaction (RT-PCR), and in situ hybridization.

Methods: Rat corneas were treated with 3-mm excimer laser keratectomy (193-nm ArF). Unwounded corneas served as controls. Confocal microscopy was used to immunolocalize matrilysin protein at 6 hours, 1 day, 3 days, 1 week, 4 weeks, and 8 weeks after surgery. RT-PCR was performed to analyze matrilysin mRNA in unwounded controls and in 3-day wounded corneas. In situ hybridization was performed to localize matrilysin mRNA.

Results: Matrilysin was immunolocalized to the epithelial layers of unwounded and wounded corneas, predominantly to the leading edge at 6 hours and 1 day after wounding and to the epithelial layer at 3 to 7 days after surgery. Stromelysin-1 was expressed in the deep stromal layer in the first 3 days after wounding and in the area of newly synthesized stromal matrix 1 week after surgery. Upregulation of matrilysin expression 3 days after wounding was confirmed by RT-PCR. In situ hybridization revealed that the gene expression of matrilysin in rat corneas was upregulated during the migration phase (6 hours, 1 day) and that matrilysin mRNA was predominantly localized to the basal cell layers during the subsequent cell proliferation phase (7 and 14 days).

Conclusions: Basal epithelial cells express matrilysin during the migration proliferation phase of corneal wound healing after excimer keratectomy.

Publication types

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

MeSH terms

  • Animals
  • Cell Division
  • Cell Movement
  • Cornea / enzymology*
  • Cornea / surgery
  • Corneal Stroma / enzymology
  • Epithelium, Corneal / enzymology
  • Female
  • Gene Expression*
  • In Situ Hybridization
  • Lasers, Excimer
  • Matrix Metalloproteinase 3 / metabolism
  • Matrix Metalloproteinase 7
  • Metalloendopeptidases / genetics*
  • Metalloendopeptidases / metabolism*
  • Microscopy, Confocal
  • Photorefractive Keratectomy
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Up-Regulation
  • Wound Healing*

Substances

  • RNA, Messenger
  • Metalloendopeptidases
  • Matrix Metalloproteinase 3
  • Matrix Metalloproteinase 7