Purpose: Epithelial migration is essential for healing of the ablated corne
al epithelium. To reveal the mechanism which enables the corneal epithelial
cells to dissociate during migration, we investigated the immunolocalizati
on of the components of the desmosome, which is the main constituent of the
intercellular junction attaching the intermediate filaments to the cell su
rface, desmoplakin 1, desmoglein and plakoglobin, in the corneal epithelium
during wound healing in rats. Methods: Under general anesthesia with ether
inhalation, Wistar rats (n = 48) underwent removal of the central corneal
epithelium of one eye with a small trephine and a sealpel. After various in
tervals of healing (5 min; 1,3, 6, 9, 12, 24, 48 h; 1 and 2 weeks), the ani
mals were killed and the affected eye was excised. Cryosections of each ant
erior segment of the eye were fixed with cold acetone and treated with prim
ary antibodies against desmoplakin 1, desmoglein and plakoglobin. Immunoloc
alization of these substances was visualized by the peroxidase-diaminobenzi
dine reaction. Results: A marked immunoreactivity for these desomosome comp
onents was detected at the intercellular junction in the normal corneal and
conjunctival epithelium. At 6-24 h after epithelial ablation, a weak immun
oreactivity for desmoplakin 1 and plakoglobin was observed in the migrating
epithelium. At 48 h after epithelial ablation, a marked immunoreactivity f
or these desmosome components was seen again. At 6-48 h after epithelial ab
lation, a weak immunoreactivity for desmoglein was observed in the migratin
g epithelium. At 1 week after epithelial ablation, a marked immunoreactivit
y for this desmosome component reappeared. The regenerated epithelium gradu
ally exhibited normal immunolocalization of the proteins. Conclusions: The
desmosome components were considered to be degraded or destroyed prior to e
pithelial migration and reconstructed during healing of the squamous epithe
lium. Copyright (C) 2001 S. Karger AG,Basel.