Y. Okada et al., IMMUNOLOCALIZATION OF PROTOONCOGENE PRODUCTS IN KERATOCYTES AFTER EPITHELIAL ABLATION, ALKALI BURN AND PENETRATING INJURY OF THE CORNEA IN RATS, Graefe's archive for clinical and experimental ophthalmology, 236(11), 1998, pp. 853-858
Background: We examined the immunolocalization of proto-oncogene produ
cts, including c-Fos and c-Jun, in the rat cornea during epithelial an
d stromal wound healing after simple epithelial ablation, penetrating
injury or alkali burn. Methods: Eighty-four male Wistar rats were divi
ded into three groups and subjected to treatments as follows: (a) abla
tion of central corneal epithelium leaving basement membrane intact, (
b) alkali burn in the central cornea with 1 N NaOH and (c) penetrating
injury at the central cornea. The affected eyes were then enucleated
after various intervals of healing. The frozen sections were immunohis
tochemically stained with the antibodies against proto-oncogene produc
ts. Results: c-Fos- and c-Jun-immunoreactive cells were detected in th
e epithelium around the epithelial defect from 60 to 120 min after the
se treatments. The distribution of these cells were varied in these th
ree types of injury. The immunoreactivities for these proteins were al
so detected in keratocytes after epithelial ablation. In the corneas w
ith alkali burn, the immunoreactivities were detected in the keratocyt
es in the whole corneal stroma, and these immunoreactions were stronge
r than those observed in simple epithelial ablation. In the corneas wi
th penetrating injury, such immunoreaction was seen only in keratocyte
s around the wound. Conclusion: These findings indicate that activator
protein 1-mediated transcriptional activation for epithelial migratio
n is initiated in the early phase after each injury, and that stromal
keratocytes are also transcriptionally activated not only by alkali bu
rn or penetrating injury but also by simple epithelial ablation in whi
ch basement membrane was not affected.