Elsevier

Experimental Eye Research

Volume 69, Issue 5, November 1999, Pages 475-481
Experimental Eye Research

Regular article
Keratocyte Apoptosis Associated with Keratoconus

https://doi.org/10.1006/exer.1999.0719Get rights and content

Abstract

Keratoconus is an ectatic corneal dystrophy associated with stromal thinning and disruption of Bowman's layer. The purpose of this study was to explore a possible association between keratocyte apoptosis and keratoconus. Keratocyte apoptosis was evaluated in corneas of patients with keratoconus, corneas of patients with stromal dystrophies, and normal donor corneas using the transferase-mediated dUTP-digoxigenin nick and labeling (TUNEL) assay. Keratocyte apoptosis was also studied in keratoconus and normal corneas using transmission electron microscopy. TUNEL-stained keratocytes were detected in 60% of corneas with keratoconus, but only 35% of corneas with stromal dystrophies (P =0.03). The number of TUNEL-positive keratocytes detected in the keratoconus, stromal dystrophy, and normal corneas was 7±1 (mean±standard error, range 0–20), 2±0.8 (range 0–9), and 0±0 (range 0–0) TUNEL-positive cells per section, respectively. The differences between the keratoconus and the stromal dystrophy (P =0.0097) or the normal cornea (P =0.01) groups were statistically significant. The difference between the stromal dystrophy and normal cornea groups was not statistically significant (P =0.45). The stromal dystrophy group was included to account for surgery-associated keratocyte apoptosis. No TUNEL-stained keratocytes were detected in normal corneas. Cell morphologic changes consistent with apoptosis were detected by transmission electron microscopy (TEM) in keratocytes of keratoconus corneas, but not in keratocytes in normal corneas. Chronic keratocyte apoptosis associated with ongoing epithelial injury may link risk factors associated with keratoconus such as chronic eye rubbing, contact lens wear, or atopic eye disease. Similarly, increases that have been detected in several different degradative enzymes in keratoconus corneas could be associated with chronic keratocyte apoptosis and less than perfect control of release of intracellular contents.

References (28)

  • M. Campos et al.

    Keratocyte loss after corneal deepithelialization in primates and rabbits

    Arch. Ophthalmol.

    (1994)
  • J.T. Coyle

    Keratoconus and eye rubbing

    Am. J. Ophthalmol.

    (1984)
  • E.J. Fabre et al.

    Binding sites for human interleukin-1 alpha, gamma interferon and tumor necrosis factor on cultured fibroblasts of normal cornea and keratoconus

    Curr. Eye Res.

    (1991)
  • M.E. Fini et al.

    Collagenolytic/gelatinolytic metalloproteinases in normal and keratoconus corneas

    Curr. Eye Res.

    (1992)
  • Cited by (0)

    f1

    Address correspondence to: Steven E. Wilson, Department of Ophthalmology, University of Washington School of Medicine, Box 356485, Seattle, WA 99195-6485, U.S.A.

    View full text