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  • Absence of scar formation in human donor cornea with prior laser in situ keratomileusis.

Absence of scar formation in human donor cornea with prior laser in situ keratomileusis.

Journal of cataract and refractive surgery (2005-08-18)
Siegfried G Priglinger, Christian-Albrecht May, Claudia S Alge, Armin Wolf, Aljoscha S Neubauer, Anselm Kampik, Ulrich Welge-Luessen
ABSTRACT

To investigate transglutaminases (enzymes capable of cross-linking extracellular matrix proteins to proteolysis-resistant complexes during scar tissue formation) in a human donor cornea after successful laser in situ keratomileusis (LASIK) without clinical complications and to compare with the results in a human donor cornea with corneal scarring after corneal injury. Department of Ophthalmology, Ludwig-Maximilians University, Munich, Germany. A donor cornea with prior uneventful LASIK treatment and 1 with corneal scarring after penetrating injury were investigated. Cryostat sections were stained immunohistochemically for tissue transglutaminase (tTG), keratocyte transglutaminase (kTG), and their reaction product epsilon-(gamma-glutamyl)-lysine. With light microscopy, the flap interface of the LASIK-treated eye could hardly be detected, while in the injured eye, infiltration of cells and a clear margin next to the scar formation were present. Immunohistochemistry demonstrated a distinct staining for tTG, kTG, and epsilon-(gamma-glutamyl)-lysine in the corneal scar. In contrast, neither transglutaminase nor epsilon-(gamma-glutamyl)-lysine staining could be observed at the flap margin or in the interface of the LASIK-treated donor eye. Irreversible protein cross-linking of transglutaminases via epsilon-(gamma-glutamyl)-lysine connections seem to be indicators for scarring in corneal wound healing. The absence of transglutaminases and their reaction product epsilon-(gamma-glutamyl)-lysine in a LASIK-treated cornea supports the idea of missing scar tissue formation after LASIK surgery.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
γ-Glu-ε-Lys