Morphological and immunohistochemical characteristics of the equine corneal epithelium

Vet Ophthalmol. 2019 Nov;22(6):778-790. doi: 10.1111/vop.12651. Epub 2019 Feb 14.

Abstract

Objective: The morphology of the corneal epithelium in two age groups of horses is described. Distribution patterns of proliferation-, differentiation-, stem cell-associated markers and cell junction proteins were assessed.

Methods: Corneal samples from 12 horses (six foals and six adult horses) were analyzed after H&E staining and immunohistochemistry using the following antibodies: E-cadherin, β-catenin, Connexin 43 (Cx43), tight junction protein 1 (TJP1), cytokeratin (CK) 14, CK 19, CK 3, CK 10, vimentin, Ki67, p63, nerve growth factor (NGF), ABCG2, and epithelial growth factor receptor. Semiquantitative analysis of crypt, limbal, peripheral, and central zone was performed. Semithin and ultrathin sections were used for ultrastructural evaluation of the epithelium.

Results: The height of the epithelium varied between age groups and crypts were consistently present. In the peripheral and central epithelium, three types of basal cells resembling a pseudostratified epithelium were characterized. Potential stem cell markers (CK 14, p63, NGF, and ABCG2) were present in all zones with decreasing frequency toward the center. Cornea-specific differentiation marker CK 3 was not expressed in the most basal cell layer of the limbal epithelium. E-cadherin, β-catenin, and Cx43 revealed a similar apico-lateral signal pattern throughout the entire epithelium; only TJP1 was additionally seen at the basal surface.

Conclusions: This study presents a systematic semiquantitative evaluation of the equine corneal epithelium, showing the presence of crypts as potential stem cell niche with CK 14, p63, NGF, and ABCG2 as relevant markers for cells with regenerative capacity. The pseudostratified arrangement of the basal layer was a unique finding.

Keywords: cell junction proteins; corneal stem cell niche; crypt; horse; limbus; semiquantitative evaluation.

MeSH terms

  • Aging
  • Animals
  • Antibodies / immunology
  • Epithelial Cells / physiology*
  • Epithelium, Corneal / anatomy & histology*
  • Epithelium, Corneal / chemistry*
  • Epithelium, Corneal / cytology
  • Gene Expression Regulation / physiology
  • Horses / anatomy & histology*
  • Immunohistochemistry / veterinary*
  • Stem Cells / physiology

Substances

  • Antibodies