In Vivo Functionality of a Corneal Endothelium Transplanted by Cell-Injection Therapy in a Feline Model

Invest Ophthalmol Vis Sci. 2016 Apr;57(4):1620-34. doi: 10.1167/iovs.15-17625.

Abstract

Purpose: To evaluate the functionality of a corneal endothelium reconstituted by injection of corneal endothelial cells (CEC) in the anterior chamber of a feline model.

Methods: We operated the right eyes of 16 animals. Eight underwent central endothelial scraping and injection with 2 × 10(5) (n = 4) or 1 × 10(6) (n = 4) feline CEC supplemented with Y-27632 and labeled with 3,3'-Dioctadecyl-5,5'-Di(4-Sulfophenyl)Oxacarbocyanine (SP-DiOC18[3] or DiOC). After total endothelial scraping, two eyes were injected with 1 × 10(6) labeled CEC and Y-27632. The central (n = 3) or entire (n = 3) endothelium was scraped in six eyes followed by Y-27632 injection without CEC. Subjects were positioned eyes down for 3 hours. Outcomes included graft transparency, pachymetry, CEC morphometry, histology, electron microscopy, and function and wound healing-related protein immunostaining.

Results: Postoperatively, corneas grafted with 2 × 10(5) CEC and centrally scraped controls displayed the best transparency and pachymetry. Corneas grafted with 1 × 10(6) CEC yielded intermediate results. Entirely scraped controls remained hazy and thick. Histopathology revealed a confluent endothelial monolayer expressing sodium-potassium adenosine triphosphatase (Na(+)/K(+)-ATPase) and zonula occludens-1 (ZO-1) in corneas grafted with 2 × 10(5) CEC and centrally scraped controls, a nonuniform endothelial multilayer without expression of functional proteins in centrally scraped corneas grafted with 1 × 10(6) CEC, and a nonfunctional fibrotic endothelium in entirely scraped grafts and controls. Expression of DiOC in grafts was scarce.

Conclusions: Injected CEC contributed little to the incompletely functional endothelium of grafted corneas. Y-27632 injection without CEC following scraping reconstituted the healthiest endothelium. Further studies investigating the therapeutic effect of Y-27632 alone are needed to validate these conclusions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / pharmacology
  • Animals
  • Cats
  • Cell Count
  • Cell- and Tissue-Based Therapy*
  • Cells, Cultured
  • Corneal Pachymetry
  • Disease Models, Animal*
  • Endothelium, Corneal / physiology*
  • Endothelium, Corneal / transplantation*
  • Enzyme Inhibitors / pharmacology
  • Graft Survival / physiology
  • Injections, Intraocular
  • Microscopy, Electron
  • Pyridines / pharmacology
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Transplantation, Homologous
  • Wound Healing / physiology
  • Zonula Occludens-1 Protein / metabolism

Substances

  • Amides
  • Enzyme Inhibitors
  • Pyridines
  • Zonula Occludens-1 Protein
  • Y 27632
  • Sodium-Potassium-Exchanging ATPase