Comparison of the rabbit and human corneal endothelial proteomes regarding proliferative capacity

Exp Eye Res. 2021 Aug:209:108629. doi: 10.1016/j.exer.2021.108629. Epub 2021 May 23.

Abstract

The shortage of human donor corneas has raised important concerns about engineering of corneal endothelial cells (CECs) for clinical use. However, due to the limited proliferative capacity of human CECs, driving them into proliferation and regeneration may be difficult. Unlike human CECs, rabbit CECs have a marked proliferative capacity. To clarify the potential reason for this difference, we analysed the proteomes of four human corneal endothelium samples and four rabbit corneal endothelium samples with quantitative label-free proteomics and downstream analysis. We discovered that vitamin and selenocompound metabolism and some signaling pathways such as NF-kappa B signaling pathway differed between the samples. Moreover, TGFβ, PITX2 and keratocan were distinctively expressed in rabbit samples, which might be associated with active proliferation in rabbit CECs. This study illustrates the proteomic differences between human and rabbit CECs and might promote CEC engineering strategies.

Keywords: Corneal endothelium; Proliferative capacity; Proteomics.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • Cell Differentiation
  • Cells, Cultured
  • Corneal Diseases / metabolism*
  • Corneal Diseases / pathology
  • Corneal Diseases / surgery
  • Corneal Transplantation / methods*
  • Disease Models, Animal
  • Endothelium, Corneal / cytology
  • Endothelium, Corneal / metabolism*
  • Endothelium, Corneal / transplantation
  • Homeobox Protein PITX2
  • Homeodomain Proteins / biosynthesis*
  • Humans
  • Male
  • Middle Aged
  • Proteome / metabolism*
  • Proteomics / methods*
  • Rabbits
  • Tissue Preservation / methods
  • Transcription Factors / biosynthesis*
  • Transforming Growth Factor beta / biosynthesis*

Substances

  • Homeodomain Proteins
  • Proteome
  • Transcription Factors
  • Transforming Growth Factor beta