Mouse Model of Sutured Endothelial Keratoplasty Technique.

Background/

Objectives

In this study, a mouse model of sutured endothelial keratoplasty was established and compared with a traditional penetrating keratoplasty (PKP) model in both syngeneic (BALB/c) and allogeneic (C57/BL6) patterns.

Methods

For the endothelial keratoplasty (EK) model, chimeric donor tissues consisting of BALB/c epithelium-stroma combined with either syngeneic (BALB/c) or allogeneic (C57/BL6) stroma-endothelium were transplanted into BALB/c mice. Graft transparency, gene expression, and mRNA levels in the transplanted tissues were assessed using polymerase chain reaction (PCR) and quantitative real-time reverse transcription PCR (qRT-PCR) to evaluate inflammatory status.

Results

Allogeneic PKP had a higher opacity score than syngeneic PKP. In contrast, syngeneic EK mice had similar opacity scores to those of allogeneic EK mice. Upregulation of CXCR3, the receptor for CXCL10, was demonstrated by qRT-PCR in allogeneic PKP mice but not in allogeneic EK mice.

Conclusions

Comparison between the syngeneic and allogeneic PKP groups revealed differences in CXCR3 mRNA expression, suggesting that CXCR3 could be a potential biomarker for rejection in the PKP mouse model. Additionally, the EK model did not show CXCR3 upregulation despite the opaque cornea due to nonspecific inflammation. Therefore, our mouse model was considered to be a successfully established EK model.