# Patient-Derived Immortalized Limbal Epithelial Cells as In Vitro Models of Congenital Aniridia

**Authors:** Tanja Stachon, Shweta Suiwal, Virendra Kumar, Tobias May, Frank Schmitz, Maryam Amini, Fabian N. Fries, Berthold Seitz, Shao-Lun Hsu, Shuailin Li, Shanhe Liu, Swarnali Kundu, Nicole Ludwig, Nóra Szentmáry

PMC · DOI: 10.3390/cells15050394 · Cells · 2026-02-24

## TL;DR

Researchers created long-lasting lab cell models from patients with congenital aniridia to study the disease and test new treatments.

## Contribution

The study introduces patient-derived immortalized limbal epithelial cells as a novel in vitro model for PAX6-associated aniridia.

## Key findings

- Aniridia-derived cell lines showed reduced nuclear PAX6 immunosignals compared to controls.
- mRNA sequencing revealed over 14,000 transcripts, including unique subsets in aniridia-derived lines.
- Cell lines preserved epithelial characteristics and overall transcriptomic similarity to healthy controls.

## Abstract

Purpose: To establish and comprehensively characterize immortalized limbal epithelial cell lines derived from patients with PAX6 haploinsufficiency-associated congenital aniridia, as well as from a healthy donor. These well-defined cell models provide a reliable and reproducible platform for long-term experimental studies, facilitating mechanistic investigations and the development and evaluation of novel therapeutic approaches. Methods: Primary limbal epithelial cells were isolated from biopsies of two patients with distinct PAX6 variants and from a healthy donor. Immortalization was performed by InSCREENex GmbH. The resulting cell lines were characterized using microscopy, BrdU assay, qPCR, flow cytometry, immunocytochemistry, and mRNA sequencing. Results: Immortalized aniridia and control cell lines displayed typical polygonal epithelial morphology and comparable proliferation rates. Total PAX6 mRNA and protein levels were similar among groups; however, nuclear PAX6 immunosignals were significantly reduced in aniridia-derived lines. Expression of ABCG2, TP63, FOSL2, ALDH1A1, and FABP5 showed no significant differences, except for reduced ΔNp63α protein levels in one aniridia line. mRNA sequencing detected more than 14,000 transcripts, including subsets uniquely expressed in control and aniridia-derived lines. Conclusions: Immortalized aniridia limbal epithelial cell lines preserve key epithelial characteristics and overall transcriptomic similarity to controls while exhibiting disease-relevant molecular alterations. These cell lines represent models of PAX6-associated ocular surface disease.

## Linked entities

- **Genes:** PAX6 (paired box 6) [NCBI Gene 5080], ABCG2 (ATP binding cassette subfamily G member 2 (JR blood group)) [NCBI Gene 9429], TP63 (tumor protein p63) [NCBI Gene 8626], FOSL2 (FOS like 2, AP-1 transcription factor subunit) [NCBI Gene 2355], ALDH1A1 (aldehyde dehydrogenase 1 family member A1) [NCBI Gene 216], FABP5 (fatty acid binding protein 5) [NCBI Gene 2171]
- **Proteins:** PAX6 (paired box 6)

## Full-text entities

- **Genes:** ABCG2 (ATP binding cassette subfamily G member 2 (JR blood group)) [NCBI Gene 9429] {aka ABC15, ABCP, BCRP, BMDP, CD338, CDw338}, FABP5 (fatty acid binding protein 5) [NCBI Gene 2171] {aka E-FABP, EFABP, KFABP, PA-FABP, PAFABP}, ALDH1A1 (aldehyde dehydrogenase 1 family member A1) [NCBI Gene 216] {aka ALDC, ALDH-E1, ALDH1, ALDH11, HEL-9, HEL-S-53e}, PAX6 (paired box 6) [NCBI Gene 5080] {aka AN, AN1, AN2, ASGD5, D11S812E, FVH1}, TP63 (tumor protein p63) [NCBI Gene 8626] {aka AIS, B(p51A), B(p51B), EEC3, KET, LMS}, FOSL2 (FOS like 2, AP-1 transcription factor subunit) [NCBI Gene 2355] {aka ACED, FRA2}
- **Diseases:** Aniridia (MESH:D015783), ocular surface disease (MESH:D010534)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12984925/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12984925/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12984925/full.md

---
Source: https://tomesphere.com/paper/PMC12984925