# Single-Cell RNA-Seq Reveals Conserved Cellular Communication Mechanisms Governing Ocular Lineage Specification from Human iPS Cells

**Authors:** Laura Howard, Yuki Ishikawa, Rei Kamuro, Tomohiko Katayama, Kiranjit K. Bains, Matthew J. Hill, Derek J. Blake, Sung-Joon Park, Ryuhei Hayashi, Andrew J. Quantock, Kohji Nishida

PMC · DOI: 10.3390/cells15020104 · Cells · 2026-01-07

## TL;DR

This study uses single-cell RNA sequencing to uncover how human stem cells develop into eye-like structures, revealing conserved signaling pathways involved in eye development.

## Contribution

The study identifies conserved signaling mechanisms in ocular lineage specification using hiPSC-derived organoids.

## Key findings

- Key signaling pathways like Activin, FGF, BMP, WNT, and retinoic acid are active during ocular differentiation.
- Transcriptional regulators show conserved tissue-specific activity in eye development.
- hiPSC-derived organoids model early eye development and cellular communication effectively.

## Abstract

The complexity of cell fate decisions that underpin early eye development can be effectively modelled by leveraging the unique properties of human induced pluripotent stem cells (hiPSCs). In this study, we have utilised transcriptomic data generated from hiPSCs as they begin to self-organise and differentiate into two-dimensional eye-like organoids in vitro, and employ advanced single-cell analytical tools to dissect the cellular communication networks that direct this dynamic process. We have identified key signalling mediators and transcriptional effectors that guide the transition from pluripotency through to ocular differentiation, and our analyses reveal the conservation of developmentally defined signalling pathways. Members of the Activin, FGF, BMP, WNT, and retinoic acid families of ligands and receptors displayed communication probabilities consistent with their ocular-specific developmental roles in vivo, and this was accompanied by conserved tissue-specific activity of transcriptional regulators. These findings not only highlight the utility of hiPSCs for studying the cellular interactions and molecular pathways that drive early developmental decisions, but also advance our understanding of eye development in an accessible stem cell-based system.

## Linked entities

- **Chemicals:** Activin (PubChem CID 4435), BMP (PubChem CID 135538688), WNT (PubChem CID 24740085), retinoic acid (PubChem CID 444795)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** BMP1 (bone morphogenetic protein 1) [NCBI Gene 649] {aka OI13, PCOLC, PCP, TLD}, INHBE (inhibin subunit beta E) [NCBI Gene 83729]
- **Chemicals:** retinoic acid (MESH:D014212)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12839081/full.md

## References

100 references — full list in the complete paper: https://tomesphere.com/paper/PMC12839081/full.md

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Source: https://tomesphere.com/paper/PMC12839081