ArticleCornea2026
Single-Cell RNA Sequencing of Murine Limbal Epithelia Reveals Gas1 as a Novel Stem/Progenitor Cell Marker for the Corneal Epithelium.
Article in Cornea, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
1 citing paper in PubMed.
- In situ spatial transcriptomics reveals novel markers of the limbal stem cell niche and ocular surface epithelia.Stem cell reports · 2026Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
purposeThe corneal epithelium is endowed with a rare population of stem cells that reside within the limbus, a circumferential transition zone that partitions the cornea from the conjunctiva. These cells are thus referred to as limbal epithelial stem cells. Despite the surge in investigations using single-cell RNA sequencing (scRNA-seq) of the ocular surface, a unifying marker(s) that distinguishes these cells from their progeny is yet to be identified.
methodsWe used a keratin (K)-14-driven lineage-tracing system and SmartSeq-2 single-cell transcriptomics in 5- to 60-week-old mice to interrogate the identity of limbal epithelia. These results were then validated using flow cytometry, immunofluorescence, and a central corneal injury model.
resultsFour cell clusters were identified, derived from both Confetti + and Confetti - cells (clusters 0-3), with cluster 3 designated as harboring progenitor cells. We focused on one gene of interest in cluster 3, growth arrest-specific gene 1 ( Gas1 ), which codes for a cell-surface protein. PCR, flow cytometry, and immunofluorescence revealed that this gene is expressed in a rare population of limbal epithelial cells. Gas1 was also coexpressed with K14 in both young and old mice and upregulated after a mild mechanical debridement injury to the central cornea.
conclusionsThe cell-surface expression of this protein can be used to identify, extract, and enrich progenitor cells for downstream molecular investigations and for generating better-quality cell-based grafts to treat severe corneal disease.
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