Evidence map›Paper›PMID 38514716›Full record

ArticleScientific reports2024

Single nuclei transcriptomics of the in situ human limbal stem cell niche.

Kathryn C Davidson, Minkyung Sung, Karl D Brown, Julian Contet, Serena Belluschi, Regan Hamel, Aida Moreno-Moral, Rodrigo L Dos Santos, Julian Gough, Jose M Polo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Recent Advances in Stem Cells of Corneal Epithelia.Investigative ophthalmology & visual science · 2025
    Review
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

Kathryn C Davidson *Department of Anatomy and Developmental Biology, Monash University, Clayton, VIC, Australia.
Minkyung Sung *Mogrify Limited, Cambridge, England, UK.
Karl D Brown *Centre for Eye Research Australia (CERA), Melbourne, Australia.
Julian ContetDepartment of Anatomy and Developmental Biology, Monash University, Clayton, VIC, Australia.
Serena BelluschiMogrify Limited, Cambridge, England, UK.
Regan HamelMogrify Limited, Cambridge, England, UK.
Aida Moreno-MoralMogrify Limited, Cambridge, England, UK.
Rodrigo L Dos SantosMogrify Limited, Cambridge, England, UK.
Julian GoughMogrify Limited, Cambridge, England, UK.
Jose M PoloDepartment of Anatomy and Developmental Biology, Monash University, Clayton, VIC, Australia. jose.polo@adelaide.edu.au.
Mark DaniellCentre for Eye Research Australia (CERA), Melbourne, Australia. daniellm@unimelb.edu.au.
Geraint J ParfittMogrify Limited, Cambridge, England, UK. geraint.parfitt@abbvie.com.
Centre for Eye Research Australia · AUMonash University · AUAbbVie (United States) · USMRC Laboratory of Molecular Biology · GBSouth Australian Health and Medical Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The corneal epithelium acts as a barrier to pathogens entering the eye; corneal epithelial cells are continuously renewed by uni-potent, quiescent limbal stem cells (LSCs) located at the limbus, where the cornea transitions to conjunctiva. There has yet to be a consensus on LSC markers and their transcriptome profile is not fully understood, which may be due to using cadaveric tissue without an intact stem cell niche for transcriptomics. In this study, we addressed this problem by using single nuclei RNA sequencing (snRNAseq) on healthy human limbal tissue that was immediately snap-frozen after excision from patients undergoing cataract surgery. We identified the quiescent LSCs as a sub-population of corneal epithelial cells with a low level of total transcript counts. Moreover, TP63, KRT15, CXCL14, and ITGβ4 were found to be highly expressed in LSCs and transiently amplifying cells (TACs), which constitute the corneal epithelial progenitor populations at the limbus. The surface markers SLC6A6 and ITGβ4 could be used to enrich human corneal epithelial cell progenitors, which were also found to specifically express the putative limbal progenitor cell markers MMP10 and AC093496.1.

Indexed as

Epithelium, CornealLimbus CorneaeCorneaGene Expression ProfilingHumansLimbal Stem CellsStem Cell Niche

Identifiers

PMID38514716
PMCPMC10957941
OpenAlexW4393051811

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.