Evidence map›Paper›PMID 21373883›Full record

ArticleStem cell reviews and reports2011

Re-assessing K15 as an epidermal stem cell marker.

Tammy-Claire Troy, Azadeh Arabzadeh, Kursad Turksen

Abstract read
PubMed Publisher
In one paragraph

Article in Stem cell reviews and reports, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.9field-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

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Frontiers in bioengineering and biotechnology · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Markers of epidermal stem cell subpopulations in adult mammalian skin.Cold Spring Harbor perspectives in medicine · 2014
    Review
  12. Article
  13. Article
  14. Keratin k15 as a biomarker of epidermal stem cells.International journal of molecular sciences · 2013
    Review
  15. Review
  16. Article
  17. Epidermal stem cell dynamics.Stem cell research & therapy · 2011
    Article
  18. Deregulation of epidermal stem cell niche contributes to pathogenesis of nonhealing venous ulcers.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    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

3 authors at 2 institutions in 1 country.

Tammy-Claire TroyRegenerative Medicine Program, Sprott Centre for Stem Cell Research at the Ottawa Hospital Research Institute, 501 Smyth Road-CCW5226, Ottawa, Ontario K1Y 8L6, Canada. ttroy@ohri.ca
Azadeh Arabzadeh
Kursad Turksen
Ottawa Hospital Research InstituteOttawa Hospital · CA

Funding

Canadian Institutes of Health Research MOP 84464
6 · The paper itself

Abstract

The intermediate filament keratin 15 (K15) is present in variable amounts in various stratified epithelia, but has also been reported to be a stem cell marker in the hair follicle. Using peptide specific antibodies, we evaluated the temporal and spatial distribution pattern of K15 expression/localization during normal epidermal development and initiation of hair follicle formation, and in the injured mature epidermis (e.g., during acute injury and repair and in tumorigenesis). During development, K15 expression is first localized to a subset of epidermal basal cells and the overlying periderm at E12.5, but its expression is seen throughout the basal layer by E15.5 and beyond. In hair follicle morphogenesis, initial peg formation occurs in a K15-null area at E14.5 and as peg elongation proceeds through to the mature hair follicle, K15 expression follows the leading edge with positive cells restricted to the outer root sheath. In an epidermal injury model, K15 is first up-regulated and associated with both the basal and suprabasal layers of the interfollicular epidermis then expression becomes sporadic and down-regulated before a basal layer-specific association is re-established in the repaired epidermis. During tumorigenesis, K15 is first mis-expressed, and is ultimately down-regulated. Our data suggest that K15 protein expression may reflect not only expression in a stem or progenitor cell subpopulation, but also reflects the activity and responsiveness of basal-like cells to loss of homeostasis of the epidermal differentiation program. Thus, the data suggest caution in using K15 alone to delineate epidermal stem cells, and underscore the need for further investigation of K15 and other markers in epidermal cell subpopulations.

Indexed as

9,10-Dimethyl-1,2-benzanthraceneAnimalsBiomarkersCell DifferentiationEmbryo, MammalianEmbryonic DevelopmentEpidermisGene Expression Regulation, NeoplasticHomeostasisKeratin-15MiceSkin NeoplasmsStem CellsTetradecanoylphorbol AcetateTime Factors9,10-Dimethyl-1,2-benzanthraceneBiomarkersKeratin-15Krt15 protein, mouseTetradecanoylphorbol Acetate

Identifiers

PMID21373883
OpenAlexW2094273655

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.