Evidence map›Paper›PMID 24936454›Full record

ArticleStem cell reports2014

3D In vitro model of a functional epidermal permeability barrier from human embryonic stem cells and induced pluripotent stem cells.

Anastasia Petrova, Anna Celli, Laureen Jacquet, Dimitra Dafou, Debra Crumrine, Melanie Hupe, Matthew Arno, Carl Hobbs, Aleksandra Cvoro, Panagiotis Karagiannis and 7 more

Abstract read
In one paragraph

Article in Stem cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
–field-weighted citation impact
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

50 citing papers in PubMed.

  1. Article
  2. Review
  3. Cytosine Deaminase Base Editing to RestoreJID innovations : skin science from molecules to population health · 2023
    Article
  4. Interactions betweenInternational journal of molecular sciences · 2023
    Article
  5. Article
  6. Review
  7. Epidermal Basement Membrane Substitutes for Bioengineering of Human Epidermal Equivalents.JID innovations : skin science from molecules to population health · 2022
    Article
  8. mRNA-Based Reprogramming Under Xeno-Free and Feeder-Free Conditions.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

17 authors.

Anastasia PetrovaStem Cell Laboratory, Assisted Conception Unit, Division of Women's Health, Women's Health Academic Centre, King's College London, London SE1 9RT, UK ; St John's Institute of Dermatology, King's College London, London SE1 9RT, UK.
Anna CelliDepartment of Dermatology, Veteran Affairs Medical Center, University of California, San Francisco, San Francisco, CA 94121, USA.
Laureen JacquetStem Cell Laboratory, Assisted Conception Unit, Division of Women's Health, Women's Health Academic Centre, King's College London, London SE1 9RT, UK.
Dimitra DafouDivision of Genetics and Molecular Medicine, King's College London School of Medicine, Guy's Hospital, London SE1 9RT, UK.
Debra CrumrineDepartment of Dermatology, Veteran Affairs Medical Center, University of California, San Francisco, San Francisco, CA 94121, USA.
Melanie HupeDepartment of Dermatology, Veteran Affairs Medical Center, University of California, San Francisco, San Francisco, CA 94121, USA.
Matthew ArnoGenomics Centre, King's College London, London SE1 9NH, UK.
Carl HobbsHistology Laboratory, Wolfson Centre for Age-Related Diseases, School of Biomedical Sciences, King's College London, London SE1 1UL, UK.
Aleksandra CvoroGenomic Medicine, The Methodist Hospital Research Institute, Houston, TX 77030, USA.
Panagiotis KaragiannisSt John's Institute of Dermatology, King's College London, London SE1 9RT, UK.
Liani DevitoStem Cell Laboratory, Assisted Conception Unit, Division of Women's Health, Women's Health Academic Centre, King's College London, London SE1 9RT, UK.
Richard SunDepartment of Dermatology, Veteran Affairs Medical Center, University of California, San Francisco, San Francisco, CA 94121, USA.
Lillian C AdameDepartment of Dermatology, Veteran Affairs Medical Center, University of California, San Francisco, San Francisco, CA 94121, USA.
Robert VaughanClinical Transplantation Laboratory, GSTS and MRC Centre for Transplantation, King's College London, King's Health Partners, London SE1 9RT, UK.
John A McGrathSt John's Institute of Dermatology, King's College London, London SE1 9RT, UK.
Theodora M MauroDepartment of Dermatology, Veteran Affairs Medical Center, University of California, San Francisco, San Francisco, CA 94121, USA.
Dusko IlicStem Cell Laboratory, Assisted Conception Unit, Division of Women's Health, Women's Health Academic Centre, King's College London, London SE1 9RT, UK.

Funding

ATP2A2-Regulated Keretinocyted Ca2+ Signaling MechanismsR01AR051930 · NIAMS · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI MAURO, THEODORA M · 2006 to 2019
$3.2M
The Lipid and Tight Junction Epidermal Barriers are InterdependentR21AR061583 · NIAMS · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI MAURO, THEODORA M · 2012 to 2013
$358k
Medical Research Council G0701172Medical Research Council G0801061Medical Research Council GO801061NIAMS NIH HHS R01 AR051930NIAMS NIH HHS R21 AR061583PHS HHS R21 ARO61583
6 · The paper itself

Abstract

Cornification and epidermal barrier defects are associated with a number of clinically diverse skin disorders. However, a suitable in vitro model for studying normal barrier function and barrier defects is still lacking. Here, we demonstrate the generation of human epidermal equivalents (HEEs) from human embryonic stem cells (hESCs) and induced pluripotent stem cells (iPSCs). HEEs are structurally similar to native epidermis, with a functional permeability barrier. We exposed a pure population of hESC/iPSC-derived keratinocytes, whose transcriptome corresponds to the gene signature of normal primary human keratinocytes (NHKs), to a sequential high-to-low humidity environment in an air/liquid interface culture. The resulting HEEs had all of the cellular strata of the human epidermis, with skin barrier properties similar to those of normal skin. Such HEEs generated from disease-specific iPSCs will be an invaluable tool not only for dissecting molecular mechanisms that lead to epidermal barrier defects but also for drug development and screening.

Indexed as

Models, BiologicalCell Culture TechniquesCell DifferentiationCells, CulturedCellular ReprogrammingDNA MethylationEmbryonic Stem CellsEpidermisEpithelial-Mesenchymal TransitionHumansInduced Pluripotent Stem CellsKeratin-14KeratinocytesPermeabilityPrincipal Component AnalysisTeratomaKeratin-14KRT14 protein, humanTranscription Factors

Identifiers

PMID24936454
PMCPMC4050479

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.