Evidence map›Paper›PMID 23962810›Full record

ArticleThe Journal of investigative dermatology2014

Keratin 9 is required for the structural integrity and terminal differentiation of the palmoplantar epidermis.

Dun Jack Fu, Calum Thomson, Declan P Lunny, Patricia J Dopping-Hepenstal, John A McGrath, Frances J D Smith, W H Irwin McLean, Deena M Leslie Pedrioli

Open access · hybridAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

52 citing papers in PubMed, 88 citations in OpenAlex.

  1. Physiological and Proteomic Responses to Chronic Stress and the Effects ofAnimals : an open access journal from MDPI · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Review
  8. Keratin isoform shifts modulate motility signals during wound healing.bioRxiv : the preprint server for biology · 2024
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Type 2 Inflammation Contributes to Skin Barrier Dysfunction in Atopic Dermatitis.JID innovations : skin science from molecules to population health · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. From structural resilience to cell specification - Intermediate filaments as regulators of cell fate.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Review
  18. Article
  19. Article
  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

8 authors at 3 institutions in 2 countries.

Dun Jack FuDivision of Molecular Medicine and Centre for Dermatology and Genetic Medicine, Colleges of Life Sciences and Medicine, Dentistry and Nursing, University of Dundee, Dundee, UK.
Calum ThomsonMicroscopy Facility, College of Life Sciences, University of Dundee, Dundee, UK.
Declan P LunnyEpithelial Biology Group, Institute of Medical Biology, Immunos, Singapore.
Patricia J Dopping-HepenstalGuy's and St Thomas' (GSTS) Pathology, St Thomas' Hospital, London, UK.
John A McGrathSt John's Institute of Dermatology, King's College London, London, UK.
Frances J D SmithDivision of Molecular Medicine and Centre for Dermatology and Genetic Medicine, Colleges of Life Sciences and Medicine, Dentistry and Nursing, University of Dundee, Dundee, UK.
W H Irwin McLeanDivision of Molecular Medicine and Centre for Dermatology and Genetic Medicine, Colleges of Life Sciences and Medicine, Dentistry and Nursing, University of Dundee, Dundee, UK.
Deena M Leslie PedrioliDivision of Molecular Medicine and Centre for Dermatology and Genetic Medicine, Colleges of Life Sciences and Medicine, Dentistry and Nursing, University of Dundee, Dundee, UK. Electronic address: d.lesliepedrioli@dundee.ac.uk.
University of Dundee · GBInstitute of Medical Biology · SGKing's College London · GB

Funding

Medical Research Council G0801742Medical Research Council G0802780Wellcome Trust 098439Wellcome Trust 098439/Z/12/Z
6 · The paper itself

Abstract

Keratin 9 (K9) is a type I intermediate filament protein whose expression is confined to the suprabasal layers of the palmoplantar epidermis. Although mutations in the K9 gene are known to cause epidermolytic palmoplantar keratoderma, a rare dominant-negative skin disorder, its functional significance is poorly understood. To gain insight into the physical requirement and importance of K9, we generated K9-deficient (Krt9(-/-)) mice. Here, we report that adult Krt9(-/-)mice develop calluses marked by hyperpigmentation that are exclusively localized to the stress-bearing footpads. Histological, immunohistochemical, and immunoblot analyses of these regions revealed hyperproliferation, impaired terminal differentiation, and abnormal expression of keratins K5, K14, and K2. Furthermore, the absence of K9 induces the stress-activated keratins K6 and K16. Importantly, mice heterozygous for the K9-null allele (Krt9(+/-)) show neither an overt nor histological phenotype, demonstrating that one Krt9 allele is sufficient for the developing normal palmoplantar epidermis. Together, our data demonstrate that complete ablation of K9 is not tolerable in vivo and that K9 is required for terminal differentiation and maintaining the mechanical integrity of palmoplantar epidermis.

Indexed as

Age FactorsAnimalsCell DifferentiationCell ProliferationCytoskeletonDisease Models, AnimalEpidermisHyperpigmentationKeratin-9Keratoderma, Palmoplantar, EpidermolyticMiceMice, Inbred C57BLMice, KnockoutPhenotypeRNA, Small InterferingKeratin-9KRT9 protein, mouseRNA, Small Interfering

Identifiers

PMID23962810
PMCPMC3923277
OpenAlexW2027845234

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.