Evidence map›Paper›PMID 23932072›Full record

ArticleThe Journal of allergy and clinical immunology2013

Histamine induces proliferation in keratinocytes from patients with atopic dermatitis through the histamine 4 receptor.

Franziska Glatzer, Maria Gschwandtner, Sarah Ehling, Kristine Rossbach, Katrin Janik, Andreas Klos, Wolfgang Bäumer, Manfred Kietzmann, Thomas Werfel, Ralf Gutzmer

Abstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

32 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Critical Players and Therapeutic Targets in Chronic Itch.International journal of molecular sciences · 2022
    Review
  6. Type 2 Inflammation Contributes to Skin Barrier Dysfunction in Atopic Dermatitis.JID innovations : skin science from molecules to population health · 2022
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. The Implications of Pruritogens in the Pathogenesis of Atopic Dermatitis.International journal of molecular sciences · 2021
    Review
  13. Production of IL-31 in CD45ROJournal of clinical medicine · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Intracellular CaInternational journal of molecular sciences · 2020
    Article
  18. Article
  19. The role of the histamine HBritish journal of pharmacology · 2020
    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

10 authors at 3 institutions in 2 countries.

Franziska GlatzerDivision of Immunodermatology and Allergy Research, Department of Dermatology and Allergy, Hannover Medical School, Hannover, Germany. Electronic address: Glatzer.Franziska@mh-hannover.de.
Maria Gschwandtner
Sarah Ehling
Kristine Rossbach
Katrin Janik
Andreas Klos
Wolfgang Bäumer
Manfred Kietzmann
Thomas Werfel
Ralf Gutzmer
Medizinische Hochschule Hannover · DEUniversity of Veterinary Medicine Hannover, Foundation · DEUniversity of Veterinary Medicine Vienna · AT

Funding

Austrian Science Fund FWF T 545
6 · The paper itself

Abstract

backgroundEpidermal hyperproliferation resulting in acanthosis is an important clinical observation in patients with atopic dermatitis, and its underlying mechanisms are not completely understood.

objectiveBecause increased levels of histamine are present in lesional skin, we investigated the effect of histamine, especially with regard to histamine 4 receptor (H4R) activation, on the proliferation of human and murine keratinocytes.

methodsThe expression of H4R on human and murine keratinocytes was detected by using real-time PCR. Keratinocyte proliferation was evaluated by using different in vitro cell proliferation assays, scratch assays, and measurement of the epidermal thickness of murine skin.

resultsWe detected H4R mRNA on foreskin keratinocytes and on outer root sheath keratinocytes; H4R mRNA was more abundant in keratinocytes from patients with atopic dermatitis compared with those from nonatopic donors. Stimulation of foreskin keratinocytes, atopic dermatitis outer root sheath keratinocytes, and H4R-transfected HaCaT cells with histamine and H4R agonist resulted in an increase in proliferation, which was blocked with the H4R-specific antagonist JNJ7777120. Abdominal epidermis of H4R-deficient mice was significantly thinner, and the in vitro proliferation of keratinocytes derived from H4R-deficient mice was lower compared with that seen in control mice. Interestingly, we only detected H4R expression on murine keratinocytes after stimulation with LPS and peptidoglycan.

conclusionH4R is highly expressed on keratinocytes from patients with atopic dermatitis, and its stimulation induces keratinocyte proliferation. This might represent a mechanism that contributes to the epidermal hyperplasia observed in patients with atopic dermatitis.

Indexed as

AnimalsCell LineCell ProliferationDermatitis, AtopicFemaleGene Expression RegulationHistamineHistamine AntagonistsHumansIndolesKeratinocytesLipopolysaccharidesMaleMiceMice, Inbred BALB CPeptidoglycan1-((5-chloro-1H-indol-2-yl)carbonyl)-4-methylpiperazineHistamineHistamine AntagonistsHRH4 protein, humanHrh4 protein, mouseIndolesLipopolysaccharidesPeptidoglycanPiperazinesReceptors, G-Protein-CoupledReceptors, HistamineReceptors, Histamine H44-Methylhistamine4-MHatopic dermatitisGAPDHGlyceraldehyde-3-phosphate dehydrogenaseH1RH2RH3RH4RHistamineHistamine 1 receptorHistamine 2 receptorHistamine 3 receptorhistamine 4 receptorHistamine 4 receptorhumankeratinocytemouseNeonatal keratinocytenKCorsKCOuter root sheath keratinocyteproliferation

Identifiers

PMID23932072
PMCPMC4447893
OpenAlexW2018126926

What OpenQuestion holds

Textmetadata
LicenceTDM
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.