Evidence map›Paper›PMID 17071594›Full record

ArticleThe American journal of pathology2006

Mast cell-derived tumor necrosis factor can promote nerve fiber elongation in the skin during contact hypersensitivity in mice.

Maki Kakurai, Rossella Monteforte, Hajime Suto, Mindy Tsai, Susumu Nakae, Stephen J Galli

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. 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
2.1field-weighted citation impact, top 13% 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, 88 citations in OpenAlex.

  1. Article
  2. Skin innervation and itsFrontiers in cellular neuroscience · 2026
    Review
  3. Article
  4. Roles of Mast Cells in Cutaneous Diseases.Frontiers in immunology · 2022
    Review
  5. Mast Cells in the Skin: Defenders of Integrity or Offenders in Inflammation?International journal of molecular sciences · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. The Dynamics of the Skin's Immune System.International journal of molecular sciences · 2019
    Review
  11. Neuro-immune crosstalk and allergic inflammation.The Journal of clinical investigation · 2019
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Molecular and cellular mechanisms that initiate pain and itch.Cellular and molecular life sciences : CMLS · 2015
    Review
  18. Article
  19. Mast cells: versatile gatekeepers of pain.Molecular immunology · 2015
    Review
  20. Mechanisms underlying the neuronal-based symptoms of allergy.The Journal of allergy and clinical immunology · 2014
    Review
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

6 authors at 2 institutions in 2 countries.

Maki KakuraiDepartment of Pathology, L-235, Stanford University School of Medicine, 300 Pasteur Dr., Stanford, CA 94305-5324, USA.
Rossella Monteforte
Hajime Suto
Mindy Tsai
Susumu Nakae
Stephen J Galli
Stanford University · USStanford Medicine · US

Funding

SCOR in Cellular and Molecular Mechanisms of AsthmaP50HL067674 · NHLBI · STANFORD UNIVERSITY · PI VAN DE RIJN, JAN MATT · 2002 to 2005
$4.8M
Role of Mast Cells in Inflammation and ImmunityR01CA072074 · NCI · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 1996 to 2010
$4.4M
Regulation of Mast Cell Development and FunctionR01AI023990 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 1986 to 2010
$2.4M
REGULATION OF MAST CELL DEVELOPMENT &FUNCTIONR37AI023990 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN J · 1996 to 2005
$2.2M
SCOR in Cellular and Molecular Mechanisms of AsthmaP01HL067674 · NHLBI · STANFORD UNIVERSITY · PI GALLI, STEPHEN J · 2001 to 2001
$1.2M
NCI NIH HHS CA72074NCI NIH HHS R01 CA072074NHLBI NIH HHS HL67674NHLBI NIH HHS P01 HL067674NHLBI NIH HHS P50 HL067674NIAID NIH HHS AI23990NIAID NIH HHS R01 AI023990NIAID NIH HHS R37 AI023990
6 · The paper itself

Abstract

In humans, lesions of contact eczema or atopic dermatitis can exhibit increases in epidermal nerves, but the mechanism resulting in such nerve elongation are not fully understood. We found that contact hypersensitivity reactions to oxazolone in mice were associated with significant increases in the length of nerves in the epidermis and dermis. Using genetically mast cell-deficient c-kit mutant mice selectively repaired of their dermal mast cell deficiency with either wild-type or tumor necrosis factor (TNF)-deficient mast cells, we found that mast cells, and mast cell-derived TNF, significantly contributed to the elongation of epidermal and dermal PGP 9.5+ nerves and dermal CGRP+ nerves, as well as to the inflammation observed at sites of contact hypersensitivity in response to oxazolone. Moreover, the percentage of mast cells in close proximity to dermal PGP 9.5+ nerve fibers was significantly higher in wild-type mice and in c-kit mutant mice repaired of their dermal mast cell deficiency by the adoptive transfer of wild-type mast cells than in TNF-deficient mice or in TNF-/- mast cell-engrafted c-kit mutant mice. These observations show that mast cells, and mast cell-derived TNF, can promote the elongation of cutaneous nerve fibers during contact hypersensitivity in the mouse.

Indexed as

AnimalsDermatitis, ContactEarMast CellsMiceMice, Inbred C57BLNerve FibersOxazoloneSkinTumor Necrosis FactorsOxazoloneTumor Necrosis Factors

Identifiers

PMID17071594
PMCPMC1780201
OpenAlexW1999366816

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.