Evidence map›Paper›PMID 12079505›Full record

ArticleBMC immunology2002

Transcriptional response of human mast cells stimulated via the Fc(epsilon)RI and identification of mast cells as a source of IL-11.

Koichi Sayama, Maximilian Diehn, Kentaro Matsuda, Carolina Lunderius, Mindy Tsai, See-Ying Tam, David Botstein, Patrick O Brown, Stephen J Galli

Open access · goldAbstract read
In one paragraph

Article in BMC immunology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Exploring Mast Cell-CD8 T Cell Interactions in Inflammatory Skin Diseases.International journal of molecular sciences · 2023
    Review
  3. Mast Cells and Interleukins.International journal of molecular sciences · 2022
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. IL-17F-induced IL-11 release in bronchial epithelial cells via MSK1-CREB pathway.American journal of physiology. Lung cellular and molecular physiology · 2009
    Article
  14. Article
  15. Article
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  18. Article
  19. Article
  20. Mast cells enhance T cell activation: Importance of mast cell-derived TNF.Proceedings of the National Academy of Sciences of the United States of America · 2005
    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

9 authors at 2 institutions in 1 country.

Koichi SayamaDepartment of Pathology, Stanford University School of Medicine, Stanford, California, USA. aat99110@par.odn.ne.jp
Maximilian Diehn
Kentaro Matsuda
Carolina Lunderius
Mindy Tsai
See-Ying Tam
David Botstein
Patrick O Brown
Stephen J Galli
Stanford University · USHoward Hughes Medical Institute · US

Funding

A CANCER TAXONOMY BASED ON GENE EXPRESSION PATTERNSU01CA085129 · NCI · STANFORD UNIVERSITY · PI BROWN, PATRICK O. · 1999 to 2003
$8.5M
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
INITIATION/PERPETUATION OF ALLERGIC RESPONSES &ASTHMAU19AI041995 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KINET, JEAN-PIERRE M · 1997 to 2000
$812k
NCI NIH HHS CA 72074NCI NIH HHS CA 85129NCI NIH HHS R01 CA072074NCI NIH HHS U01 CA085129NHLBI NIH HHS HL 67674NHLBI NIH HHS P01 HL067674NHLBI NIH HHS P50 HL067674NIAID NIH HHS AI 23990NIAID NIH HHS AI 41995NIAID NIH HHS R01 AI023990NIAID NIH HHS R37 AI023990
6 · The paper itself

Abstract

backgroundIn asthma and other allergic disorders, the activation of mast cells by IgE and antigen induces the cells to release histamine and other mediators of inflammation, as well as to produce certain cytokines and chemokines. To search for new mast cell products, we used complementary DNA microarrays to analyze gene expression in human umbilical cord blood-derived mast cells stimulated via the high-affinity IgE receptor (Fc(epsilon)RI).

resultsOne to two hours after Fc(epsilon)RI-dependent stimulation, more than 2,400 genes (about half of which are of unknown function) exhibited 2-200 fold changes in expression. The transcriptional program included changes in the expression of IL-11 and at least 30 other cytokines and chemokines. Human mast cells secreted 130-529 pg of IL-11/106 cells by 6 h after stimulation with anti-IgE.

conclusionOur initial analysis of the transcriptional program induced in in vitro-derived human mast cells stimulated via the Fc(epsilon)RI has identified many products that heretofore have not been associated with this cell type, but which may significantly influence mast cell function in IgE-associated host responses. We also have demonstrated that mast cells stimulated via the Fc(epsilon)RI can secrete IL-11. Based on the previously reported biological effects of IL-11, our results suggest that production of IL-11 may represent one link between IgE-dependent mast cell activation in subjects with allergic asthma and the development of a spectrum of structural changes in the airways of these individuals; such changes, collectively termed "airway remodeling," can constitute an important long term consequence of asthma.

Indexed as

Antibodies, Anti-IdiotypicCells, CulturedGene Expression RegulationHistamine ReleaseHumansImmunoglobulin EInterleukin-11Interleukin-4Mast CellsOligonucleotide Array Sequence AnalysisReceptors, IgETranscription, GeneticAntibodies, Anti-IdiotypicImmunoglobulin EInterleukin-11Interleukin-4Receptors, IgE

Identifiers

PMID12079505
PMCPMC116674
OpenAlexW2143466612

What OpenQuestion holds

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Registered trials

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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.