Evidence map›Paper›PMID 20100931›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

CD72 negatively regulates KIT-mediated responses in human mast cells.

Tatsuki R Kataoka, Atsushi Kumanogoh, Geethani Bandara, Dean D Metcalfe, Alasdair M Gilfillan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Strategies for Mast Cell Inhibition in Food Allergy.The Yale journal of biology and medicine · 2020
    Review
  5. Review
  6. Article
  7. Review
  8. CD100 Effects in Macrophages and Its Roles in Atherosclerosis.Frontiers in cardiovascular medicine · 2018
    Review
  9. Article
  10. Article
  11. Article
  12. Novel identified receptors on mast cells.Frontiers in immunology · 2012
    Article
  13. Article
  14. Review
  15. Regulation of mast cell responses in health and disease.Critical reviews in immunology · 2011
    Review
  16. Mast cells.Current gastroenterology reports · 2010
    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

5 authors at 2 institutions in 2 countries.

Tatsuki R KataokaLaboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. trkataoka@yahoo.co.jp
Atsushi Kumanogoh
Geethani Bandara
Dean D Metcalfe
Alasdair M Gilfillan
National Institutes of Health · USMicrobial Chemistry Research Foundation · JP

Funding

Critical signaling nodes regulating mast cell releasibility phenotypesZIAAI000967 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI METCALFE, DEAN D · 2009 to 2012
$1.4M
Molecular Biology Of Mast Cell Growth And DifferentiationZIAAI000513 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI METCALFE, DEAN D · 2009 to 2012
$1.3M
Intramural NIH HHS ZIA AI000967
6 · The paper itself

Abstract

KIT activation, through binding of its ligand, stem cell factor, is crucial for normal mast cell growth, differentiation, and survival. Furthermore, KIT may also contribute to mast cell homing and cytokine generation. Activating mutations in KIT lead to the dysregulated mast cell growth associated with the myeloproliferative disorder, mastocytosis. We investigated the potential of downregulating such responses through mast cell inhibitory receptor activation. In this study, we report that the B cell-associated ITIM-containing inhibitory receptor, CD72, is expressed in human mast cells. Ligation of CD72 with the agonistic Ab, BU40, or with recombinant human CD100 (rCD100), its natural ligand, induced the phosphorylation of CD72 with a resulting increase in its association with the tyrosine phosphatase SH2 domain-containing phosphatase-1. This, in turn, resulted in an inhibition of KIT-induced phosphorylation of Src family kinases and extracellular-regulated kinases (ERK1/2). As a consequence of these effects, KIT-mediated mast cell proliferation, chemotaxis, and chemokine production were significantly reduced by BU40 and rCD100. Furthermore, BU40 and rCD100 also downregulated the growth of the HMC1.2 human mast cell line. Thus, targeting CD72 may provide a novel approach to the suppression of mast cell disease such as mastocytosis.

Indexed as

Antibodies, MonoclonalAntigens, CDAntigens, Differentiation, B-LymphocyteBlotting, WesternCell CycleCell DegranulationCell Line, TumorCell ProliferationCells, CulturedChemokine CCL2ChemotaxisFlow CytometryHumansMast CellsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Antibodies, MonoclonalAntigens, CDAntigens, Differentiation, B-LymphocyteCCL2 protein, humanCD100 antigenCD72 protein, humanChemokine CCL2Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Protein Tyrosine Phosphatase, Non-Receptor Type 6Proto-Oncogene Proteins c-kitReceptors, IgERecombinant ProteinsSemaphorinsStem Cell Factor

Identifiers

PMID20100931
PMCPMC2824776
OpenAlexW2163791365

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.